---
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334386
feature_type: variation
id: rs2062363010
seq_region_name: 17
source: dbSNP
start: 73334386
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1360157671
seq_region_name: 17
source: dbSNP
start: 73334387
strand: 1
-
alleles:
- AAAAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs956678688
seq_region_name: 17
source: dbSNP
start: 73334387
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1022178326
seq_region_name: 17
source: dbSNP
start: 73334393
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs968120433
seq_region_name: 17
source: dbSNP
start: 73334394
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1441940109
seq_region_name: 17
source: dbSNP
start: 73334396
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363140
seq_region_name: 17
source: dbSNP
start: 73334402
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1412169014
seq_region_name: 17
source: dbSNP
start: 73334408
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs539403953
seq_region_name: 17
source: dbSNP
start: 73334411
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1473439043
seq_region_name: 17
source: dbSNP
start: 73334415
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363206
seq_region_name: 17
source: dbSNP
start: 73334417
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334418
feature_type: variation
id: rs1237518217
seq_region_name: 17
source: dbSNP
start: 73334418
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334427
feature_type: variation
id: rs967928483
seq_region_name: 17
source: dbSNP
start: 73334427
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334432
feature_type: variation
id: rs2062363256
seq_region_name: 17
source: dbSNP
start: 73334432
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363270
seq_region_name: 17
source: dbSNP
start: 73334433
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334434
feature_type: variation
id: rs2062363295
seq_region_name: 17
source: dbSNP
start: 73334434
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363312
seq_region_name: 17
source: dbSNP
start: 73334436
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1487073659
seq_region_name: 17
source: dbSNP
start: 73334437
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs975280790
seq_region_name: 17
source: dbSNP
start: 73334441
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2145351108
seq_region_name: 17
source: dbSNP
start: 73334442
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1216983919
seq_region_name: 17
source: dbSNP
start: 73334449
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1361108984
seq_region_name: 17
source: dbSNP
start: 73334454
strand: 1
-
alleles:
- AAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363432
seq_region_name: 17
source: dbSNP
start: 73334457
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1028725142
seq_region_name: 17
source: dbSNP
start: 73334458
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334460
feature_type: variation
id: rs955412688
seq_region_name: 17
source: dbSNP
start: 73334460
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1453308352
seq_region_name: 17
source: dbSNP
start: 73334462
strand: 1
-
alleles:
- TTTCTTTCTT
- TTTCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1355576122
seq_region_name: 17
source: dbSNP
start: 73334464
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363511
seq_region_name: 17
source: dbSNP
start: 73334467
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs3764369
seq_region_name: 17
source: dbSNP
start: 73334469
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs749283667
seq_region_name: 17
source: dbSNP
start: 73334473
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363613
seq_region_name: 17
source: dbSNP
start: 73334474
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs987423386
seq_region_name: 17
source: dbSNP
start: 73334475
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363686
seq_region_name: 17
source: dbSNP
start: 73334476
strand: 1
-
alleles:
- AAAAAA
- AAAA
- AAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1356677897
seq_region_name: 17
source: dbSNP
start: 73334485
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1398246348
seq_region_name: 17
source: dbSNP
start: 73334495
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363770
seq_region_name: 17
source: dbSNP
start: 73334496
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs566751969
seq_region_name: 17
source: dbSNP
start: 73334505
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1299031993
seq_region_name: 17
source: dbSNP
start: 73334506
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363846
seq_region_name: 17
source: dbSNP
start: 73334507
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363864
seq_region_name: 17
source: dbSNP
start: 73334509
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334511
feature_type: variation
id: rs1421818533
seq_region_name: 17
source: dbSNP
start: 73334511
strand: 1
-
alleles:
- ATA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs986949271
seq_region_name: 17
source: dbSNP
start: 73334516
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1164562061
seq_region_name: 17
source: dbSNP
start: 73334517
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334522
feature_type: variation
id: rs2062363926
seq_region_name: 17
source: dbSNP
start: 73334522
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062363951
seq_region_name: 17
source: dbSNP
start: 73334523
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs77678500
seq_region_name: 17
source: dbSNP
start: 73334525
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334526
feature_type: variation
id: rs1416613537
seq_region_name: 17
source: dbSNP
start: 73334526
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1599457102
seq_region_name: 17
source: dbSNP
start: 73334527
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs937157077
seq_region_name: 17
source: dbSNP
start: 73334528
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs974203360
seq_region_name: 17
source: dbSNP
start: 73334529
strand: 1
-
alleles:
- TTTTTTT
- TT
- TTTT
- TTTTTT
- TTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334535
feature_type: variation
id: rs973680060
seq_region_name: 17
source: dbSNP
start: 73334529
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs920851212
seq_region_name: 17
source: dbSNP
start: 73334531
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334538
feature_type: variation
id: rs2062364099
seq_region_name: 17
source: dbSNP
start: 73334538
strand: 1
-
alleles:
- ACAGACAGACA
- ACAGACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs3834965
seq_region_name: 17
source: dbSNP
start: 73334539
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334547
feature_type: variation
id: rs1055177846
seq_region_name: 17
source: dbSNP
start: 73334547
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334549
feature_type: variation
id: rs372202981
seq_region_name: 17
source: dbSNP
start: 73334549
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334550
feature_type: variation
id: rs2062364181
seq_region_name: 17
source: dbSNP
start: 73334550
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334552
feature_type: variation
id: rs3764368
seq_region_name: 17
source: dbSNP
start: 73334552
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334557
feature_type: variation
id: rs1045275934
seq_region_name: 17
source: dbSNP
start: 73334557
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334559
feature_type: variation
id: rs905350659
seq_region_name: 17
source: dbSNP
start: 73334559
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334560
feature_type: variation
id: rs1216798455
seq_region_name: 17
source: dbSNP
start: 73334560
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334562
feature_type: variation
id: rs2062364260
seq_region_name: 17
source: dbSNP
start: 73334562
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334565
feature_type: variation
id: rs1184776191
seq_region_name: 17
source: dbSNP
start: 73334565
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334567
feature_type: variation
id: rs1317365023
seq_region_name: 17
source: dbSNP
start: 73334567
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334574
feature_type: variation
id: rs1195875140
seq_region_name: 17
source: dbSNP
start: 73334574
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334576
feature_type: variation
id: rs567438894
seq_region_name: 17
source: dbSNP
start: 73334576
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334577
feature_type: variation
id: rs1278973299
seq_region_name: 17
source: dbSNP
start: 73334577
strand: 1
-
alleles:
- TTTTTT
- TTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334583
feature_type: variation
id: rs1245553882
seq_region_name: 17
source: dbSNP
start: 73334578
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334582
feature_type: variation
id: rs537951787
seq_region_name: 17
source: dbSNP
start: 73334582
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334584
feature_type: variation
id: rs939478453
seq_region_name: 17
source: dbSNP
start: 73334584
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334587
feature_type: variation
id: rs1293249220
seq_region_name: 17
source: dbSNP
start: 73334587
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334588
feature_type: variation
id: rs189126502
seq_region_name: 17
source: dbSNP
start: 73334588
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334588
feature_type: variation
id: rs1437640694
seq_region_name: 17
source: dbSNP
start: 73334588
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334590
feature_type: variation
id: rs1408981401
seq_region_name: 17
source: dbSNP
start: 73334590
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334592
feature_type: variation
id: rs2062364461
seq_region_name: 17
source: dbSNP
start: 73334592
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334596
feature_type: variation
id: rs2062364482
seq_region_name: 17
source: dbSNP
start: 73334596
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334600
feature_type: variation
id: rs1169159141
seq_region_name: 17
source: dbSNP
start: 73334600
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334601
feature_type: variation
id: rs2062364515
seq_region_name: 17
source: dbSNP
start: 73334601
strand: 1
-
alleles:
- AAAAAA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334606
feature_type: variation
id: rs1568353560
seq_region_name: 17
source: dbSNP
start: 73334601
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334603
feature_type: variation
id: rs2062364552
seq_region_name: 17
source: dbSNP
start: 73334603
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73334605
feature_type: variation
id: rs2062364570
seq_region_name: 17
source: dbSNP
start: 73334605
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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start: 73334810
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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source: dbSNP
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73334820
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73334824
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73334830
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335016
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335021
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335026
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335028
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73335030
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335034
strand: 1
-
alleles:
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- CTTTTTCT
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335035
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335038
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335042
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335054
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335057
strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335059
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335071
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73335071
strand: 1
-
alleles:
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- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73335072
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335074
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id: rs750340945
seq_region_name: 17
source: dbSNP
start: 73335074
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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-
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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- T
assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335110
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335159
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335159
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335163
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335165
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335174
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335176
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335181
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335187
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs960476028
seq_region_name: 17
source: dbSNP
start: 73335195
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335195
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335198
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335199
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335202
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335209
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062368797
seq_region_name: 17
source: dbSNP
start: 73335210
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs73343804
seq_region_name: 17
source: dbSNP
start: 73335213
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2044016315
seq_region_name: 17
source: dbSNP
start: 73335215
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599457734
seq_region_name: 17
source: dbSNP
start: 73335216
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335218
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062368893
seq_region_name: 17
source: dbSNP
start: 73335219
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1343897806
seq_region_name: 17
source: dbSNP
start: 73335220
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062368934
seq_region_name: 17
source: dbSNP
start: 73335221
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2145352765
seq_region_name: 17
source: dbSNP
start: 73335224
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335227
feature_type: variation
id: rs913549328
seq_region_name: 17
source: dbSNP
start: 73335227
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1342152568
seq_region_name: 17
source: dbSNP
start: 73335228
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2145352782
seq_region_name: 17
source: dbSNP
start: 73335233
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335234
feature_type: variation
id: rs2062368988
seq_region_name: 17
source: dbSNP
start: 73335234
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335235
feature_type: variation
id: rs2062369009
seq_region_name: 17
source: dbSNP
start: 73335235
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs945039826
seq_region_name: 17
source: dbSNP
start: 73335242
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335243
feature_type: variation
id: rs1212872681
seq_region_name: 17
source: dbSNP
start: 73335243
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335245
feature_type: variation
id: rs2062369064
seq_region_name: 17
source: dbSNP
start: 73335245
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335253
feature_type: variation
id: rs527603481
seq_region_name: 17
source: dbSNP
start: 73335253
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335255
feature_type: variation
id: rs1274015802
seq_region_name: 17
source: dbSNP
start: 73335255
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335260
feature_type: variation
id: rs925185225
seq_region_name: 17
source: dbSNP
start: 73335260
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335263
feature_type: variation
id: rs2062369136
seq_region_name: 17
source: dbSNP
start: 73335263
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335266
feature_type: variation
id: rs1414081864
seq_region_name: 17
source: dbSNP
start: 73335266
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335268
feature_type: variation
id: rs2062369161
seq_region_name: 17
source: dbSNP
start: 73335268
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335271
feature_type: variation
id: rs1225031436
seq_region_name: 17
source: dbSNP
start: 73335271
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335272
feature_type: variation
id: rs2062369206
seq_region_name: 17
source: dbSNP
start: 73335272
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335274
feature_type: variation
id: rs2062369228
seq_region_name: 17
source: dbSNP
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-
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-
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-
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73335401
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335412
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335422
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335423
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335431
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73335433
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335435
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335438
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335440
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335449
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73335451
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335454
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335455
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335459
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335460
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335463
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335464
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335466
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335467
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73335470
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335667
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335668
strand: 1
-
alleles:
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- T
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335810
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335812
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335813
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73335815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1486794783
seq_region_name: 17
source: dbSNP
start: 73335818
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335820
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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id: rs190631167
seq_region_name: 17
source: dbSNP
start: 73335831
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062373277
seq_region_name: 17
source: dbSNP
start: 73335833
strand: 1
-
alleles:
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- ACACA
assembly_name: GRCh38
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consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73335834
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335836
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335839
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335841
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335843
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73335845
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335851
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335856
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73335861
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73335864
strand: 1
-
alleles:
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- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1351947212
seq_region_name: 17
source: dbSNP
start: 73335864
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs770340664
seq_region_name: 17
source: dbSNP
start: 73335865
strand: 1
-
alleles:
- TGTGTGTG
- TGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1332012496
seq_region_name: 17
source: dbSNP
start: 73335866
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs902804279
seq_region_name: 17
source: dbSNP
start: 73335867
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1001115150
seq_region_name: 17
source: dbSNP
start: 73335871
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335873
feature_type: variation
id: rs1311758127
seq_region_name: 17
source: dbSNP
start: 73335873
strand: 1
-
alleles:
- ATGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335878
feature_type: variation
id: rs1356997135
seq_region_name: 17
source: dbSNP
start: 73335875
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1331103878
seq_region_name: 17
source: dbSNP
start: 73335876
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1381443627
seq_region_name: 17
source: dbSNP
start: 73335883
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335885
feature_type: variation
id: rs2062373641
seq_region_name: 17
source: dbSNP
start: 73335885
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335890
feature_type: variation
id: rs1032950824
seq_region_name: 17
source: dbSNP
start: 73335890
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335892
feature_type: variation
id: rs1041888018
seq_region_name: 17
source: dbSNP
start: 73335892
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335893
feature_type: variation
id: rs549260191
seq_region_name: 17
source: dbSNP
start: 73335893
strand: 1
-
alleles:
- GCACCATCCCGCATGT
- GCACCATCCCGCATGTGCACCATCCCGCATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73335916
feature_type: variation
id: rs2062373733
seq_region_name: 17
source: dbSNP
start: 73335901
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- "-"
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336024
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336048
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336061
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336062
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336063
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336064
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336074
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73336081
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336082
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336087
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336089
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336091
feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062375581
seq_region_name: 17
source: dbSNP
start: 73336095
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336105
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs755738486
seq_region_name: 17
source: dbSNP
start: 73336109
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1228887378
seq_region_name: 17
source: dbSNP
start: 73336112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062375688
seq_region_name: 17
source: dbSNP
start: 73336113
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336120
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336129
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062375746
seq_region_name: 17
source: dbSNP
start: 73336130
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs565674659
seq_region_name: 17
source: dbSNP
start: 73336137
strand: 1
-
alleles:
- GTTAAATGCTCAGCAGAGAGGGAAAGGGATGAAGTTATTTAAAAAAAAAAAAAAAAAAAAGATGAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062375782
seq_region_name: 17
source: dbSNP
start: 73336138
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1346856147
seq_region_name: 17
source: dbSNP
start: 73336144
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336146
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1799639217
seq_region_name: 17
source: dbSNP
start: 73336155
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336159
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336163
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336166
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599458693
seq_region_name: 17
source: dbSNP
start: 73336167
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1041436249
seq_region_name: 17
source: dbSNP
start: 73336170
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062375981
seq_region_name: 17
source: dbSNP
start: 73336171
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- TTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1265225581
seq_region_name: 17
source: dbSNP
start: 73336175
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1278971484
seq_region_name: 17
source: dbSNP
start: 73336177
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1159719364
seq_region_name: 17
source: dbSNP
start: 73336178
strand: 1
-
alleles:
- AAAAAAAAAAAAAAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs57845880
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1270646173
seq_region_name: 17
source: dbSNP
start: 73336179
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336185
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336186
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336187
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336189
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1489656671
seq_region_name: 17
source: dbSNP
start: 73336192
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336192
strand: 1
-
alleles:
- AAGAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336196
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336197
strand: 1
-
alleles:
- GATGA
- GA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062376485
seq_region_name: 17
source: dbSNP
start: 73336198
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336199
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336200
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336201
strand: 1
-
alleles:
- GAGAGGA
- GA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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id: rs890005846
seq_region_name: 17
source: dbSNP
start: 73336201
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336202
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062376618
seq_region_name: 17
source: dbSNP
start: 73336203
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1172553475
seq_region_name: 17
source: dbSNP
start: 73336204
strand: 1
-
alleles:
- AAAGAAAAGAAA
- AAAGAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs777613501
seq_region_name: 17
source: dbSNP
start: 73336207
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1599458784
seq_region_name: 17
source: dbSNP
start: 73336208
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1283474884
seq_region_name: 17
source: dbSNP
start: 73336210
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs902049810
seq_region_name: 17
source: dbSNP
start: 73336215
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs936157200
seq_region_name: 17
source: dbSNP
start: 73336216
strand: 1
-
alleles:
- AAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062376738
seq_region_name: 17
source: dbSNP
start: 73336216
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1599458797
seq_region_name: 17
source: dbSNP
start: 73336219
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1232859552
seq_region_name: 17
source: dbSNP
start: 73336220
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1599458804
seq_region_name: 17
source: dbSNP
start: 73336221
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336223
feature_type: variation
id: rs1599458809
seq_region_name: 17
source: dbSNP
start: 73336223
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336225
feature_type: variation
id: rs555684607
seq_region_name: 17
source: dbSNP
start: 73336225
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1315098289
seq_region_name: 17
source: dbSNP
start: 73336226
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336227
feature_type: variation
id: rs2145355129
seq_region_name: 17
source: dbSNP
start: 73336227
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336228
feature_type: variation
id: rs1164419344
seq_region_name: 17
source: dbSNP
start: 73336228
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1019702738
seq_region_name: 17
source: dbSNP
start: 73336230
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336231
feature_type: variation
id: rs889526528
seq_region_name: 17
source: dbSNP
start: 73336231
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336234
feature_type: variation
id: rs2062376965
seq_region_name: 17
source: dbSNP
start: 73336234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336236
feature_type: variation
id: rs2062376986
seq_region_name: 17
source: dbSNP
start: 73336236
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336238
feature_type: variation
id: rs372275684
seq_region_name: 17
source: dbSNP
start: 73336238
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336239
feature_type: variation
id: rs1019681126
seq_region_name: 17
source: dbSNP
start: 73336239
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336241
feature_type: variation
id: rs1362499659
seq_region_name: 17
source: dbSNP
start: 73336241
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336242
feature_type: variation
id: rs370724931
seq_region_name: 17
source: dbSNP
start: 73336242
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336244
feature_type: variation
id: rs2062377069
seq_region_name: 17
source: dbSNP
start: 73336244
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336253
feature_type: variation
id: rs2062377087
seq_region_name: 17
source: dbSNP
start: 73336253
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336254
feature_type: variation
id: rs900867180
seq_region_name: 17
source: dbSNP
start: 73336254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336261
feature_type: variation
id: rs1418132563
seq_region_name: 17
source: dbSNP
start: 73336261
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336263
feature_type: variation
id: rs374095046
seq_region_name: 17
source: dbSNP
start: 73336263
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336267
feature_type: variation
id: rs1183308037
seq_region_name: 17
source: dbSNP
start: 73336267
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336269
feature_type: variation
id: rs2145355198
seq_region_name: 17
source: dbSNP
start: 73336269
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336272
feature_type: variation
id: rs1474297606
seq_region_name: 17
source: dbSNP
start: 73336272
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336276
feature_type: variation
id: rs1025629746
seq_region_name: 17
source: dbSNP
start: 73336276
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336277
feature_type: variation
id: rs1216373158
seq_region_name: 17
source: dbSNP
start: 73336277
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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-
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336405
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336408
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73336415
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336417
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336422
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336427
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1387310131
seq_region_name: 17
source: dbSNP
start: 73336429
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336431
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1269489941
seq_region_name: 17
source: dbSNP
start: 73336432
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336435
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336436
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs560335785
seq_region_name: 17
source: dbSNP
start: 73336441
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336442
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336446
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062378965
seq_region_name: 17
source: dbSNP
start: 73336449
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336454
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336456
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336462
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336464
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336465
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73336472
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336472
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062379177
seq_region_name: 17
source: dbSNP
start: 73336478
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336486
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seq_region_name: 17
source: dbSNP
start: 73336486
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73336688
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73336701
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336707
strand: 1
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- T
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73336848
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73336849
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73336860
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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- GGGGG
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73336867
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- GGGC
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336867
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs139976784
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336876
strand: 1
-
alleles:
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- TT
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336876
strand: 1
-
alleles:
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- ACAGGGCTGGCCTTACAGGGCTGGCCTTACA
- ACAGGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGCCTTACA
- ACG
- ACGGGGCTGGCCTTACA
- TACA
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGC
- GGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGC
- GGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGCCTTACAGGGCTGGC
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336878
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GCCTTGCCTT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336889
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336893
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336894
strand: 1
-
alleles:
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- CC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336899
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336899
strand: 1
-
alleles:
- "-"
- CTT
- CTTACAGGGCTGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1555746335
seq_region_name: 17
source: dbSNP
start: 73336900
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1817668496
seq_region_name: 17
source: dbSNP
start: 73336900
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062383650
seq_region_name: 17
source: dbSNP
start: 73336901
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs775411368
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GGGG
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336904
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336906
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336912
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336913
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336914
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1220919369
seq_region_name: 17
source: dbSNP
start: 73336915
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336917
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336918
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336919
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336921
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336925
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336930
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062383996
seq_region_name: 17
source: dbSNP
start: 73336932
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336939
strand: 1
-
alleles:
- AGAAAG
- AG
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336940
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73336941
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062384103
seq_region_name: 17
source: dbSNP
start: 73336946
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336947
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2145356593
seq_region_name: 17
source: dbSNP
start: 73336948
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336949
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336950
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs187261644
seq_region_name: 17
source: dbSNP
start: 73336954
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062384227
seq_region_name: 17
source: dbSNP
start: 73336955
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1599459653
seq_region_name: 17
source: dbSNP
start: 73336958
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73336960
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1360169349
seq_region_name: 17
source: dbSNP
start: 73336961
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1273816267
seq_region_name: 17
source: dbSNP
start: 73336962
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1336695897
seq_region_name: 17
source: dbSNP
start: 73336965
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs761890483
seq_region_name: 17
source: dbSNP
start: 73336967
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs929702354
seq_region_name: 17
source: dbSNP
start: 73336969
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs767645622
seq_region_name: 17
source: dbSNP
start: 73336970
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336978
feature_type: variation
id: rs2062384399
seq_region_name: 17
source: dbSNP
start: 73336978
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336980
feature_type: variation
id: rs2062384417
seq_region_name: 17
source: dbSNP
start: 73336980
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336983
feature_type: variation
id: rs1274245713
seq_region_name: 17
source: dbSNP
start: 73336983
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336984
feature_type: variation
id: rs2062384451
seq_region_name: 17
source: dbSNP
start: 73336984
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336986
feature_type: variation
id: rs368552182
seq_region_name: 17
source: dbSNP
start: 73336986
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336987
feature_type: variation
id: rs776550262
seq_region_name: 17
source: dbSNP
start: 73336987
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336988
feature_type: variation
id: rs1024271417
seq_region_name: 17
source: dbSNP
start: 73336988
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336991
feature_type: variation
id: rs1237880419
seq_region_name: 17
source: dbSNP
start: 73336991
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73336995
feature_type: variation
id: rs2062384548
seq_region_name: 17
source: dbSNP
start: 73336995
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337003
feature_type: variation
id: rs1490446837
seq_region_name: 17
source: dbSNP
start: 73337003
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337006
feature_type: variation
id: rs2062384601
seq_region_name: 17
source: dbSNP
start: 73337006
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337008
feature_type: variation
id: rs1200812112
seq_region_name: 17
source: dbSNP
start: 73337008
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337009
feature_type: variation
id: rs2062384648
seq_region_name: 17
source: dbSNP
start: 73337009
strand: 1
-
alleles:
- G
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337009
feature_type: variation
id: rs2062384671
seq_region_name: 17
source: dbSNP
start: 73337009
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337010
feature_type: variation
id: rs1599459702
seq_region_name: 17
source: dbSNP
start: 73337010
strand: 1
-
alleles:
- TGGCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337014
feature_type: variation
id: rs2062384709
seq_region_name: 17
source: dbSNP
start: 73337010
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337013
feature_type: variation
id: rs1555746362
seq_region_name: 17
source: dbSNP
start: 73337013
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337014
feature_type: variation
id: rs1445236477
seq_region_name: 17
source: dbSNP
start: 73337014
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337020
feature_type: variation
id: rs548589952
seq_region_name: 17
source: dbSNP
start: 73337020
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337022
feature_type: variation
id: rs2062384765
seq_region_name: 17
source: dbSNP
start: 73337022
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337025
feature_type: variation
id: rs2062384797
seq_region_name: 17
source: dbSNP
start: 73337025
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337028
feature_type: variation
id: rs903139621
seq_region_name: 17
source: dbSNP
start: 73337028
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337030
feature_type: variation
id: rs1568354848
seq_region_name: 17
source: dbSNP
start: 73337029
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337030
feature_type: variation
id: rs2145356761
seq_region_name: 17
source: dbSNP
start: 73337030
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337031
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337034
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062384914
seq_region_name: 17
source: dbSNP
start: 73337037
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1331395671
seq_region_name: 17
source: dbSNP
start: 73337039
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs909516439
seq_region_name: 17
source: dbSNP
start: 73337042
strand: 1
-
alleles:
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- TGTGTGT
- TGTGTGTGT
- TGTGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs761013945
seq_region_name: 17
source: dbSNP
start: 73337042
strand: 1
-
alleles:
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- TGTGTATGTGT
- TGTGTATGTGTATGTGTATGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1555746369
seq_region_name: 17
source: dbSNP
start: 73337042
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1321883783
seq_region_name: 17
source: dbSNP
start: 73337043
strand: 1
-
alleles:
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- GTGTACGTGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337047
feature_type: variation
id: rs1244907329
seq_region_name: 17
source: dbSNP
start: 73337043
strand: 1
-
alleles:
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- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337056
feature_type: variation
id: rs1477659817
seq_region_name: 17
source: dbSNP
start: 73337044
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337046
feature_type: variation
id: rs941038941
seq_region_name: 17
source: dbSNP
start: 73337046
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1186534671
seq_region_name: 17
source: dbSNP
start: 73337046
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1105587
seq_region_name: 17
source: dbSNP
start: 73337047
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337048
feature_type: variation
id: rs538852874
seq_region_name: 17
source: dbSNP
start: 73337048
strand: 1
-
alleles:
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- T
- TGT
- TGTGTGT
- TGTGTGTGT
- TGTGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337052
feature_type: variation
id: rs1162306143
seq_region_name: 17
source: dbSNP
start: 73337048
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337049
feature_type: variation
id: rs2062385446
seq_region_name: 17
source: dbSNP
start: 73337049
strand: 1
-
alleles:
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- TGT
- TGTATGTATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337056
feature_type: variation
id: rs1167544434
seq_region_name: 17
source: dbSNP
start: 73337050
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337051
feature_type: variation
id: rs957415310
seq_region_name: 17
source: dbSNP
start: 73337051
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337054
feature_type: variation
id: rs1271394235
seq_region_name: 17
source: dbSNP
start: 73337052
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs950037576
seq_region_name: 17
source: dbSNP
start: 73337053
strand: 1
-
alleles:
- T
- TATGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337054
feature_type: variation
id: rs1555746392
seq_region_name: 17
source: dbSNP
start: 73337054
strand: 1
-
alleles:
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- TGTGTATGTGTGT
- TGTGTATGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337058
feature_type: variation
id: rs1555746393
seq_region_name: 17
source: dbSNP
start: 73337054
strand: 1
-
alleles:
- TGTGTGT
- TGTGTGTATGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337060
feature_type: variation
id: rs2062385682
seq_region_name: 17
source: dbSNP
start: 73337054
strand: 1
-
alleles:
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- TGTGTGTGT
- TGTGTGTGTGTGT
- TGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs3079765
seq_region_name: 17
source: dbSNP
start: 73337054
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1488886709
seq_region_name: 17
source: dbSNP
start: 73337055
strand: 1
-
alleles:
- TGT
- TGTATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337058
feature_type: variation
id: rs1365871641
seq_region_name: 17
source: dbSNP
start: 73337056
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337057
feature_type: variation
id: rs1406312859
seq_region_name: 17
source: dbSNP
start: 73337057
strand: 1
-
alleles:
- TGTGT
- TGTGTCTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1482913670
seq_region_name: 17
source: dbSNP
start: 73337058
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062385959
seq_region_name: 17
source: dbSNP
start: 73337059
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1017786681
seq_region_name: 17
source: dbSNP
start: 73337061
strand: 1
-
alleles:
- T
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337062
feature_type: variation
id: rs965735805
seq_region_name: 17
source: dbSNP
start: 73337062
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337063
feature_type: variation
id: rs1329793350
seq_region_name: 17
source: dbSNP
start: 73337063
strand: 1
-
alleles:
- T
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337064
feature_type: variation
id: rs1599459842
seq_region_name: 17
source: dbSNP
start: 73337064
strand: 1
-
alleles:
- G
- GCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337065
feature_type: variation
id: rs2062386091
seq_region_name: 17
source: dbSNP
start: 73337065
strand: 1
-
alleles:
- T
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337066
feature_type: variation
id: rs1436415186
seq_region_name: 17
source: dbSNP
start: 73337066
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337067
feature_type: variation
id: rs2062386143
seq_region_name: 17
source: dbSNP
start: 73337067
strand: 1
-
alleles:
- G
- GCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337067
feature_type: variation
id: rs2062386167
seq_region_name: 17
source: dbSNP
start: 73337067
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337069
feature_type: variation
id: rs2062386193
seq_region_name: 17
source: dbSNP
start: 73337069
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337073
feature_type: variation
id: rs2062386213
seq_region_name: 17
source: dbSNP
start: 73337073
strand: 1
-
alleles:
- GTG
- GTGGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337075
feature_type: variation
id: rs1270807213
seq_region_name: 17
source: dbSNP
start: 73337073
strand: 1
-
alleles:
- T
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337076
feature_type: variation
id: rs2062386252
seq_region_name: 17
source: dbSNP
start: 73337076
strand: 1
-
alleles:
- G
- GCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337081
feature_type: variation
id: rs1218128817
seq_region_name: 17
source: dbSNP
start: 73337081
strand: 1
-
alleles:
- "-"
- GA
- GTGA
- GTGTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337082
feature_type: variation
id: rs5821963
seq_region_name: 17
source: dbSNP
start: 73337083
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337085
feature_type: variation
id: rs975726221
seq_region_name: 17
source: dbSNP
start: 73337085
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337087
feature_type: variation
id: rs1367409459
seq_region_name: 17
source: dbSNP
start: 73337087
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337089
feature_type: variation
id: rs2062386379
seq_region_name: 17
source: dbSNP
start: 73337089
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337090
feature_type: variation
id: rs2062386400
seq_region_name: 17
source: dbSNP
start: 73337090
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337094
feature_type: variation
id: rs918923362
seq_region_name: 17
source: dbSNP
start: 73337094
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337096
feature_type: variation
id: rs2062386424
seq_region_name: 17
source: dbSNP
start: 73337096
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337098
feature_type: variation
id: rs1045571886
seq_region_name: 17
source: dbSNP
start: 73337098
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337106
feature_type: variation
id: rs1369674776
seq_region_name: 17
source: dbSNP
start: 73337106
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337107
feature_type: variation
id: rs930253974
seq_region_name: 17
source: dbSNP
start: 73337107
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337108
feature_type: variation
id: rs2062386521
seq_region_name: 17
source: dbSNP
start: 73337108
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337111
feature_type: variation
id: rs1431477279
seq_region_name: 17
source: dbSNP
start: 73337111
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337113
feature_type: variation
id: rs192102486
seq_region_name: 17
source: dbSNP
start: 73337113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337114
feature_type: variation
id: rs2062386595
seq_region_name: 17
source: dbSNP
start: 73337114
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337119
feature_type: variation
id: rs2062386619
seq_region_name: 17
source: dbSNP
start: 73337119
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337124
feature_type: variation
id: rs531339946
seq_region_name: 17
source: dbSNP
start: 73337124
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337125
feature_type: variation
id: rs2062386686
seq_region_name: 17
source: dbSNP
start: 73337125
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337126
feature_type: variation
id: rs941537567
seq_region_name: 17
source: dbSNP
start: 73337126
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337130
feature_type: variation
id: rs2062386740
seq_region_name: 17
source: dbSNP
start: 73337130
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337131
feature_type: variation
id: rs1033103520
seq_region_name: 17
source: dbSNP
start: 73337131
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337133
feature_type: variation
id: rs551544270
seq_region_name: 17
source: dbSNP
start: 73337133
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337134
feature_type: variation
id: rs572430968
seq_region_name: 17
source: dbSNP
start: 73337134
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337135
feature_type: variation
id: rs1484936038
seq_region_name: 17
source: dbSNP
start: 73337135
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337137
feature_type: variation
id: rs2062386829
seq_region_name: 17
source: dbSNP
start: 73337137
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337138
feature_type: variation
id: rs145755554
seq_region_name: 17
source: dbSNP
start: 73337138
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337139
feature_type: variation
id: rs2062386862
seq_region_name: 17
source: dbSNP
start: 73337139
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337139
feature_type: variation
id: rs2062386887
seq_region_name: 17
source: dbSNP
start: 73337139
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337140
feature_type: variation
id: rs2062386913
seq_region_name: 17
source: dbSNP
start: 73337140
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337142
feature_type: variation
id: rs561287617
seq_region_name: 17
source: dbSNP
start: 73337142
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337146
feature_type: variation
id: rs1255912635
seq_region_name: 17
source: dbSNP
start: 73337146
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337147
feature_type: variation
id: rs148989265
seq_region_name: 17
source: dbSNP
start: 73337147
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337148
feature_type: variation
id: rs2062387001
seq_region_name: 17
source: dbSNP
start: 73337148
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337149
feature_type: variation
id: rs1045795752
seq_region_name: 17
source: dbSNP
start: 73337149
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337150
feature_type: variation
id: rs903172088
seq_region_name: 17
source: dbSNP
start: 73337150
strand: 1
-
alleles:
- A
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73337193
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337205
strand: 1
-
alleles:
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- CCC
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73337205
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73337213
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337220
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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- CC
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337276
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337290
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337293
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73337294
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337295
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337299
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337302
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599460055
seq_region_name: 17
source: dbSNP
start: 73337306
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1396474314
seq_region_name: 17
source: dbSNP
start: 73337307
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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id: rs2062388332
seq_region_name: 17
source: dbSNP
start: 73337309
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1381260490
seq_region_name: 17
source: dbSNP
start: 73337312
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337314
feature_type: variation
id: rs1321786842
seq_region_name: 17
source: dbSNP
start: 73337314
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73337317
feature_type: variation
id: rs1391549867
seq_region_name: 17
source: dbSNP
start: 73337317
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062388422
seq_region_name: 17
source: dbSNP
start: 73337319
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs991157482
seq_region_name: 17
source: dbSNP
start: 73337330
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062388477
seq_region_name: 17
source: dbSNP
start: 73337331
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1432989118
seq_region_name: 17
source: dbSNP
start: 73337333
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337335
feature_type: variation
id: rs1296973314
seq_region_name: 17
source: dbSNP
start: 73337335
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73337339
feature_type: variation
id: rs2062388553
seq_region_name: 17
source: dbSNP
start: 73337339
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337344
feature_type: variation
id: rs2062388581
seq_region_name: 17
source: dbSNP
start: 73337344
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1025957011
seq_region_name: 17
source: dbSNP
start: 73337348
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337349
feature_type: variation
id: rs1161607763
seq_region_name: 17
source: dbSNP
start: 73337349
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337353
feature_type: variation
id: rs915586121
seq_region_name: 17
source: dbSNP
start: 73337353
strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337355
feature_type: variation
id: rs762947960
seq_region_name: 17
source: dbSNP
start: 73337353
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337359
feature_type: variation
id: rs2062388703
seq_region_name: 17
source: dbSNP
start: 73337359
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337361
feature_type: variation
id: rs1188698020
seq_region_name: 17
source: dbSNP
start: 73337361
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337363
feature_type: variation
id: rs2062388734
seq_region_name: 17
source: dbSNP
start: 73337363
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337365
feature_type: variation
id: rs950403843
seq_region_name: 17
source: dbSNP
start: 73337365
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062388785
seq_region_name: 17
source: dbSNP
start: 73337366
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337370
feature_type: variation
id: rs1260242986
seq_region_name: 17
source: dbSNP
start: 73337370
strand: 1
-
alleles:
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- GCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337382
feature_type: variation
id: rs2062388837
seq_region_name: 17
source: dbSNP
start: 73337371
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337372
feature_type: variation
id: rs2062388863
seq_region_name: 17
source: dbSNP
start: 73337372
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337377
feature_type: variation
id: rs2062388881
seq_region_name: 17
source: dbSNP
start: 73337377
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337379
feature_type: variation
id: rs532379573
seq_region_name: 17
source: dbSNP
start: 73337379
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337381
feature_type: variation
id: rs2062388934
seq_region_name: 17
source: dbSNP
start: 73337381
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337383
feature_type: variation
id: rs2062388951
seq_region_name: 17
source: dbSNP
start: 73337383
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337396
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337401
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337405
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73337410
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337413
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337417
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062389272
seq_region_name: 17
source: dbSNP
start: 73337418
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337421
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs950141880
seq_region_name: 17
source: dbSNP
start: 73337431
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337432
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1443744243
seq_region_name: 17
source: dbSNP
start: 73337437
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1008088796
seq_region_name: 17
source: dbSNP
start: 73337438
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145357866
seq_region_name: 17
source: dbSNP
start: 73337441
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337442
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337443
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062389438
seq_region_name: 17
source: dbSNP
start: 73337445
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599460204
seq_region_name: 17
source: dbSNP
start: 73337446
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337447
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1390191142
seq_region_name: 17
source: dbSNP
start: 73337449
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337452
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337454
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062389570
seq_region_name: 17
source: dbSNP
start: 73337455
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062389589
seq_region_name: 17
source: dbSNP
start: 73337458
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337468
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs867888484
seq_region_name: 17
source: dbSNP
start: 73337471
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062389648
seq_region_name: 17
source: dbSNP
start: 73337473
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1210119210
seq_region_name: 17
source: dbSNP
start: 73337475
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337476
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs997687706
seq_region_name: 17
source: dbSNP
start: 73337478
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1026524737
seq_region_name: 17
source: dbSNP
start: 73337479
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1342805323
seq_region_name: 17
source: dbSNP
start: 73337480
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062389783
seq_region_name: 17
source: dbSNP
start: 73337482
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062389799
seq_region_name: 17
source: dbSNP
start: 73337494
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062389825
seq_region_name: 17
source: dbSNP
start: 73337499
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062389846
seq_region_name: 17
source: dbSNP
start: 73337502
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062389871
seq_region_name: 17
source: dbSNP
start: 73337503
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337503
feature_type: variation
id: rs2062389889
seq_region_name: 17
source: dbSNP
start: 73337503
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337504
feature_type: variation
id: rs1054428820
seq_region_name: 17
source: dbSNP
start: 73337503
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1555746523
seq_region_name: 17
source: dbSNP
start: 73337504
strand: 1
-
alleles:
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- TGTGTGTGTGTG
- TGTGTGTGTGTGTG
- TGTGTGTGTGTGTGTG
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- TGTGTGTGTGTGTGTGTGTG
- TGTGTGTGTGTGTGTGTGTGTGTG
- TGTGTGTGTGTGTGTGTGTGTGTGTG
- TGTGTGTGTGTGTGTGTGTGTGTGTGTG
- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
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- TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337525
feature_type: variation
id: rs4035979
seq_region_name: 17
source: dbSNP
start: 73337504
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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id: rs2062390084
seq_region_name: 17
source: dbSNP
start: 73337505
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062390099
seq_region_name: 17
source: dbSNP
start: 73337505
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337507
feature_type: variation
id: rs547844561
seq_region_name: 17
source: dbSNP
start: 73337507
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1199086615
seq_region_name: 17
source: dbSNP
start: 73337509
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1414748892
seq_region_name: 17
source: dbSNP
start: 73337509
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337511
feature_type: variation
id: rs2062390191
seq_region_name: 17
source: dbSNP
start: 73337511
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337513
feature_type: variation
id: rs2062390214
seq_region_name: 17
source: dbSNP
start: 73337513
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337513
feature_type: variation
id: rs2062390232
seq_region_name: 17
source: dbSNP
start: 73337513
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337515
feature_type: variation
id: rs2062390256
seq_region_name: 17
source: dbSNP
start: 73337515
strand: 1
-
alleles:
- GTG
- GTGAGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337517
feature_type: variation
id: rs2062390275
seq_region_name: 17
source: dbSNP
start: 73337515
strand: 1
-
alleles:
- "-"
- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337515
feature_type: variation
id: rs5821964
seq_region_name: 17
source: dbSNP
start: 73337516
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337516
feature_type: variation
id: rs1006336763
seq_region_name: 17
source: dbSNP
start: 73337516
strand: 1
-
alleles:
- T
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337518
feature_type: variation
id: rs1007475570
seq_region_name: 17
source: dbSNP
start: 73337518
strand: 1
-
alleles:
- T
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337520
feature_type: variation
id: rs2062390357
seq_region_name: 17
source: dbSNP
start: 73337520
strand: 1
-
alleles:
- TGTG
- TGTGTCTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337525
feature_type: variation
id: rs1682195546
seq_region_name: 17
source: dbSNP
start: 73337522
strand: 1
-
alleles:
- T
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337524
feature_type: variation
id: rs2062390388
seq_region_name: 17
source: dbSNP
start: 73337524
strand: 1
-
alleles:
- G
- GCG
- GTGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337525
feature_type: variation
id: rs1555746540
seq_region_name: 17
source: dbSNP
start: 73337525
strand: 1
-
alleles:
- GG
- G
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337526
feature_type: variation
id: rs753740523
seq_region_name: 17
source: dbSNP
start: 73337525
strand: 1
-
alleles:
- "-"
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337525
feature_type: variation
id: rs56835252
seq_region_name: 17
source: dbSNP
start: 73337526
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337526
feature_type: variation
id: rs2062390497
seq_region_name: 17
source: dbSNP
start: 73337526
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337527
feature_type: variation
id: rs1204184247
seq_region_name: 17
source: dbSNP
start: 73337527
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337528
feature_type: variation
id: rs2062390526
seq_region_name: 17
source: dbSNP
start: 73337528
strand: 1
-
alleles:
- GAGGA
- GA
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337532
feature_type: variation
id: rs1456125294
seq_region_name: 17
source: dbSNP
start: 73337528
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337529
feature_type: variation
id: rs2062390572
seq_region_name: 17
source: dbSNP
start: 73337529
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337530
feature_type: variation
id: rs1599460332
seq_region_name: 17
source: dbSNP
start: 73337530
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337532
feature_type: variation
id: rs2062390611
seq_region_name: 17
source: dbSNP
start: 73337532
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337536
feature_type: variation
id: rs1319917460
seq_region_name: 17
source: dbSNP
start: 73337536
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337537
feature_type: variation
id: rs1599460348
seq_region_name: 17
source: dbSNP
start: 73337537
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337544
feature_type: variation
id: rs2145358228
seq_region_name: 17
source: dbSNP
start: 73337544
strand: 1
-
alleles:
- "-"
- GTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337550
feature_type: variation
id: rs2062390679
seq_region_name: 17
source: dbSNP
start: 73337551
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337552
feature_type: variation
id: rs1016872935
seq_region_name: 17
source: dbSNP
start: 73337552
strand: 1
-
alleles:
- "-"
- TAGTGTTCCATTCAGACAGTTCAGGGCAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337552
feature_type: variation
id: rs2062390725
seq_region_name: 17
source: dbSNP
start: 73337553
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73337553
feature_type: variation
id: rs780888119
seq_region_name: 17
source: dbSNP
start: 73337553
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73337717
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73337720
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337775
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337782
strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337797
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337799
strand: 1
-
alleles:
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- T
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GTTTTTTGTTTTTTGTTTTTTGTTTTT
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73337925
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337952
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337957
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337963
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337964
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337966
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337968
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337973
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337974
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs773332208
seq_region_name: 17
source: dbSNP
start: 73337981
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73337983
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337991
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1304744173
seq_region_name: 17
source: dbSNP
start: 73337992
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1025179000
seq_region_name: 17
source: dbSNP
start: 73337993
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73337994
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs906932394
seq_region_name: 17
source: dbSNP
start: 73338000
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2068731971
seq_region_name: 17
source: dbSNP
start: 73338003
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338008
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338012
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338018
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338022
feature_type: variation
id: rs1002651074
seq_region_name: 17
source: dbSNP
start: 73338022
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338024
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338024
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338026
feature_type: variation
id: rs538807338
seq_region_name: 17
source: dbSNP
start: 73338026
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338030
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338033
feature_type: variation
id: rs1599460718
seq_region_name: 17
source: dbSNP
start: 73338033
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1021955497
seq_region_name: 17
source: dbSNP
start: 73338034
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338041
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338045
feature_type: variation
id: rs1599460734
seq_region_name: 17
source: dbSNP
start: 73338045
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338047
feature_type: variation
id: rs775288479
seq_region_name: 17
source: dbSNP
start: 73338047
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338048
feature_type: variation
id: rs974963808
seq_region_name: 17
source: dbSNP
start: 73338048
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338054
feature_type: variation
id: rs563039178
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062395251
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73338071
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338074
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs974679125
seq_region_name: 17
source: dbSNP
start: 73338075
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145359405
seq_region_name: 17
source: dbSNP
start: 73338076
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1218218228
seq_region_name: 17
source: dbSNP
start: 73338084
strand: 1
-
alleles:
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- AGGAG
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062395644
seq_region_name: 17
source: dbSNP
start: 73338084
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1367873670
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338089
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs551739348
seq_region_name: 17
source: dbSNP
start: 73338091
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs1428865694
seq_region_name: 17
source: dbSNP
start: 73338092
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338095
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1463480564
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338100
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs532715919
seq_region_name: 17
source: dbSNP
start: 73338104
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338105
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062396016
seq_region_name: 17
source: dbSNP
start: 73338105
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338109
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338110
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338113
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338115
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338118
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs907487005
seq_region_name: 17
source: dbSNP
start: 73338119
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338123
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338125
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1253674991
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338129
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338130
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs184356824
seq_region_name: 17
source: dbSNP
start: 73338131
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs537472309
seq_region_name: 17
source: dbSNP
start: 73338136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338137
strand: 1
-
alleles:
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- AGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs956216884
seq_region_name: 17
source: dbSNP
start: 73338139
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062396696
seq_region_name: 17
source: dbSNP
start: 73338140
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs189298711
seq_region_name: 17
source: dbSNP
start: 73338142
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73338146
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs906709814
seq_region_name: 17
source: dbSNP
start: 73338148
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1002587416
seq_region_name: 17
source: dbSNP
start: 73338149
strand: 1
-
alleles:
- CAGTGGGTCCAG
- CAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1408438771
seq_region_name: 17
source: dbSNP
start: 73338151
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1157163559
seq_region_name: 17
source: dbSNP
start: 73338152
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs868104432
seq_region_name: 17
source: dbSNP
start: 73338153
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338154
feature_type: variation
id: rs2062396990
seq_region_name: 17
source: dbSNP
start: 73338154
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062397006
seq_region_name: 17
source: dbSNP
start: 73338156
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338158
feature_type: variation
id: rs1599460891
seq_region_name: 17
source: dbSNP
start: 73338158
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338159
feature_type: variation
id: rs2062397056
seq_region_name: 17
source: dbSNP
start: 73338159
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338164
feature_type: variation
id: rs2062397085
seq_region_name: 17
source: dbSNP
start: 73338164
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1599460892
seq_region_name: 17
source: dbSNP
start: 73338166
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062397133
seq_region_name: 17
source: dbSNP
start: 73338172
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338176
feature_type: variation
id: rs1413090240
seq_region_name: 17
source: dbSNP
start: 73338176
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062397185
seq_region_name: 17
source: dbSNP
start: 73338177
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062397207
seq_region_name: 17
source: dbSNP
start: 73338180
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338181
feature_type: variation
id: rs1599460899
seq_region_name: 17
source: dbSNP
start: 73338181
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338183
feature_type: variation
id: rs1161742062
seq_region_name: 17
source: dbSNP
start: 73338183
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338184
feature_type: variation
id: rs577137391
seq_region_name: 17
source: dbSNP
start: 73338184
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062397308
seq_region_name: 17
source: dbSNP
start: 73338187
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338188
feature_type: variation
id: rs1267323899
seq_region_name: 17
source: dbSNP
start: 73338188
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338193
feature_type: variation
id: rs764016366
seq_region_name: 17
source: dbSNP
start: 73338193
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338197
feature_type: variation
id: rs923273644
seq_region_name: 17
source: dbSNP
start: 73338197
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338199
feature_type: variation
id: rs1599460924
seq_region_name: 17
source: dbSNP
start: 73338199
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338200
feature_type: variation
id: rs1021315328
seq_region_name: 17
source: dbSNP
start: 73338200
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338204
feature_type: variation
id: rs2062397479
seq_region_name: 17
source: dbSNP
start: 73338204
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338207
feature_type: variation
id: rs1252391015
seq_region_name: 17
source: dbSNP
start: 73338207
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338212
feature_type: variation
id: rs2062397547
seq_region_name: 17
source: dbSNP
start: 73338212
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338213
feature_type: variation
id: rs1206370869
seq_region_name: 17
source: dbSNP
start: 73338213
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338216
feature_type: variation
id: rs1440401847
seq_region_name: 17
source: dbSNP
start: 73338216
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338217
feature_type: variation
id: rs2062397619
seq_region_name: 17
source: dbSNP
start: 73338217
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338223
feature_type: variation
id: rs964973499
seq_region_name: 17
source: dbSNP
start: 73338223
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338224
feature_type: variation
id: rs1362013420
seq_region_name: 17
source: dbSNP
start: 73338224
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338226
feature_type: variation
id: rs2062397708
seq_region_name: 17
source: dbSNP
start: 73338226
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338229
feature_type: variation
id: rs144610321
seq_region_name: 17
source: dbSNP
start: 73338229
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338230
feature_type: variation
id: rs112141234
seq_region_name: 17
source: dbSNP
start: 73338230
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338231
feature_type: variation
id: rs1396498689
seq_region_name: 17
source: dbSNP
start: 73338231
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338234
feature_type: variation
id: rs773071249
seq_region_name: 17
source: dbSNP
start: 73338234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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- CTCTCTC
- CTCTCTCTC
- CTCTCTCTCTCTC
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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source: dbSNP
start: 73338375
strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73338381
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73338385
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73338399
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73338403
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73338405
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73338406
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73338407
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73338408
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73338413
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73338417
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73338418
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73338421
strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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seq_region_name: 17
source: dbSNP
start: 73338421
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338424
feature_type: variation
id: rs545855258
seq_region_name: 17
source: dbSNP
start: 73338424
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338425
feature_type: variation
id: rs1210154334
seq_region_name: 17
source: dbSNP
start: 73338425
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338426
feature_type: variation
id: rs2062400061
seq_region_name: 17
source: dbSNP
start: 73338426
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs192841531
seq_region_name: 17
source: dbSNP
start: 73338429
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs780743698
seq_region_name: 17
source: dbSNP
start: 73338430
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs954660091
seq_region_name: 17
source: dbSNP
start: 73338432
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs184263040
seq_region_name: 17
source: dbSNP
start: 73338433
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062400220
seq_region_name: 17
source: dbSNP
start: 73338434
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs1454482066
seq_region_name: 17
source: dbSNP
start: 73338435
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338437
feature_type: variation
id: rs1599461281
seq_region_name: 17
source: dbSNP
start: 73338437
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
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feature_type: variation
id: rs2062400307
seq_region_name: 17
source: dbSNP
start: 73338438
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338441
feature_type: variation
id: rs547822956
seq_region_name: 17
source: dbSNP
start: 73338441
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338442
feature_type: variation
id: rs1349061791
seq_region_name: 17
source: dbSNP
start: 73338442
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338444
feature_type: variation
id: rs1392791070
seq_region_name: 17
source: dbSNP
start: 73338444
strand: 1
-
alleles:
- CCC
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338446
feature_type: variation
id: rs779547081
seq_region_name: 17
source: dbSNP
start: 73338444
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338445
feature_type: variation
id: rs1433387220
seq_region_name: 17
source: dbSNP
start: 73338445
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338447
feature_type: variation
id: rs1173576184
seq_region_name: 17
source: dbSNP
start: 73338447
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338449
feature_type: variation
id: rs2145360731
seq_region_name: 17
source: dbSNP
start: 73338449
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338451
feature_type: variation
id: rs2062400489
seq_region_name: 17
source: dbSNP
start: 73338452
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338455
feature_type: variation
id: rs1346088800
seq_region_name: 17
source: dbSNP
start: 73338455
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338457
feature_type: variation
id: rs2062400577
seq_region_name: 17
source: dbSNP
start: 73338457
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338458
feature_type: variation
id: rs1455699976
seq_region_name: 17
source: dbSNP
start: 73338458
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338460
feature_type: variation
id: rs2062400633
seq_region_name: 17
source: dbSNP
start: 73338460
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338461
feature_type: variation
id: rs2062400661
seq_region_name: 17
source: dbSNP
start: 73338461
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338471
feature_type: variation
id: rs963778490
seq_region_name: 17
source: dbSNP
start: 73338471
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338475
feature_type: variation
id: rs2062400710
seq_region_name: 17
source: dbSNP
start: 73338475
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338477
feature_type: variation
id: rs1344442511
seq_region_name: 17
source: dbSNP
start: 73338477
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338479
feature_type: variation
id: rs1199760158
seq_region_name: 17
source: dbSNP
start: 73338479
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338483
feature_type: variation
id: rs1384495372
seq_region_name: 17
source: dbSNP
start: 73338483
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338484
feature_type: variation
id: rs560080431
seq_region_name: 17
source: dbSNP
start: 73338484
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338487
feature_type: variation
id: rs2062400844
seq_region_name: 17
source: dbSNP
start: 73338487
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338489
feature_type: variation
id: rs2062400871
seq_region_name: 17
source: dbSNP
start: 73338489
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338491
feature_type: variation
id: rs749240781
seq_region_name: 17
source: dbSNP
start: 73338491
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338498
feature_type: variation
id: rs530353860
seq_region_name: 17
source: dbSNP
start: 73338498
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338500
feature_type: variation
id: rs973294324
seq_region_name: 17
source: dbSNP
start: 73338500
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338502
feature_type: variation
id: rs2062400983
seq_region_name: 17
source: dbSNP
start: 73338502
strand: 1
-
alleles:
- TTTTGTTTT
- TTTTGTTTTGTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338512
feature_type: variation
id: rs2062401008
seq_region_name: 17
source: dbSNP
start: 73338504
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338509
feature_type: variation
id: rs2062401036
seq_region_name: 17
source: dbSNP
start: 73338509
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338513
feature_type: variation
id: rs2062401061
seq_region_name: 17
source: dbSNP
start: 73338513
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338516
feature_type: variation
id: rs2062401087
seq_region_name: 17
source: dbSNP
start: 73338516
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338517
feature_type: variation
id: rs916413919
seq_region_name: 17
source: dbSNP
start: 73338517
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338520
feature_type: variation
id: rs78418467
seq_region_name: 17
source: dbSNP
start: 73338520
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338522
feature_type: variation
id: rs574823197
seq_region_name: 17
source: dbSNP
start: 73338522
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338523
feature_type: variation
id: rs969426447
seq_region_name: 17
source: dbSNP
start: 73338523
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338525
feature_type: variation
id: rs570236980
seq_region_name: 17
source: dbSNP
start: 73338525
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338527
feature_type: variation
id: rs1263952827
seq_region_name: 17
source: dbSNP
start: 73338527
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338530
feature_type: variation
id: rs542593010
seq_region_name: 17
source: dbSNP
start: 73338530
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338531
feature_type: variation
id: rs754423459
seq_region_name: 17
source: dbSNP
start: 73338531
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338532
feature_type: variation
id: rs2062401370
seq_region_name: 17
source: dbSNP
start: 73338532
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338533
feature_type: variation
id: rs1387231948
seq_region_name: 17
source: dbSNP
start: 73338533
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338535
feature_type: variation
id: rs2062401419
seq_region_name: 17
source: dbSNP
start: 73338535
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338536
feature_type: variation
id: rs1599461382
seq_region_name: 17
source: dbSNP
start: 73338536
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338538
feature_type: variation
id: rs772219309
seq_region_name: 17
source: dbSNP
start: 73338538
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338539
feature_type: variation
id: rs1368893481
seq_region_name: 17
source: dbSNP
start: 73338539
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338541
feature_type: variation
id: rs374860580
seq_region_name: 17
source: dbSNP
start: 73338541
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338542
feature_type: variation
id: rs2062401567
seq_region_name: 17
source: dbSNP
start: 73338542
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338543
feature_type: variation
id: rs1307656880
seq_region_name: 17
source: dbSNP
start: 73338543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338544
feature_type: variation
id: rs747100105
seq_region_name: 17
source: dbSNP
start: 73338544
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338545
feature_type: variation
id: rs570758406
seq_region_name: 17
source: dbSNP
start: 73338545
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338546
feature_type: variation
id: rs1259970478
seq_region_name: 17
source: dbSNP
start: 73338546
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338551
feature_type: variation
id: rs2062401694
seq_region_name: 17
source: dbSNP
start: 73338551
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338554
feature_type: variation
id: rs2062401723
seq_region_name: 17
source: dbSNP
start: 73338554
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338555
feature_type: variation
id: rs2062401751
seq_region_name: 17
source: dbSNP
start: 73338555
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338556
feature_type: variation
id: rs188895227
seq_region_name: 17
source: dbSNP
start: 73338556
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338557
feature_type: variation
id: rs915426944
seq_region_name: 17
source: dbSNP
start: 73338557
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338560
feature_type: variation
id: rs1215237524
seq_region_name: 17
source: dbSNP
start: 73338560
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338562
feature_type: variation
id: rs1012240868
seq_region_name: 17
source: dbSNP
start: 73338562
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338563
feature_type: variation
id: rs1270743590
seq_region_name: 17
source: dbSNP
start: 73338563
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338569
feature_type: variation
id: rs1250534188
seq_region_name: 17
source: dbSNP
start: 73338569
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338573
feature_type: variation
id: rs1453272383
seq_region_name: 17
source: dbSNP
start: 73338573
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338576
feature_type: variation
id: rs1191080920
seq_region_name: 17
source: dbSNP
start: 73338576
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: 3_prime_UTR_variant
end: 73338582
feature_type: variation
id: rs1409377205
seq_region_name: 17
source: dbSNP
start: 73338582
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_lost
end: 73338587
feature_type: variation
id: rs1421445023
seq_region_name: 17
source: dbSNP
start: 73338587
strand: 1
-
alleles:
- CAAACAAA
- CAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73338595
feature_type: variation
id: rs2062402026
seq_region_name: 17
source: dbSNP
start: 73338588
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338590
feature_type: variation
id: rs1157371438
seq_region_name: 17
source: dbSNP
start: 73338590
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338593
feature_type: variation
id: rs1404776637
seq_region_name: 17
source: dbSNP
start: 73338593
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338595
feature_type: variation
id: rs1363645189
seq_region_name: 17
source: dbSNP
start: 73338595
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338599
feature_type: variation
id: rs2062402196
seq_region_name: 17
source: dbSNP
start: 73338599
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338602
feature_type: variation
id: rs1176661182
seq_region_name: 17
source: dbSNP
start: 73338602
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338604
feature_type: variation
id: rs762237885
seq_region_name: 17
source: dbSNP
start: 73338604
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338606
feature_type: variation
id: rs1328183317
seq_region_name: 17
source: dbSNP
start: 73338606
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338607
feature_type: variation
id: rs553031614
seq_region_name: 17
source: dbSNP
start: 73338607
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338612
feature_type: variation
id: rs371599529
seq_region_name: 17
source: dbSNP
start: 73338612
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338613
feature_type: variation
id: rs1309222298
seq_region_name: 17
source: dbSNP
start: 73338613
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338614
feature_type: variation
id: rs763470785
seq_region_name: 17
source: dbSNP
start: 73338614
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338618
feature_type: variation
id: rs144525453
seq_region_name: 17
source: dbSNP
start: 73338618
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338620
feature_type: variation
id: rs377289427
seq_region_name: 17
source: dbSNP
start: 73338620
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338621
feature_type: variation
id: rs531489617
seq_region_name: 17
source: dbSNP
start: 73338621
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338622
feature_type: variation
id: rs1335250589
seq_region_name: 17
source: dbSNP
start: 73338622
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338624
feature_type: variation
id: rs754491697
seq_region_name: 17
source: dbSNP
start: 73338624
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338626
feature_type: variation
id: rs995789665
seq_region_name: 17
source: dbSNP
start: 73338626
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338629
feature_type: variation
id: rs1270914361
seq_region_name: 17
source: dbSNP
start: 73338629
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338633
feature_type: variation
id: rs2145361315
seq_region_name: 17
source: dbSNP
start: 73338633
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338634
feature_type: variation
id: rs1467596085
seq_region_name: 17
source: dbSNP
start: 73338634
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338639
feature_type: variation
id: rs767184830
seq_region_name: 17
source: dbSNP
start: 73338639
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338641
feature_type: variation
id: rs1234150882
seq_region_name: 17
source: dbSNP
start: 73338641
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338642
feature_type: variation
id: rs752358751
seq_region_name: 17
source: dbSNP
start: 73338642
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338644
feature_type: variation
id: rs1490244316
seq_region_name: 17
source: dbSNP
start: 73338644
strand: 1
-
alleles:
- GGGGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73338649
feature_type: variation
id: rs1176002935
seq_region_name: 17
source: dbSNP
start: 73338644
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338645
feature_type: variation
id: rs1411610848
seq_region_name: 17
source: dbSNP
start: 73338645
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338646
feature_type: variation
id: rs1475759129
seq_region_name: 17
source: dbSNP
start: 73338646
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338647
feature_type: variation
id: rs755870558
seq_region_name: 17
source: dbSNP
start: 73338647
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338648
feature_type: variation
id: rs2062402813
seq_region_name: 17
source: dbSNP
start: 73338648
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338649
feature_type: variation
id: rs777723121
seq_region_name: 17
source: dbSNP
start: 73338649
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338650
feature_type: variation
id: rs1599461580
seq_region_name: 17
source: dbSNP
start: 73338650
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73338651
feature_type: variation
id: rs147236031
seq_region_name: 17
source: dbSNP
start: 73338651
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338652
feature_type: variation
id: rs757231252
seq_region_name: 17
source: dbSNP
start: 73338652
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338657
feature_type: variation
id: rs747099510
seq_region_name: 17
source: dbSNP
start: 73338657
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338658
feature_type: variation
id: rs2145361444
seq_region_name: 17
source: dbSNP
start: 73338658
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338659
feature_type: variation
id: rs2062402944
seq_region_name: 17
source: dbSNP
start: 73338659
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338660
feature_type: variation
id: rs1439855508
seq_region_name: 17
source: dbSNP
start: 73338660
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338663
feature_type: variation
id: rs768688289
seq_region_name: 17
source: dbSNP
start: 73338663
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338668
feature_type: variation
id: rs1244745407
seq_region_name: 17
source: dbSNP
start: 73338668
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338669
feature_type: variation
id: rs1355808758
seq_region_name: 17
source: dbSNP
start: 73338669
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73338670
feature_type: variation
id: rs1004892374
seq_region_name: 17
source: dbSNP
start: 73338670
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338673
feature_type: variation
id: rs781412277
seq_region_name: 17
source: dbSNP
start: 73338673
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338675
feature_type: variation
id: rs748334451
seq_region_name: 17
source: dbSNP
start: 73338675
strand: 1
-
alleles:
- GGGGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73338680
feature_type: variation
id: rs1291258271
seq_region_name: 17
source: dbSNP
start: 73338675
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338676
feature_type: variation
id: rs770098030
seq_region_name: 17
source: dbSNP
start: 73338676
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338677
feature_type: variation
id: rs1385970637
seq_region_name: 17
source: dbSNP
start: 73338677
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338678
feature_type: variation
id: rs773595580
seq_region_name: 17
source: dbSNP
start: 73338678
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338680
feature_type: variation
id: rs1305266997
seq_region_name: 17
source: dbSNP
start: 73338680
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338681
feature_type: variation
id: rs1401041747
seq_region_name: 17
source: dbSNP
start: 73338681
strand: 1
-
alleles:
- GGGGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73338689
feature_type: variation
id: rs1202993339
seq_region_name: 17
source: dbSNP
start: 73338684
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338686
feature_type: variation
id: rs963364027
seq_region_name: 17
source: dbSNP
start: 73338686
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338687
feature_type: variation
id: rs139702398
seq_region_name: 17
source: dbSNP
start: 73338687
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338688
feature_type: variation
id: rs771401901
seq_region_name: 17
source: dbSNP
start: 73338688
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338689
feature_type: variation
id: rs1255933441
seq_region_name: 17
source: dbSNP
start: 73338689
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338690
feature_type: variation
id: rs556758068
seq_region_name: 17
source: dbSNP
start: 73338690
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338691
feature_type: variation
id: rs759080525
seq_region_name: 17
source: dbSNP
start: 73338691
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338692
feature_type: variation
id: rs2062403510
seq_region_name: 17
source: dbSNP
start: 73338692
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338696
feature_type: variation
id: rs766940174
seq_region_name: 17
source: dbSNP
start: 73338696
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338697
feature_type: variation
id: rs752334571
seq_region_name: 17
source: dbSNP
start: 73338697
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338698
feature_type: variation
id: rs145777443
seq_region_name: 17
source: dbSNP
start: 73338698
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338699
feature_type: variation
id: rs148977958
seq_region_name: 17
source: dbSNP
start: 73338699
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73338703
feature_type: variation
id: rs746494982
seq_region_name: 17
source: dbSNP
start: 73338702
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338708
feature_type: variation
id: rs201326991
seq_region_name: 17
source: dbSNP
start: 73338708
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338709
feature_type: variation
id: rs545589945
seq_region_name: 17
source: dbSNP
start: 73338709
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338714
feature_type: variation
id: rs1209710967
seq_region_name: 17
source: dbSNP
start: 73338714
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338715
feature_type: variation
id: rs2145361703
seq_region_name: 17
source: dbSNP
start: 73338715
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338718
feature_type: variation
id: rs778991229
seq_region_name: 17
source: dbSNP
start: 73338718
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338720
feature_type: variation
id: rs2062404044
seq_region_name: 17
source: dbSNP
start: 73338720
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338721
feature_type: variation
id: rs750337020
seq_region_name: 17
source: dbSNP
start: 73338721
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338723
feature_type: variation
id: rs144452885
seq_region_name: 17
source: dbSNP
start: 73338723
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338724
feature_type: variation
id: rs781156628
seq_region_name: 17
source: dbSNP
start: 73338724
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338725
feature_type: variation
id: rs748358187
seq_region_name: 17
source: dbSNP
start: 73338725
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338728
feature_type: variation
id: rs769970592
seq_region_name: 17
source: dbSNP
start: 73338728
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338729
feature_type: variation
id: rs2062404274
seq_region_name: 17
source: dbSNP
start: 73338729
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338730
feature_type: variation
id: rs778014782
seq_region_name: 17
source: dbSNP
start: 73338730
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73338734
feature_type: variation
id: rs982092760
seq_region_name: 17
source: dbSNP
start: 73338734
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338735
feature_type: variation
id: rs749636403
seq_region_name: 17
source: dbSNP
start: 73338735
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338738
feature_type: variation
id: rs1431039767
seq_region_name: 17
source: dbSNP
start: 73338738
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338740
feature_type: variation
id: rs1442210689
seq_region_name: 17
source: dbSNP
start: 73338740
strand: 1
-
alleles:
- GGTGCTGGTGCTG
- GGTGCTGGTGCTGGTGCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_insertion
end: 73338755
feature_type: variation
id: rs1194118419
seq_region_name: 17
source: dbSNP
start: 73338743
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338744
feature_type: variation
id: rs772307394
seq_region_name: 17
source: dbSNP
start: 73338744
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338745
feature_type: variation
id: rs1599461790
seq_region_name: 17
source: dbSNP
start: 73338745
strand: 1
-
alleles:
- TGGTGCTGTTGGTG
- TGGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73338761
feature_type: variation
id: rs757867307
seq_region_name: 17
source: dbSNP
start: 73338748
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338750
feature_type: variation
id: rs1321344784
seq_region_name: 17
source: dbSNP
start: 73338750
strand: 1
-
alleles:
- TGCTGTTG
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73338758
feature_type: variation
id: rs987865255
seq_region_name: 17
source: dbSNP
start: 73338751
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338758
feature_type: variation
id: rs2145361862
seq_region_name: 17
source: dbSNP
start: 73338758
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338759
feature_type: variation
id: rs1474575570
seq_region_name: 17
source: dbSNP
start: 73338759
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338761
feature_type: variation
id: rs914874533
seq_region_name: 17
source: dbSNP
start: 73338761
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338762
feature_type: variation
id: rs1187965780
seq_region_name: 17
source: dbSNP
start: 73338762
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338763
feature_type: variation
id: rs771351020
seq_region_name: 17
source: dbSNP
start: 73338763
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338764
feature_type: variation
id: rs774854358
seq_region_name: 17
source: dbSNP
start: 73338764
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338766
feature_type: variation
id: rs1599461827
seq_region_name: 17
source: dbSNP
start: 73338766
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338767
feature_type: variation
id: rs2062404836
seq_region_name: 17
source: dbSNP
start: 73338767
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338768
feature_type: variation
id: rs138505292
seq_region_name: 17
source: dbSNP
start: 73338768
strand: 1
-
alleles:
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- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1599461836
seq_region_name: 17
source: dbSNP
start: 73338769
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1599461842
seq_region_name: 17
source: dbSNP
start: 73338771
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs141386424
seq_region_name: 17
source: dbSNP
start: 73338780
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs774832542
seq_region_name: 17
source: dbSNP
start: 73338782
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs760313153
seq_region_name: 17
source: dbSNP
start: 73338785
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
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feature_type: variation
id: rs763825053
seq_region_name: 17
source: dbSNP
start: 73338786
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338787
feature_type: variation
id: rs2062405072
seq_region_name: 17
source: dbSNP
start: 73338787
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs199923333
seq_region_name: 17
source: dbSNP
start: 73338790
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338791
feature_type: variation
id: rs145172071
seq_region_name: 17
source: dbSNP
start: 73338791
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs758302541
seq_region_name: 17
source: dbSNP
start: 73338792
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338793
feature_type: variation
id: rs780077660
seq_region_name: 17
source: dbSNP
start: 73338793
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338795
feature_type: variation
id: rs868376559
seq_region_name: 17
source: dbSNP
start: 73338795
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338797
feature_type: variation
id: rs752695653
seq_region_name: 17
source: dbSNP
start: 73338797
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338798
feature_type: variation
id: rs202216577
seq_region_name: 17
source: dbSNP
start: 73338798
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338803
feature_type: variation
id: rs2062405303
seq_region_name: 17
source: dbSNP
start: 73338803
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338804
feature_type: variation
id: rs1245283370
seq_region_name: 17
source: dbSNP
start: 73338804
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338805
feature_type: variation
id: rs777963413
seq_region_name: 17
source: dbSNP
start: 73338805
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338806
feature_type: variation
id: rs1192882841
seq_region_name: 17
source: dbSNP
start: 73338806
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338807
feature_type: variation
id: rs2145362089
seq_region_name: 17
source: dbSNP
start: 73338807
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338811
feature_type: variation
id: rs1490628708
seq_region_name: 17
source: dbSNP
start: 73338811
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338812
feature_type: variation
id: rs2062405518
seq_region_name: 17
source: dbSNP
start: 73338812
strand: 1
-
alleles:
- CTG
- CTGCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_insertion
end: 73338814
feature_type: variation
id: rs2062405572
seq_region_name: 17
source: dbSNP
start: 73338812
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338815
feature_type: variation
id: rs148186444
seq_region_name: 17
source: dbSNP
start: 73338815
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338818
feature_type: variation
id: rs921698330
seq_region_name: 17
source: dbSNP
start: 73338818
strand: 1
-
alleles:
- CCTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73338821
feature_type: variation
id: rs1206061123
seq_region_name: 17
source: dbSNP
start: 73338818
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338819
feature_type: variation
id: rs749515894
seq_region_name: 17
source: dbSNP
start: 73338819
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338821
feature_type: variation
id: rs757559673
seq_region_name: 17
source: dbSNP
start: 73338821
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338822
feature_type: variation
id: rs530441434
seq_region_name: 17
source: dbSNP
start: 73338822
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338823
feature_type: variation
id: rs2062405810
seq_region_name: 17
source: dbSNP
start: 73338823
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338826
feature_type: variation
id: rs1203671674
seq_region_name: 17
source: dbSNP
start: 73338826
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338835
feature_type: variation
id: rs746344734
seq_region_name: 17
source: dbSNP
start: 73338835
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338840
feature_type: variation
id: rs772438235
seq_region_name: 17
source: dbSNP
start: 73338840
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73338841
feature_type: variation
id: rs2062406020
seq_region_name: 17
source: dbSNP
start: 73338841
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73338843
feature_type: variation
id: rs776124341
seq_region_name: 17
source: dbSNP
start: 73338843
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338844
feature_type: variation
id: rs746513867
seq_region_name: 17
source: dbSNP
start: 73338844
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338848
feature_type: variation
id: rs141527901
seq_region_name: 17
source: dbSNP
start: 73338848
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs201330590
seq_region_name: 17
source: dbSNP
start: 73338849
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338851
feature_type: variation
id: rs940586590
seq_region_name: 17
source: dbSNP
start: 73338851
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338852
feature_type: variation
id: rs765044745
seq_region_name: 17
source: dbSNP
start: 73338852
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338853
feature_type: variation
id: rs2062406330
seq_region_name: 17
source: dbSNP
start: 73338853
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338854
feature_type: variation
id: rs772848713
seq_region_name: 17
source: dbSNP
start: 73338854
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338855
feature_type: variation
id: rs1568355959
seq_region_name: 17
source: dbSNP
start: 73338855
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338857
feature_type: variation
id: rs1326172955
seq_region_name: 17
source: dbSNP
start: 73338857
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338858
feature_type: variation
id: rs762853350
seq_region_name: 17
source: dbSNP
start: 73338858
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338860
feature_type: variation
id: rs369723791
seq_region_name: 17
source: dbSNP
start: 73338860
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338866
feature_type: variation
id: rs751561374
seq_region_name: 17
source: dbSNP
start: 73338866
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338871
feature_type: variation
id: rs1330996945
seq_region_name: 17
source: dbSNP
start: 73338871
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338874
feature_type: variation
id: rs2062406720
seq_region_name: 17
source: dbSNP
start: 73338874
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338878
feature_type: variation
id: rs756119089
seq_region_name: 17
source: dbSNP
start: 73338878
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338880
feature_type: variation
id: rs764171975
seq_region_name: 17
source: dbSNP
start: 73338880
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338881
feature_type: variation
id: rs754008243
seq_region_name: 17
source: dbSNP
start: 73338881
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338885
feature_type: variation
id: rs757499946
seq_region_name: 17
source: dbSNP
start: 73338885
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338889
feature_type: variation
id: rs899147170
seq_region_name: 17
source: dbSNP
start: 73338889
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338891
feature_type: variation
id: rs2062406969
seq_region_name: 17
source: dbSNP
start: 73338891
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338896
feature_type: variation
id: rs1289305505
seq_region_name: 17
source: dbSNP
start: 73338896
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338902
feature_type: variation
id: rs373389417
seq_region_name: 17
source: dbSNP
start: 73338902
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338905
feature_type: variation
id: rs1470035155
seq_region_name: 17
source: dbSNP
start: 73338905
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338906
feature_type: variation
id: rs2062407160
seq_region_name: 17
source: dbSNP
start: 73338906
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338909
feature_type: variation
id: rs2062407201
seq_region_name: 17
source: dbSNP
start: 73338909
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338915
feature_type: variation
id: rs2145362501
seq_region_name: 17
source: dbSNP
start: 73338915
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338916
feature_type: variation
id: rs899113056
seq_region_name: 17
source: dbSNP
start: 73338916
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338917
feature_type: variation
id: rs376496362
seq_region_name: 17
source: dbSNP
start: 73338917
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338919
feature_type: variation
id: rs758866229
seq_region_name: 17
source: dbSNP
start: 73338919
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338920
feature_type: variation
id: rs780359547
seq_region_name: 17
source: dbSNP
start: 73338920
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338922
feature_type: variation
id: rs747535623
seq_region_name: 17
source: dbSNP
start: 73338922
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73338923
feature_type: variation
id: rs1183923509
seq_region_name: 17
source: dbSNP
start: 73338923
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73338926
feature_type: variation
id: rs2062407435
seq_region_name: 17
source: dbSNP
start: 73338926
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338927
feature_type: variation
id: rs776315996
seq_region_name: 17
source: dbSNP
start: 73338927
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338928
feature_type: variation
id: rs140123379
seq_region_name: 17
source: dbSNP
start: 73338928
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338929
feature_type: variation
id: rs769305408
seq_region_name: 17
source: dbSNP
start: 73338929
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73338930
feature_type: variation
id: rs1419542787
seq_region_name: 17
source: dbSNP
start: 73338930
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73338938
feature_type: variation
id: rs377260309
seq_region_name: 17
source: dbSNP
start: 73338938
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73338944
feature_type: variation
id: rs766197650
seq_region_name: 17
source: dbSNP
start: 73338944
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73338947
feature_type: variation
id: rs774214709
seq_region_name: 17
source: dbSNP
start: 73338947
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73338949
feature_type: variation
id: rs1271517627
seq_region_name: 17
source: dbSNP
start: 73338949
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73338952
feature_type: variation
id: rs759490511
seq_region_name: 17
source: dbSNP
start: 73338952
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73338954
feature_type: variation
id: rs1180575618
seq_region_name: 17
source: dbSNP
start: 73338954
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73338955
feature_type: variation
id: rs2145362641
seq_region_name: 17
source: dbSNP
start: 73338955
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73338958
feature_type: variation
id: rs764118740
seq_region_name: 17
source: dbSNP
start: 73338958
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73338960
feature_type: variation
id: rs2062407787
seq_region_name: 17
source: dbSNP
start: 73338960
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73338961
feature_type: variation
id: rs368858739
seq_region_name: 17
source: dbSNP
start: 73338961
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73338962
feature_type: variation
id: rs570913517
seq_region_name: 17
source: dbSNP
start: 73338962
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73338966
feature_type: variation
id: rs199639702
seq_region_name: 17
source: dbSNP
start: 73338966
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73338973
feature_type: variation
id: rs376367931
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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- "-"
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73339103
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339112
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062409331
seq_region_name: 17
source: dbSNP
start: 73339114
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs866272377
seq_region_name: 17
source: dbSNP
start: 73339116
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs575143284
seq_region_name: 17
source: dbSNP
start: 73339117
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339118
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73339121
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339132
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339135
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73339139
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs771892991
seq_region_name: 17
source: dbSNP
start: 73339140
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339143
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1003589684
seq_region_name: 17
source: dbSNP
start: 73339144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1036865713
seq_region_name: 17
source: dbSNP
start: 73339147
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062409718
seq_region_name: 17
source: dbSNP
start: 73339148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339149
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs892588108
seq_region_name: 17
source: dbSNP
start: 73339150
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1261104667
seq_region_name: 17
source: dbSNP
start: 73339156
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs547638745
seq_region_name: 17
source: dbSNP
start: 73339159
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1357184547
seq_region_name: 17
source: dbSNP
start: 73339160
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1314365555
seq_region_name: 17
source: dbSNP
start: 73339161
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062409887
seq_region_name: 17
source: dbSNP
start: 73339163
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339164
feature_type: variation
id: rs540273916
seq_region_name: 17
source: dbSNP
start: 73339164
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062409935
seq_region_name: 17
source: dbSNP
start: 73339168
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1023635371
seq_region_name: 17
source: dbSNP
start: 73339177
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339180
feature_type: variation
id: rs1385134387
seq_region_name: 17
source: dbSNP
start: 73339180
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339183
feature_type: variation
id: rs2062410025
seq_region_name: 17
source: dbSNP
start: 73339183
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339184
feature_type: variation
id: rs1293651334
seq_region_name: 17
source: dbSNP
start: 73339184
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339185
feature_type: variation
id: rs2062410069
seq_region_name: 17
source: dbSNP
start: 73339185
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339189
feature_type: variation
id: rs2062410091
seq_region_name: 17
source: dbSNP
start: 73339189
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339191
feature_type: variation
id: rs1568356137
seq_region_name: 17
source: dbSNP
start: 73339191
strand: 1
-
alleles:
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- TGATTGAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339195
feature_type: variation
id: rs1381888119
seq_region_name: 17
source: dbSNP
start: 73339192
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339193
feature_type: variation
id: rs2062410142
seq_region_name: 17
source: dbSNP
start: 73339193
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339196
feature_type: variation
id: rs2062410157
seq_region_name: 17
source: dbSNP
start: 73339196
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339197
feature_type: variation
id: rs1022739912
seq_region_name: 17
source: dbSNP
start: 73339197
strand: 1
-
alleles:
- ATCAGAAGA
- ATCAGAAGATCAGAAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339207
feature_type: variation
id: rs1427486272
seq_region_name: 17
source: dbSNP
start: 73339199
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339202
feature_type: variation
id: rs1291007419
seq_region_name: 17
source: dbSNP
start: 73339202
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339207
feature_type: variation
id: rs1244960447
seq_region_name: 17
source: dbSNP
start: 73339207
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339208
feature_type: variation
id: rs1453255180
seq_region_name: 17
source: dbSNP
start: 73339208
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339209
feature_type: variation
id: rs2145363310
seq_region_name: 17
source: dbSNP
start: 73339209
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339210
feature_type: variation
id: rs2098247671
seq_region_name: 17
source: dbSNP
start: 73339210
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339212
feature_type: variation
id: rs2062410289
seq_region_name: 17
source: dbSNP
start: 73339212
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339213
feature_type: variation
id: rs2062410315
seq_region_name: 17
source: dbSNP
start: 73339213
strand: 1
-
alleles:
- GTTTTTTTT
- GTTTTTTTTGTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1188718934
seq_region_name: 17
source: dbSNP
start: 73339213
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339214
feature_type: variation
id: rs1164833703
seq_region_name: 17
source: dbSNP
start: 73339214
strand: 1
-
alleles:
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- TTTTTTTTGTTTTTTTTT
- TTTTTTTTGTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1568356151
seq_region_name: 17
source: dbSNP
start: 73339214
strand: 1
-
alleles:
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- TTTTT
- TTTTTTT
- TTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339222
feature_type: variation
id: rs11290598
seq_region_name: 17
source: dbSNP
start: 73339214
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339215
feature_type: variation
id: rs1424696167
seq_region_name: 17
source: dbSNP
start: 73339215
strand: 1
-
alleles:
- TTTTTTT
- TTTTTTTGTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1568356167
seq_region_name: 17
source: dbSNP
start: 73339215
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339216
feature_type: variation
id: rs1599462397
seq_region_name: 17
source: dbSNP
start: 73339216
strand: 1
-
alleles:
- TTTTTT
- TTTTTTGTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1391565310
seq_region_name: 17
source: dbSNP
start: 73339216
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339217
feature_type: variation
id: rs1599462404
seq_region_name: 17
source: dbSNP
start: 73339217
strand: 1
-
alleles:
- TTTTT
- TTTTTGTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1568356172
seq_region_name: 17
source: dbSNP
start: 73339217
strand: 1
-
alleles:
- TTTTTTGTTTTT
- TTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339228
feature_type: variation
id: rs796921455
seq_region_name: 17
source: dbSNP
start: 73339217
strand: 1
-
alleles:
- TTTTTTGTTTTTGTTTTT
- TTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339234
feature_type: variation
id: rs1190501172
seq_region_name: 17
source: dbSNP
start: 73339217
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339218
feature_type: variation
id: rs1003444106
seq_region_name: 17
source: dbSNP
start: 73339218
strand: 1
-
alleles:
- TTTT
- TTTTGTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1555746992
seq_region_name: 17
source: dbSNP
start: 73339218
strand: 1
-
alleles:
- TTTTTGTTTTTGTTTTTGTTTTT
- TTTTTGTTTTT
- TTTTTGTTTTTGTTTTT
- TTTTTGTTTTTGTTTTTGTTTTTGTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339240
feature_type: variation
id: rs139684133
seq_region_name: 17
source: dbSNP
start: 73339218
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1447306112
seq_region_name: 17
source: dbSNP
start: 73339219
strand: 1
-
alleles:
- TTTTGTTTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339227
feature_type: variation
id: rs1290906460
seq_region_name: 17
source: dbSNP
start: 73339219
strand: 1
-
alleles:
- TT
- TTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1166475886
seq_region_name: 17
source: dbSNP
start: 73339220
strand: 1
-
alleles:
- TTTGTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339226
feature_type: variation
id: rs2062410920
seq_region_name: 17
source: dbSNP
start: 73339220
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs759040272
seq_region_name: 17
source: dbSNP
start: 73339221
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1361618669
seq_region_name: 17
source: dbSNP
start: 73339221
strand: 1
-
alleles:
- TTGTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339225
feature_type: variation
id: rs1568356194
seq_region_name: 17
source: dbSNP
start: 73339221
strand: 1
-
alleles:
- "-"
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339221
feature_type: variation
id: rs1406363211
seq_region_name: 17
source: dbSNP
start: 73339222
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339222
feature_type: variation
id: rs9904634
seq_region_name: 17
source: dbSNP
start: 73339222
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339224
feature_type: variation
id: rs1568356209
seq_region_name: 17
source: dbSNP
start: 73339222
strand: 1
-
alleles:
- TGTTTTTGTTTTTG
- GTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339235
feature_type: variation
id: rs66536408
seq_region_name: 17
source: dbSNP
start: 73339222
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339223
feature_type: variation
id: rs9896381
seq_region_name: 17
source: dbSNP
start: 73339223
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339223
feature_type: variation
id: rs1298077756
seq_region_name: 17
source: dbSNP
start: 73339223
strand: 1
-
alleles:
- GTTTTTG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339229
feature_type: variation
id: rs1568356219
seq_region_name: 17
source: dbSNP
start: 73339223
strand: 1
-
alleles:
- GTTTTTGTTTTTG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339235
feature_type: variation
id: rs1403473201
seq_region_name: 17
source: dbSNP
start: 73339223
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339224
feature_type: variation
id: rs1690256209
seq_region_name: 17
source: dbSNP
start: 73339224
strand: 1
-
alleles:
- TTTTT
- TTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339228
feature_type: variation
id: rs1345324501
seq_region_name: 17
source: dbSNP
start: 73339224
strand: 1
-
alleles:
- TTTTGTTTTTGTTTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339239
feature_type: variation
id: rs1392997435
seq_region_name: 17
source: dbSNP
start: 73339225
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339226
feature_type: variation
id: rs2062411349
seq_region_name: 17
source: dbSNP
start: 73339226
strand: 1
-
alleles:
- TTTGTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339232
feature_type: variation
id: rs2062411385
seq_region_name: 17
source: dbSNP
start: 73339226
strand: 1
-
alleles:
- TTTGTTTTTGTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339238
feature_type: variation
id: rs1440173134
seq_region_name: 17
source: dbSNP
start: 73339226
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339227
feature_type: variation
id: rs1568356230
seq_region_name: 17
source: dbSNP
start: 73339227
strand: 1
-
alleles:
- TTGTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339231
feature_type: variation
id: rs1321318051
seq_region_name: 17
source: dbSNP
start: 73339227
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339228
feature_type: variation
id: rs557602857
seq_region_name: 17
source: dbSNP
start: 73339228
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339230
feature_type: variation
id: rs1277004222
seq_region_name: 17
source: dbSNP
start: 73339228
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339229
feature_type: variation
id: rs9896383
seq_region_name: 17
source: dbSNP
start: 73339229
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339229
feature_type: variation
id: rs1568356251
seq_region_name: 17
source: dbSNP
start: 73339229
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339230
feature_type: variation
id: rs2062411658
seq_region_name: 17
source: dbSNP
start: 73339230
strand: 1
-
alleles:
- TTTTT
- TTTTTT
- TTTTTTT
- TTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339234
feature_type: variation
id: rs2062411701
seq_region_name: 17
source: dbSNP
start: 73339230
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339231
feature_type: variation
id: rs1165645099
seq_region_name: 17
source: dbSNP
start: 73339231
strand: 1
-
alleles:
- TTTTGTTTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339239
feature_type: variation
id: rs2062411790
seq_region_name: 17
source: dbSNP
start: 73339231
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339232
feature_type: variation
id: rs539923684
seq_region_name: 17
source: dbSNP
start: 73339232
strand: 1
-
alleles:
- TTTGTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339238
feature_type: variation
id: rs1367562738
seq_region_name: 17
source: dbSNP
start: 73339232
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339233
feature_type: variation
id: rs1172137552
seq_region_name: 17
source: dbSNP
start: 73339233
strand: 1
-
alleles:
- TTGTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339237
feature_type: variation
id: rs747107900
seq_region_name: 17
source: dbSNP
start: 73339233
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339234
feature_type: variation
id: rs2062411920
seq_region_name: 17
source: dbSNP
start: 73339234
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339236
feature_type: variation
id: rs1269872121
seq_region_name: 17
source: dbSNP
start: 73339234
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339235
feature_type: variation
id: rs9896390
seq_region_name: 17
source: dbSNP
start: 73339235
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339235
feature_type: variation
id: rs1356765554
seq_region_name: 17
source: dbSNP
start: 73339235
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339236
feature_type: variation
id: rs1229883241
seq_region_name: 17
source: dbSNP
start: 73339236
strand: 1
-
alleles:
- TTTTTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339247
feature_type: variation
id: rs368507991
seq_region_name: 17
source: dbSNP
start: 73339236
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339237
feature_type: variation
id: rs1253265541
seq_region_name: 17
source: dbSNP
start: 73339237
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339237
feature_type: variation
id: rs1287641316
seq_region_name: 17
source: dbSNP
start: 73339238
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339238
feature_type: variation
id: rs1221931244
seq_region_name: 17
source: dbSNP
start: 73339238
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339241
feature_type: variation
id: rs1009379758
seq_region_name: 17
source: dbSNP
start: 73339241
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339242
feature_type: variation
id: rs1284327476
seq_region_name: 17
source: dbSNP
start: 73339242
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339247
feature_type: variation
id: rs1225804757
seq_region_name: 17
source: dbSNP
start: 73339247
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339248
feature_type: variation
id: rs1208752612
seq_region_name: 17
source: dbSNP
start: 73339248
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339248
feature_type: variation
id: rs2062412367
seq_region_name: 17
source: dbSNP
start: 73339248
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339249
feature_type: variation
id: rs1249378080
seq_region_name: 17
source: dbSNP
start: 73339249
strand: 1
-
alleles:
- G
- A
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339280
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339282
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339283
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs11871000
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1349035060
seq_region_name: 17
source: dbSNP
start: 73339301
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339318
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339319
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339321
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339325
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs968314948
seq_region_name: 17
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start: 73339332
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339336
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1449921534
seq_region_name: 17
source: dbSNP
start: 73339339
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339340
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73339345
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73339347
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339349
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339351
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339357
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339361
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73339364
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339365
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145364049
seq_region_name: 17
source: dbSNP
start: 73339366
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339369
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339371
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339374
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339375
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339377
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs563966021
seq_region_name: 17
source: dbSNP
start: 73339379
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1470481563
seq_region_name: 17
source: dbSNP
start: 73339381
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs531050858
seq_region_name: 17
source: dbSNP
start: 73339383
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs930714729
seq_region_name: 17
source: dbSNP
start: 73339384
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1228896619
seq_region_name: 17
source: dbSNP
start: 73339385
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339386
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339387
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1269989114
seq_region_name: 17
source: dbSNP
start: 73339388
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1045115530
seq_region_name: 17
source: dbSNP
start: 73339389
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339391
feature_type: variation
id: rs1599462746
seq_region_name: 17
source: dbSNP
start: 73339391
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599462750
seq_region_name: 17
source: dbSNP
start: 73339393
strand: 1
-
alleles:
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- TTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339400
feature_type: variation
id: rs1204107676
seq_region_name: 17
source: dbSNP
start: 73339394
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs905183930
seq_region_name: 17
source: dbSNP
start: 73339395
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339400
feature_type: variation
id: rs1028423139
seq_region_name: 17
source: dbSNP
start: 73339400
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73339401
feature_type: variation
id: rs2062414169
seq_region_name: 17
source: dbSNP
start: 73339401
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339402
feature_type: variation
id: rs955538680
seq_region_name: 17
source: dbSNP
start: 73339402
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339405
feature_type: variation
id: rs2062414220
seq_region_name: 17
source: dbSNP
start: 73339405
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339408
feature_type: variation
id: rs987145061
seq_region_name: 17
source: dbSNP
start: 73339408
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339418
feature_type: variation
id: rs1290299775
seq_region_name: 17
source: dbSNP
start: 73339418
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339420
feature_type: variation
id: rs182229959
seq_region_name: 17
source: dbSNP
start: 73339420
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339421
feature_type: variation
id: rs2062414298
seq_region_name: 17
source: dbSNP
start: 73339421
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339422
feature_type: variation
id: rs911642072
seq_region_name: 17
source: dbSNP
start: 73339422
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339423
feature_type: variation
id: rs2062414325
seq_region_name: 17
source: dbSNP
start: 73339423
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339437
feature_type: variation
id: rs1315247530
seq_region_name: 17
source: dbSNP
start: 73339437
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339438
feature_type: variation
id: rs1599462780
seq_region_name: 17
source: dbSNP
start: 73339438
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339441
feature_type: variation
id: rs564449534
seq_region_name: 17
source: dbSNP
start: 73339441
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339442
feature_type: variation
id: rs528606091
seq_region_name: 17
source: dbSNP
start: 73339442
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339451
feature_type: variation
id: rs1401145127
seq_region_name: 17
source: dbSNP
start: 73339451
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339456
feature_type: variation
id: rs971745532
seq_region_name: 17
source: dbSNP
start: 73339456
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339458
feature_type: variation
id: rs2062414513
seq_region_name: 17
source: dbSNP
start: 73339458
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339464
feature_type: variation
id: rs1475108941
seq_region_name: 17
source: dbSNP
start: 73339464
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339466
feature_type: variation
id: rs2062414564
seq_region_name: 17
source: dbSNP
start: 73339466
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339467
feature_type: variation
id: rs2145364294
seq_region_name: 17
source: dbSNP
start: 73339467
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339468
feature_type: variation
id: rs1183504966
seq_region_name: 17
source: dbSNP
start: 73339468
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339469
feature_type: variation
id: rs550142248
seq_region_name: 17
source: dbSNP
start: 73339469
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73339514
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339526
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339528
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339530
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73339548
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339556
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339557
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339560
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs997068666
seq_region_name: 17
source: dbSNP
start: 73339562
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339563
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339566
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339567
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339569
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339575
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339578
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339579
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339582
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2145364651
seq_region_name: 17
source: dbSNP
start: 73339586
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062416431
seq_region_name: 17
source: dbSNP
start: 73339590
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339592
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1281157675
seq_region_name: 17
source: dbSNP
start: 73339593
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339594
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568356481
seq_region_name: 17
source: dbSNP
start: 73339595
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs569117705
seq_region_name: 17
source: dbSNP
start: 73339596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339604
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1806968673
seq_region_name: 17
source: dbSNP
start: 73339606
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568356482
seq_region_name: 17
source: dbSNP
start: 73339610
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1346063730
seq_region_name: 17
source: dbSNP
start: 73339612
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339614
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062416841
seq_region_name: 17
source: dbSNP
start: 73339616
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599462988
seq_region_name: 17
source: dbSNP
start: 73339618
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339619
feature_type: variation
id: rs1008334353
seq_region_name: 17
source: dbSNP
start: 73339619
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339623
feature_type: variation
id: rs1599462997
seq_region_name: 17
source: dbSNP
start: 73339623
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339624
feature_type: variation
id: rs1599462999
seq_region_name: 17
source: dbSNP
start: 73339624
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339627
feature_type: variation
id: rs1440082827
seq_region_name: 17
source: dbSNP
start: 73339627
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339628
feature_type: variation
id: rs2145364766
seq_region_name: 17
source: dbSNP
start: 73339628
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339633
feature_type: variation
id: rs1329737875
seq_region_name: 17
source: dbSNP
start: 73339633
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339634
feature_type: variation
id: rs1171990894
seq_region_name: 17
source: dbSNP
start: 73339634
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339635
feature_type: variation
id: rs1467379877
seq_region_name: 17
source: dbSNP
start: 73339635
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1427539166
seq_region_name: 17
source: dbSNP
start: 73339636
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339640
feature_type: variation
id: rs1599463016
seq_region_name: 17
source: dbSNP
start: 73339640
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339641
feature_type: variation
id: rs2062417149
seq_region_name: 17
source: dbSNP
start: 73339641
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339642
feature_type: variation
id: rs2062417182
seq_region_name: 17
source: dbSNP
start: 73339642
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339653
feature_type: variation
id: rs1176159818
seq_region_name: 17
source: dbSNP
start: 73339653
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339659
feature_type: variation
id: rs1599463029
seq_region_name: 17
source: dbSNP
start: 73339659
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339660
feature_type: variation
id: rs1008313910
seq_region_name: 17
source: dbSNP
start: 73339660
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1394186001
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339780
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1044200767
seq_region_name: 17
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start: 73339784
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339785
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339788
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339791
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs903816365
seq_region_name: 17
source: dbSNP
start: 73339800
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs565860670
seq_region_name: 17
source: dbSNP
start: 73339805
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73339807
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73339811
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seq_region_name: 17
source: dbSNP
start: 73339811
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs555457704
seq_region_name: 17
source: dbSNP
start: 73339812
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062419157
seq_region_name: 17
source: dbSNP
start: 73339813
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73339814
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062419214
seq_region_name: 17
source: dbSNP
start: 73339816
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339823
feature_type: variation
id: rs573723611
seq_region_name: 17
source: dbSNP
start: 73339823
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1441044501
seq_region_name: 17
source: dbSNP
start: 73339825
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062419310
seq_region_name: 17
source: dbSNP
start: 73339832
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339833
feature_type: variation
id: rs2062419360
seq_region_name: 17
source: dbSNP
start: 73339833
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339836
feature_type: variation
id: rs980897819
seq_region_name: 17
source: dbSNP
start: 73339836
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339837
feature_type: variation
id: rs186025315
seq_region_name: 17
source: dbSNP
start: 73339837
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1257541684
seq_region_name: 17
source: dbSNP
start: 73339838
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145365169
seq_region_name: 17
source: dbSNP
start: 73339839
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339846
feature_type: variation
id: rs1213482471
seq_region_name: 17
source: dbSNP
start: 73339846
strand: 1
-
alleles:
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- TTACCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339858
feature_type: variation
id: rs926703066
seq_region_name: 17
source: dbSNP
start: 73339847
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339850
feature_type: variation
id: rs2062419574
seq_region_name: 17
source: dbSNP
start: 73339850
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339854
feature_type: variation
id: rs2062419595
seq_region_name: 17
source: dbSNP
start: 73339854
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339855
feature_type: variation
id: rs2062419618
seq_region_name: 17
source: dbSNP
start: 73339855
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339860
feature_type: variation
id: rs1286708422
seq_region_name: 17
source: dbSNP
start: 73339860
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs71380173
seq_region_name: 17
source: dbSNP
start: 73339861
strand: 1
-
alleles:
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- TTTCTTTCTTT
- TTTCTTTCTTTCTTTCTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339881
feature_type: variation
id: rs939409983
seq_region_name: 17
source: dbSNP
start: 73339867
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339870
feature_type: variation
id: rs2062419741
seq_region_name: 17
source: dbSNP
start: 73339870
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339873
feature_type: variation
id: rs2062419765
seq_region_name: 17
source: dbSNP
start: 73339873
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339875
feature_type: variation
id: rs913885801
seq_region_name: 17
source: dbSNP
start: 73339873
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339878
feature_type: variation
id: rs2062419810
seq_region_name: 17
source: dbSNP
start: 73339878
strand: 1
-
alleles:
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- TTTTTTTTT
- TTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339888
feature_type: variation
id: rs367740130
seq_region_name: 17
source: dbSNP
start: 73339879
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339879
feature_type: variation
id: rs1599463175
seq_region_name: 17
source: dbSNP
start: 73339880
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339881
feature_type: variation
id: rs1453394324
seq_region_name: 17
source: dbSNP
start: 73339881
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339882
feature_type: variation
id: rs1049742457
seq_region_name: 17
source: dbSNP
start: 73339882
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339887
feature_type: variation
id: rs1346275592
seq_region_name: 17
source: dbSNP
start: 73339887
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339889
feature_type: variation
id: rs2062419983
seq_region_name: 17
source: dbSNP
start: 73339889
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339893
feature_type: variation
id: rs190846468
seq_region_name: 17
source: dbSNP
start: 73339893
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339894
feature_type: variation
id: rs1394643879
seq_region_name: 17
source: dbSNP
start: 73339894
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339896
feature_type: variation
id: rs2145365294
seq_region_name: 17
source: dbSNP
start: 73339896
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73339897
feature_type: variation
id: rs1450346359
seq_region_name: 17
source: dbSNP
start: 73339897
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
- TAGTAGAGATGGGGTTTCACCATGTTGGCCA
- "-"
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73340086
strand: 1
-
alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
- C
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73340097
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340099
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340101
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340103
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340110
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340181
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340186
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73340200
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73340202
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340203
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340206
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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feature_type: variation
id: rs932768438
seq_region_name: 17
source: dbSNP
start: 73340207
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340208
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1275923468
seq_region_name: 17
source: dbSNP
start: 73340209
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs113754588
seq_region_name: 17
source: dbSNP
start: 73340213
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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id: rs1304216548
seq_region_name: 17
source: dbSNP
start: 73340217
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1049574906
seq_region_name: 17
source: dbSNP
start: 73340218
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340222
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1400535117
seq_region_name: 17
source: dbSNP
start: 73340224
strand: 1
-
alleles:
- AAA
- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340224
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340225
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73340227
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340227
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs891147448
seq_region_name: 17
source: dbSNP
start: 73340234
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340237
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062423246
seq_region_name: 17
source: dbSNP
start: 73340238
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs890948110
seq_region_name: 17
source: dbSNP
start: 73340240
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1467992990
seq_region_name: 17
source: dbSNP
start: 73340241
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1337532069
seq_region_name: 17
source: dbSNP
start: 73340244
strand: 1
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alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340251
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs866912952
seq_region_name: 17
source: dbSNP
start: 73340252
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1467531608
seq_region_name: 17
source: dbSNP
start: 73340254
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs779202970
seq_region_name: 17
source: dbSNP
start: 73340255
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062423438
seq_region_name: 17
source: dbSNP
start: 73340258
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1362048063
seq_region_name: 17
source: dbSNP
start: 73340260
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062423482
seq_region_name: 17
source: dbSNP
start: 73340261
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1273164912
seq_region_name: 17
source: dbSNP
start: 73340262
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340263
feature_type: variation
id: rs2062423521
seq_region_name: 17
source: dbSNP
start: 73340263
strand: 1
-
alleles:
- ACCACCAC
- ACCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1329920266
seq_region_name: 17
source: dbSNP
start: 73340268
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062423567
seq_region_name: 17
source: dbSNP
start: 73340269
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062423590
seq_region_name: 17
source: dbSNP
start: 73340270
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340275
feature_type: variation
id: rs2062423609
seq_region_name: 17
source: dbSNP
start: 73340275
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062423637
seq_region_name: 17
source: dbSNP
start: 73340279
strand: 1
-
alleles:
- A
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340280
feature_type: variation
id: rs551347734
seq_region_name: 17
source: dbSNP
start: 73340280
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340286
feature_type: variation
id: rs1599463479
seq_region_name: 17
source: dbSNP
start: 73340286
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340292
feature_type: variation
id: rs1240212775
seq_region_name: 17
source: dbSNP
start: 73340292
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340294
feature_type: variation
id: rs943841840
seq_region_name: 17
source: dbSNP
start: 73340294
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340296
feature_type: variation
id: rs2062423774
seq_region_name: 17
source: dbSNP
start: 73340296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340303
feature_type: variation
id: rs1037253588
seq_region_name: 17
source: dbSNP
start: 73340303
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340305
feature_type: variation
id: rs561296655
seq_region_name: 17
source: dbSNP
start: 73340305
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340307
feature_type: variation
id: rs2062423850
seq_region_name: 17
source: dbSNP
start: 73340307
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340309
feature_type: variation
id: rs2062423874
seq_region_name: 17
source: dbSNP
start: 73340309
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340311
feature_type: variation
id: rs2062423899
seq_region_name: 17
source: dbSNP
start: 73340311
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340317
feature_type: variation
id: rs1599463497
seq_region_name: 17
source: dbSNP
start: 73340317
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340321
feature_type: variation
id: rs1279802377
seq_region_name: 17
source: dbSNP
start: 73340321
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340325
feature_type: variation
id: rs2062423959
seq_region_name: 17
source: dbSNP
start: 73340325
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340329
feature_type: variation
id: rs1202613528
seq_region_name: 17
source: dbSNP
start: 73340329
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340333
feature_type: variation
id: rs2062424009
seq_region_name: 17
source: dbSNP
start: 73340333
strand: 1
-
alleles:
- GTCACTCCCTATCTCTGCCCCTACCGGTCACTCCCTAT
- GTCACTCCCTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340373
feature_type: variation
id: rs1485674795
seq_region_name: 17
source: dbSNP
start: 73340336
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340340
feature_type: variation
id: rs2062424055
seq_region_name: 17
source: dbSNP
start: 73340340
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340343
feature_type: variation
id: rs996077773
seq_region_name: 17
source: dbSNP
start: 73340343
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340345
feature_type: variation
id: rs2145366237
seq_region_name: 17
source: dbSNP
start: 73340345
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340349
feature_type: variation
id: rs2062424108
seq_region_name: 17
source: dbSNP
start: 73340349
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340352
feature_type: variation
id: rs2062424141
seq_region_name: 17
source: dbSNP
start: 73340352
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340357
feature_type: variation
id: rs1260695714
seq_region_name: 17
source: dbSNP
start: 73340357
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340360
feature_type: variation
id: rs1238764309
seq_region_name: 17
source: dbSNP
start: 73340360
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340361
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73340399
strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340415
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1033321765
seq_region_name: 17
source: dbSNP
start: 73340416
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340417
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340418
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062424659
seq_region_name: 17
source: dbSNP
start: 73340419
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340423
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062424709
seq_region_name: 17
source: dbSNP
start: 73340427
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340430
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs567351031
seq_region_name: 17
source: dbSNP
start: 73340442
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1472585356
seq_region_name: 17
source: dbSNP
start: 73340445
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs992040596
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340449
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340452
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1002438522
seq_region_name: 17
source: dbSNP
start: 73340453
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340455
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340461
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340472
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340477
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340480
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340482
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340486
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340487
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73340488
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340488
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340490
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1940210647
seq_region_name: 17
source: dbSNP
start: 73340490
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340494
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1284463963
seq_region_name: 17
source: dbSNP
start: 73340496
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs886462838
seq_region_name: 17
source: dbSNP
start: 73340499
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340502
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340507
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340507
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340509
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340509
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340514
feature_type: variation
id: rs2062425395
seq_region_name: 17
source: dbSNP
start: 73340514
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340516
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340516
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340520
feature_type: variation
id: rs2062425445
seq_region_name: 17
source: dbSNP
start: 73340520
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340521
feature_type: variation
id: rs1324502571
seq_region_name: 17
source: dbSNP
start: 73340521
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340527
feature_type: variation
id: rs2062425487
seq_region_name: 17
source: dbSNP
start: 73340522
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340525
feature_type: variation
id: rs1014147301
seq_region_name: 17
source: dbSNP
start: 73340525
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340528
feature_type: variation
id: rs2062425534
seq_region_name: 17
source: dbSNP
start: 73340528
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340533
feature_type: variation
id: rs2145366617
seq_region_name: 17
source: dbSNP
start: 73340533
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340537
feature_type: variation
id: rs2062425580
seq_region_name: 17
source: dbSNP
start: 73340537
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340540
feature_type: variation
id: rs1400556542
seq_region_name: 17
source: dbSNP
start: 73340540
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340543
feature_type: variation
id: rs2062425617
seq_region_name: 17
source: dbSNP
start: 73340543
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340545
feature_type: variation
id: rs2062425650
seq_region_name: 17
source: dbSNP
start: 73340545
strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340551
feature_type: variation
id: rs2062425676
seq_region_name: 17
source: dbSNP
start: 73340547
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340548
feature_type: variation
id: rs1351650680
seq_region_name: 17
source: dbSNP
start: 73340548
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340549
feature_type: variation
id: rs925154896
seq_region_name: 17
source: dbSNP
start: 73340549
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340550
feature_type: variation
id: rs55836980
seq_region_name: 17
source: dbSNP
start: 73340550
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340552
feature_type: variation
id: rs1301368920
seq_region_name: 17
source: dbSNP
start: 73340552
strand: 1
-
alleles:
- CTTTACTTT
- CTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340561
feature_type: variation
id: rs2062425796
seq_region_name: 17
source: dbSNP
start: 73340553
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340554
feature_type: variation
id: rs2062425829
seq_region_name: 17
source: dbSNP
start: 73340554
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340566
feature_type: variation
id: rs753093350
seq_region_name: 17
source: dbSNP
start: 73340566
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340568
feature_type: variation
id: rs1225485276
seq_region_name: 17
source: dbSNP
start: 73340568
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340575
feature_type: variation
id: rs1414773992
seq_region_name: 17
source: dbSNP
start: 73340575
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340581
feature_type: variation
id: rs1165245613
seq_region_name: 17
source: dbSNP
start: 73340581
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340586
feature_type: variation
id: rs2062425900
seq_region_name: 17
source: dbSNP
start: 73340586
strand: 1
-
alleles:
- AA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340588
feature_type: variation
id: rs2062425924
seq_region_name: 17
source: dbSNP
start: 73340587
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340591
feature_type: variation
id: rs2062425949
seq_region_name: 17
source: dbSNP
start: 73340591
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340594
feature_type: variation
id: rs1662649438
seq_region_name: 17
source: dbSNP
start: 73340594
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340595
feature_type: variation
id: rs1474607868
seq_region_name: 17
source: dbSNP
start: 73340595
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340599
feature_type: variation
id: rs2062425969
seq_region_name: 17
source: dbSNP
start: 73340599
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340600
feature_type: variation
id: rs967162585
seq_region_name: 17
source: dbSNP
start: 73340600
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340601
feature_type: variation
id: rs12938253
seq_region_name: 17
source: dbSNP
start: 73340601
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340607
feature_type: variation
id: rs1304991023
seq_region_name: 17
source: dbSNP
start: 73340607
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340608
feature_type: variation
id: rs2145366745
seq_region_name: 17
source: dbSNP
start: 73340608
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340609
feature_type: variation
id: rs2062426068
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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start: 73340613
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340617
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062426236
seq_region_name: 17
source: dbSNP
start: 73340624
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062426269
seq_region_name: 17
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start: 73340624
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062426302
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source: dbSNP
start: 73340627
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340630
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599463665
seq_region_name: 17
source: dbSNP
start: 73340632
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340635
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340638
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1450587064
seq_region_name: 17
source: dbSNP
start: 73340639
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340640
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145366850
seq_region_name: 17
source: dbSNP
start: 73340642
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1290082111
seq_region_name: 17
source: dbSNP
start: 73340644
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145366865
seq_region_name: 17
source: dbSNP
start: 73340645
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1229684140
seq_region_name: 17
source: dbSNP
start: 73340649
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426517
seq_region_name: 17
source: dbSNP
start: 73340650
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426533
seq_region_name: 17
source: dbSNP
start: 73340651
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426558
seq_region_name: 17
source: dbSNP
start: 73340656
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426585
seq_region_name: 17
source: dbSNP
start: 73340658
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs912530071
seq_region_name: 17
source: dbSNP
start: 73340660
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426626
seq_region_name: 17
source: dbSNP
start: 73340661
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1277323155
seq_region_name: 17
source: dbSNP
start: 73340663
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1316518620
seq_region_name: 17
source: dbSNP
start: 73340664
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426701
seq_region_name: 17
source: dbSNP
start: 73340666
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599463687
seq_region_name: 17
source: dbSNP
start: 73340679
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1219082650
seq_region_name: 17
source: dbSNP
start: 73340684
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599463697
seq_region_name: 17
source: dbSNP
start: 73340685
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs773423245
seq_region_name: 17
source: dbSNP
start: 73340686
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426815
seq_region_name: 17
source: dbSNP
start: 73340691
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs56059440
seq_region_name: 17
source: dbSNP
start: 73340692
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1435790064
seq_region_name: 17
source: dbSNP
start: 73340694
strand: 1
-
alleles:
- AACCAA
- AACCAACCAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1281357749
seq_region_name: 17
source: dbSNP
start: 73340695
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs985358682
seq_region_name: 17
source: dbSNP
start: 73340697
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs190262473
seq_region_name: 17
source: dbSNP
start: 73340702
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062426972
seq_region_name: 17
source: dbSNP
start: 73340703
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs140753332
seq_region_name: 17
source: dbSNP
start: 73340705
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599463740
seq_region_name: 17
source: dbSNP
start: 73340707
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340710
feature_type: variation
id: rs1484563998
seq_region_name: 17
source: dbSNP
start: 73340710
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1037075924
seq_region_name: 17
source: dbSNP
start: 73340714
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062427195
seq_region_name: 17
source: dbSNP
start: 73340715
strand: 1
-
alleles:
- ATGTAATGAAAACCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062427219
seq_region_name: 17
source: dbSNP
start: 73340715
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340716
feature_type: variation
id: rs1399914525
seq_region_name: 17
source: dbSNP
start: 73340716
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340717
feature_type: variation
id: rs2145367081
seq_region_name: 17
source: dbSNP
start: 73340717
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs540134501
seq_region_name: 17
source: dbSNP
start: 73340721
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599463760
seq_region_name: 17
source: dbSNP
start: 73340722
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340727
feature_type: variation
id: rs2062427308
seq_region_name: 17
source: dbSNP
start: 73340727
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340731
feature_type: variation
id: rs2062427326
seq_region_name: 17
source: dbSNP
start: 73340731
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340732
feature_type: variation
id: rs1479027694
seq_region_name: 17
source: dbSNP
start: 73340732
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340733
feature_type: variation
id: rs1191143246
seq_region_name: 17
source: dbSNP
start: 73340733
strand: 1
-
alleles:
- "-"
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- T
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- TTT
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- TTTTT
- TTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340733
feature_type: variation
id: rs1555747269
seq_region_name: 17
source: dbSNP
start: 73340734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340734
feature_type: variation
id: rs1300243757
seq_region_name: 17
source: dbSNP
start: 73340734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340737
feature_type: variation
id: rs746300195
seq_region_name: 17
source: dbSNP
start: 73340734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340735
feature_type: variation
id: rs1254041196
seq_region_name: 17
source: dbSNP
start: 73340735
strand: 1
-
alleles:
- TT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340736
feature_type: variation
id: rs2062427536
seq_region_name: 17
source: dbSNP
start: 73340735
strand: 1
-
alleles:
- TTT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340737
feature_type: variation
id: rs1477371864
seq_region_name: 17
source: dbSNP
start: 73340735
strand: 1
-
alleles:
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340760
feature_type: variation
id: rs10638504
seq_region_name: 17
source: dbSNP
start: 73340735
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340736
feature_type: variation
id: rs2062427804
seq_region_name: 17
source: dbSNP
start: 73340736
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340737
feature_type: variation
id: rs2062427826
seq_region_name: 17
source: dbSNP
start: 73340736
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340738
feature_type: variation
id: rs1471131913
seq_region_name: 17
source: dbSNP
start: 73340736
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340737
feature_type: variation
id: rs1174930666
seq_region_name: 17
source: dbSNP
start: 73340737
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340737
feature_type: variation
id: rs1209233753
seq_region_name: 17
source: dbSNP
start: 73340737
strand: 1
-
alleles:
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- TTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340738
feature_type: variation
id: rs2062427893
seq_region_name: 17
source: dbSNP
start: 73340737
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340737
feature_type: variation
id: rs1568356875
seq_region_name: 17
source: dbSNP
start: 73340738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340738
feature_type: variation
id: rs867454810
seq_region_name: 17
source: dbSNP
start: 73340738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340739
feature_type: variation
id: rs2062427962
seq_region_name: 17
source: dbSNP
start: 73340738
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340740
feature_type: variation
id: rs2062427988
seq_region_name: 17
source: dbSNP
start: 73340738
strand: 1
-
alleles:
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- TTTTCTTTT
- TTTTGTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340741
feature_type: variation
id: rs1568356877
seq_region_name: 17
source: dbSNP
start: 73340738
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340738
feature_type: variation
id: rs1280698127
seq_region_name: 17
source: dbSNP
start: 73340739
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340739
feature_type: variation
id: rs931609941
seq_region_name: 17
source: dbSNP
start: 73340739
strand: 1
-
alleles:
- TT
- TTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340740
feature_type: variation
id: rs2062428064
seq_region_name: 17
source: dbSNP
start: 73340739
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340740
feature_type: variation
id: rs1353101956
seq_region_name: 17
source: dbSNP
start: 73340740
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340742
feature_type: variation
id: rs2062428116
seq_region_name: 17
source: dbSNP
start: 73340740
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340741
feature_type: variation
id: rs1049010863
seq_region_name: 17
source: dbSNP
start: 73340741
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340743
feature_type: variation
id: rs1310207742
seq_region_name: 17
source: dbSNP
start: 73340741
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340742
feature_type: variation
id: rs2062428188
seq_region_name: 17
source: dbSNP
start: 73340742
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340744
feature_type: variation
id: rs1406567326
seq_region_name: 17
source: dbSNP
start: 73340742
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340743
feature_type: variation
id: rs1175114641
seq_region_name: 17
source: dbSNP
start: 73340743
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340744
feature_type: variation
id: rs1302635073
seq_region_name: 17
source: dbSNP
start: 73340744
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340744
feature_type: variation
id: rs1568356885
seq_region_name: 17
source: dbSNP
start: 73340745
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340745
feature_type: variation
id: rs906048039
seq_region_name: 17
source: dbSNP
start: 73340745
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340745
feature_type: variation
id: rs2062428325
seq_region_name: 17
source: dbSNP
start: 73340745
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340746
feature_type: variation
id: rs2145367427
seq_region_name: 17
source: dbSNP
start: 73340747
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340747
feature_type: variation
id: rs2062428343
seq_region_name: 17
source: dbSNP
start: 73340747
strand: 1
-
alleles:
- TT
- TTCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340749
feature_type: variation
id: rs1373314115
seq_region_name: 17
source: dbSNP
start: 73340748
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340749
feature_type: variation
id: rs2145367455
seq_region_name: 17
source: dbSNP
start: 73340749
strand: 1
-
alleles:
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- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340751
feature_type: variation
id: rs2062428417
seq_region_name: 17
source: dbSNP
start: 73340749
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340749
feature_type: variation
id: rs1433175984
seq_region_name: 17
source: dbSNP
start: 73340750
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340750
feature_type: variation
id: rs1599463931
seq_region_name: 17
source: dbSNP
start: 73340750
strand: 1
-
alleles:
- TTTTTTTTTTTGAGATGGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340768
feature_type: variation
id: rs762520218
seq_region_name: 17
source: dbSNP
start: 73340750
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340753
feature_type: variation
id: rs2062428522
seq_region_name: 17
source: dbSNP
start: 73340751
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340752
feature_type: variation
id: rs2062428545
seq_region_name: 17
source: dbSNP
start: 73340752
strand: 1
-
alleles:
- TTTTTTTTG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340761
feature_type: variation
id: rs2062428568
seq_region_name: 17
source: dbSNP
start: 73340753
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340754
feature_type: variation
id: rs55916810
seq_region_name: 17
source: dbSNP
start: 73340754
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340755
feature_type: variation
id: rs58762822
seq_region_name: 17
source: dbSNP
start: 73340755
strand: 1
-
alleles:
- TTTG
- TTTGTTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340761
feature_type: variation
id: rs2062428638
seq_region_name: 17
source: dbSNP
start: 73340758
strand: 1
-
alleles:
- TGAGATGGAGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340770
feature_type: variation
id: rs1371664253
seq_region_name: 17
source: dbSNP
start: 73340760
strand: 1
-
alleles:
- "-"
- TTTGAATTGG
- TTTTG
- TTTTTA
- TTTTTTA
- TTTTTTG
- TTTTTTGGATTGG
- TTTTTTGTTTG
- TTTTTTTATGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340760
feature_type: variation
id: rs2062428684
seq_region_name: 17
source: dbSNP
start: 73340761
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340761
feature_type: variation
id: rs866240833
seq_region_name: 17
source: dbSNP
start: 73340761
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340761
feature_type: variation
id: rs1157584541
seq_region_name: 17
source: dbSNP
start: 73340761
strand: 1
-
alleles:
- GAGA
- GA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340764
feature_type: variation
id: rs2062428791
seq_region_name: 17
source: dbSNP
start: 73340761
strand: 1
-
alleles:
- GAGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340764
feature_type: variation
id: rs2062428810
seq_region_name: 17
source: dbSNP
start: 73340761
strand: 1
-
alleles:
- GAGATGGAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340769
feature_type: variation
id: rs1325875172
seq_region_name: 17
source: dbSNP
start: 73340761
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340762
feature_type: variation
id: rs867278795
seq_region_name: 17
source: dbSNP
start: 73340762
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340763
feature_type: variation
id: rs1306528342
seq_region_name: 17
source: dbSNP
start: 73340763
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340764
feature_type: variation
id: rs1384380640
seq_region_name: 17
source: dbSNP
start: 73340764
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340767
feature_type: variation
id: rs2062428891
seq_region_name: 17
source: dbSNP
start: 73340766
strand: 1
-
alleles:
- GGAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340769
feature_type: variation
id: rs2062428909
seq_region_name: 17
source: dbSNP
start: 73340766
strand: 1
-
alleles:
- GGAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340769
feature_type: variation
id: rs2062428930
seq_region_name: 17
source: dbSNP
start: 73340766
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340767
feature_type: variation
id: rs2062428949
seq_region_name: 17
source: dbSNP
start: 73340767
strand: 1
-
alleles:
- A
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1379162011
seq_region_name: 17
source: dbSNP
start: 73340768
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340769
feature_type: variation
id: rs2062428989
seq_region_name: 17
source: dbSNP
start: 73340769
strand: 1
-
alleles:
- TTTT
- TTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340773
feature_type: variation
id: rs2062429019
seq_region_name: 17
source: dbSNP
start: 73340770
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340772
feature_type: variation
id: rs1278339212
seq_region_name: 17
source: dbSNP
start: 73340772
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340774
feature_type: variation
id: rs1372677541
seq_region_name: 17
source: dbSNP
start: 73340774
strand: 1
-
alleles:
- GC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340775
feature_type: variation
id: rs2062429090
seq_region_name: 17
source: dbSNP
start: 73340774
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340775
feature_type: variation
id: rs1435299899
seq_region_name: 17
source: dbSNP
start: 73340775
strand: 1
-
alleles:
- T
- TTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340776
feature_type: variation
id: rs1555747327
seq_region_name: 17
source: dbSNP
start: 73340776
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340777
feature_type: variation
id: rs1219953278
seq_region_name: 17
source: dbSNP
start: 73340777
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340777
feature_type: variation
id: rs2062429203
seq_region_name: 17
source: dbSNP
start: 73340777
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340778
feature_type: variation
id: rs1305813333
seq_region_name: 17
source: dbSNP
start: 73340778
strand: 1
-
alleles:
- TT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340779
feature_type: variation
id: rs2062429253
seq_region_name: 17
source: dbSNP
start: 73340778
strand: 1
-
alleles:
- GTCGTC
- GTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340785
feature_type: variation
id: rs2062429276
seq_region_name: 17
source: dbSNP
start: 73340780
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340782
feature_type: variation
id: rs1233227206
seq_region_name: 17
source: dbSNP
start: 73340782
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340783
feature_type: variation
id: rs372693985
seq_region_name: 17
source: dbSNP
start: 73340783
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340784
feature_type: variation
id: rs918378446
seq_region_name: 17
source: dbSNP
start: 73340784
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340785
feature_type: variation
id: rs931054969
seq_region_name: 17
source: dbSNP
start: 73340785
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340788
feature_type: variation
id: rs2062429410
seq_region_name: 17
source: dbSNP
start: 73340788
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340790
feature_type: variation
id: rs1214396529
seq_region_name: 17
source: dbSNP
start: 73340790
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340791
feature_type: variation
id: rs2062429459
seq_region_name: 17
source: dbSNP
start: 73340791
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340792
feature_type: variation
id: rs1048113326
seq_region_name: 17
source: dbSNP
start: 73340792
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340795
feature_type: variation
id: rs2062429508
seq_region_name: 17
source: dbSNP
start: 73340795
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340796
feature_type: variation
id: rs370260561
seq_region_name: 17
source: dbSNP
start: 73340796
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340797
feature_type: variation
id: rs2062429557
seq_region_name: 17
source: dbSNP
start: 73340797
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340798
feature_type: variation
id: rs2062429585
seq_region_name: 17
source: dbSNP
start: 73340798
strand: 1
-
alleles:
- CAGTGGCACGATCTTGGCTCACCTCAAC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340825
feature_type: variation
id: rs1286810958
seq_region_name: 17
source: dbSNP
start: 73340798
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340799
feature_type: variation
id: rs1242493280
seq_region_name: 17
source: dbSNP
start: 73340799
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340802
feature_type: variation
id: rs1320112833
seq_region_name: 17
source: dbSNP
start: 73340802
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340803
feature_type: variation
id: rs2062429677
seq_region_name: 17
source: dbSNP
start: 73340803
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340806
feature_type: variation
id: rs1202326660
seq_region_name: 17
source: dbSNP
start: 73340806
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340807
feature_type: variation
id: rs1232289670
seq_region_name: 17
source: dbSNP
start: 73340807
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340810
feature_type: variation
id: rs1229200278
seq_region_name: 17
source: dbSNP
start: 73340810
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340814
feature_type: variation
id: rs2062429762
seq_region_name: 17
source: dbSNP
start: 73340814
strand: 1
-
alleles:
- GCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340817
feature_type: variation
id: rs2062429802
seq_region_name: 17
source: dbSNP
start: 73340814
strand: 1
-
alleles:
- GCTCACCTCAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340824
feature_type: variation
id: rs2062429841
seq_region_name: 17
source: dbSNP
start: 73340814
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340815
feature_type: variation
id: rs1599464046
seq_region_name: 17
source: dbSNP
start: 73340815
strand: 1
-
alleles:
- CTCACCTCAACCTC
- CTC
- CTCACCTCAACCTCACCTCAACCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340828
feature_type: variation
id: rs56149521
seq_region_name: 17
source: dbSNP
start: 73340815
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340818
feature_type: variation
id: rs1599464057
seq_region_name: 17
source: dbSNP
start: 73340818
strand: 1
-
alleles:
- CCTCAACC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340826
feature_type: variation
id: rs2062430060
seq_region_name: 17
source: dbSNP
start: 73340819
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340820
feature_type: variation
id: rs1599464060
seq_region_name: 17
source: dbSNP
start: 73340820
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340821
feature_type: variation
id: rs1599464062
seq_region_name: 17
source: dbSNP
start: 73340821
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340825
feature_type: variation
id: rs1599464066
seq_region_name: 17
source: dbSNP
start: 73340825
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340835
feature_type: variation
id: rs1287565530
seq_region_name: 17
source: dbSNP
start: 73340835
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340836
feature_type: variation
id: rs1194961693
seq_region_name: 17
source: dbSNP
start: 73340836
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340837
feature_type: variation
id: rs144599416
seq_region_name: 17
source: dbSNP
start: 73340837
strand: 1
-
alleles:
- GGGTTCAAG
- GGGTTCAAGGGTTCAAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340845
feature_type: variation
id: rs2062430280
seq_region_name: 17
source: dbSNP
start: 73340837
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340839
feature_type: variation
id: rs561875225
seq_region_name: 17
source: dbSNP
start: 73340839
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340841
feature_type: variation
id: rs1453447717
seq_region_name: 17
source: dbSNP
start: 73340841
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340842
feature_type: variation
id: rs1298270045
seq_region_name: 17
source: dbSNP
start: 73340842
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73340846
feature_type: variation
id: rs1421031835
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73340975
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73340982
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73340987
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1341193388
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1489585387
seq_region_name: 17
source: dbSNP
start: 73340998
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs966857477
seq_region_name: 17
source: dbSNP
start: 73340999
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341011
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1214962855
seq_region_name: 17
source: dbSNP
start: 73341016
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1319057888
seq_region_name: 17
source: dbSNP
start: 73341017
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062432020
seq_region_name: 17
source: dbSNP
start: 73341022
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs4638647
seq_region_name: 17
source: dbSNP
start: 73341023
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1467675223
seq_region_name: 17
source: dbSNP
start: 73341024
strand: 1
-
alleles:
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- GC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341038
feature_type: variation
id: rs2062432113
seq_region_name: 17
source: dbSNP
start: 73341028
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341031
feature_type: variation
id: rs1599464244
seq_region_name: 17
source: dbSNP
start: 73341031
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341033
feature_type: variation
id: rs533131230
seq_region_name: 17
source: dbSNP
start: 73341033
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341034
feature_type: variation
id: rs1032360815
seq_region_name: 17
source: dbSNP
start: 73341034
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341035
feature_type: variation
id: rs4638646
seq_region_name: 17
source: dbSNP
start: 73341035
strand: 1
-
alleles:
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- TAATCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062432268
seq_region_name: 17
source: dbSNP
start: 73341041
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341041
feature_type: variation
id: rs2062432280
seq_region_name: 17
source: dbSNP
start: 73341041
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341043
feature_type: variation
id: rs1328904869
seq_region_name: 17
source: dbSNP
start: 73341043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341045
feature_type: variation
id: rs2062432322
seq_region_name: 17
source: dbSNP
start: 73341045
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341045
feature_type: variation
id: rs2062432345
seq_region_name: 17
source: dbSNP
start: 73341045
strand: 1
-
alleles:
- T
- TAT
- TATT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341046
feature_type: variation
id: rs1488526158
seq_region_name: 17
source: dbSNP
start: 73341046
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341046
feature_type: variation
id: rs1599464274
seq_region_name: 17
source: dbSNP
start: 73341046
strand: 1
-
alleles:
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- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341063
feature_type: variation
id: rs10541030
seq_region_name: 17
source: dbSNP
start: 73341046
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341046
feature_type: variation
id: rs1491259266
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341207
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341212
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062433987
seq_region_name: 17
source: dbSNP
start: 73341222
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341227
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73341228
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73341228
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73341228
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341229
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341229
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341230
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341230
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341230
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73341231
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341231
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2145369134
seq_region_name: 17
source: dbSNP
start: 73341232
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341232
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs931078351
seq_region_name: 17
source: dbSNP
start: 73341236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1488342831
seq_region_name: 17
source: dbSNP
start: 73341237
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1285863427
seq_region_name: 17
source: dbSNP
start: 73341243
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145369159
seq_region_name: 17
source: dbSNP
start: 73341247
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1271253687
seq_region_name: 17
source: dbSNP
start: 73341248
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341248
feature_type: variation
id: rs1355307302
seq_region_name: 17
source: dbSNP
start: 73341248
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341249
feature_type: variation
id: rs2062434535
seq_region_name: 17
source: dbSNP
start: 73341248
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341249
feature_type: variation
id: rs1218622128
seq_region_name: 17
source: dbSNP
start: 73341249
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1251671266
seq_region_name: 17
source: dbSNP
start: 73341249
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341250
feature_type: variation
id: rs2062434601
seq_region_name: 17
source: dbSNP
start: 73341249
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341252
feature_type: variation
id: rs2062434628
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062434661
seq_region_name: 17
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start: 73341249
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73341250
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599464500
seq_region_name: 17
source: dbSNP
start: 73341252
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062434723
seq_region_name: 17
source: dbSNP
start: 73341253
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1285840806
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1444943366
seq_region_name: 17
source: dbSNP
start: 73341258
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062434807
seq_region_name: 17
source: dbSNP
start: 73341262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062434842
seq_region_name: 17
source: dbSNP
start: 73341270
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs953890666
seq_region_name: 17
source: dbSNP
start: 73341274
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062434932
seq_region_name: 17
source: dbSNP
start: 73341278
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062434985
seq_region_name: 17
source: dbSNP
start: 73341283
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs527514005
seq_region_name: 17
source: dbSNP
start: 73341287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1400648577
seq_region_name: 17
source: dbSNP
start: 73341291
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062435078
seq_region_name: 17
source: dbSNP
start: 73341316
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1347045818
seq_region_name: 17
source: dbSNP
start: 73341320
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1191430693
seq_region_name: 17
source: dbSNP
start: 73341321
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062435160
seq_region_name: 17
source: dbSNP
start: 73341322
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1048185101
seq_region_name: 17
source: dbSNP
start: 73341323
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs927005248
seq_region_name: 17
source: dbSNP
start: 73341328
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341339
feature_type: variation
id: rs1475765882
seq_region_name: 17
source: dbSNP
start: 73341339
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062435281
seq_region_name: 17
source: dbSNP
start: 73341344
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062435308
seq_region_name: 17
source: dbSNP
start: 73341345
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1167513694
seq_region_name: 17
source: dbSNP
start: 73341351
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341353
feature_type: variation
id: rs1464433772
seq_region_name: 17
source: dbSNP
start: 73341353
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341356
feature_type: variation
id: rs2062435346
seq_region_name: 17
source: dbSNP
start: 73341356
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341358
feature_type: variation
id: rs2062435371
seq_region_name: 17
source: dbSNP
start: 73341358
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1190677604
seq_region_name: 17
source: dbSNP
start: 73341359
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062435416
seq_region_name: 17
source: dbSNP
start: 73341364
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1243358771
seq_region_name: 17
source: dbSNP
start: 73341366
strand: 1
-
alleles:
- CCCC
- CCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341369
feature_type: variation
id: rs201238572
seq_region_name: 17
source: dbSNP
start: 73341366
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1460925628
seq_region_name: 17
source: dbSNP
start: 73341369
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341370
feature_type: variation
id: rs2062435511
seq_region_name: 17
source: dbSNP
start: 73341370
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341373
feature_type: variation
id: rs2062435531
seq_region_name: 17
source: dbSNP
start: 73341373
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1056782027
seq_region_name: 17
source: dbSNP
start: 73341374
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062435590
seq_region_name: 17
source: dbSNP
start: 73341377
strand: 1
-
alleles:
- AC
- ACAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341378
feature_type: variation
id: rs1273468545
seq_region_name: 17
source: dbSNP
start: 73341377
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341379
feature_type: variation
id: rs150040470
seq_region_name: 17
source: dbSNP
start: 73341379
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341384
feature_type: variation
id: rs1387354124
seq_region_name: 17
source: dbSNP
start: 73341384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341385
feature_type: variation
id: rs2062435696
seq_region_name: 17
source: dbSNP
start: 73341385
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341387
feature_type: variation
id: rs2062435723
seq_region_name: 17
source: dbSNP
start: 73341387
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341392
feature_type: variation
id: rs1317956968
seq_region_name: 17
source: dbSNP
start: 73341392
strand: 1
-
alleles:
- CAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341394
feature_type: variation
id: rs1399208531
seq_region_name: 17
source: dbSNP
start: 73341392
strand: 1
-
alleles:
- AATGTT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341398
feature_type: variation
id: rs2062435804
seq_region_name: 17
source: dbSNP
start: 73341393
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341396
feature_type: variation
id: rs1257272753
seq_region_name: 17
source: dbSNP
start: 73341396
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341398
feature_type: variation
id: rs912644847
seq_region_name: 17
source: dbSNP
start: 73341398
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341399
feature_type: variation
id: rs965457790
seq_region_name: 17
source: dbSNP
start: 73341399
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341405
feature_type: variation
id: rs1273151918
seq_region_name: 17
source: dbSNP
start: 73341405
strand: 1
-
alleles:
- A
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341409
feature_type: variation
id: rs902695087
seq_region_name: 17
source: dbSNP
start: 73341409
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341412
feature_type: variation
id: rs1599464597
seq_region_name: 17
source: dbSNP
start: 73341412
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341419
feature_type: variation
id: rs1328197596
seq_region_name: 17
source: dbSNP
start: 73341419
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341423
feature_type: variation
id: rs2062436027
seq_region_name: 17
source: dbSNP
start: 73341423
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341425
feature_type: variation
id: rs1464351095
seq_region_name: 17
source: dbSNP
start: 73341425
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341426
feature_type: variation
id: rs575913172
seq_region_name: 17
source: dbSNP
start: 73341426
strand: 1
-
alleles:
- CCCCCCC
- CCCCCC
- CCCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341432
feature_type: variation
id: rs554784782
seq_region_name: 17
source: dbSNP
start: 73341426
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341427
feature_type: variation
id: rs182875521
seq_region_name: 17
source: dbSNP
start: 73341427
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341428
feature_type: variation
id: rs1354753521
seq_region_name: 17
source: dbSNP
start: 73341428
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341429
feature_type: variation
id: rs2062436293
seq_region_name: 17
source: dbSNP
start: 73341429
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341430
feature_type: variation
id: rs2062436314
seq_region_name: 17
source: dbSNP
start: 73341430
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341431
feature_type: variation
id: rs1228414970
seq_region_name: 17
source: dbSNP
start: 73341431
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341432
feature_type: variation
id: rs2062436361
seq_region_name: 17
source: dbSNP
start: 73341432
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341432
feature_type: variation
id: rs201143752
seq_region_name: 17
source: dbSNP
start: 73341433
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341433
feature_type: variation
id: rs1253198141
seq_region_name: 17
source: dbSNP
start: 73341433
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341433
feature_type: variation
id: rs2062436434
seq_region_name: 17
source: dbSNP
start: 73341433
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341436
feature_type: variation
id: rs1006880951
seq_region_name: 17
source: dbSNP
start: 73341436
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341439
feature_type: variation
id: rs2062436484
seq_region_name: 17
source: dbSNP
start: 73341439
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341444
feature_type: variation
id: rs931533564
seq_region_name: 17
source: dbSNP
start: 73341444
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341460
feature_type: variation
id: rs1599464640
seq_region_name: 17
source: dbSNP
start: 73341460
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341461
feature_type: variation
id: rs2062436566
seq_region_name: 17
source: dbSNP
start: 73341461
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341466
feature_type: variation
id: rs79981684
seq_region_name: 17
source: dbSNP
start: 73341466
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341468
feature_type: variation
id: rs927410214
seq_region_name: 17
source: dbSNP
start: 73341468
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341469
feature_type: variation
id: rs76405439
seq_region_name: 17
source: dbSNP
start: 73341469
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341470
feature_type: variation
id: rs973047762
seq_region_name: 17
source: dbSNP
start: 73341470
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341476
feature_type: variation
id: rs1057358237
seq_region_name: 17
source: dbSNP
start: 73341476
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341478
feature_type: variation
id: rs1213472996
seq_region_name: 17
source: dbSNP
start: 73341478
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341479
feature_type: variation
id: rs2062436767
seq_region_name: 17
source: dbSNP
start: 73341479
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341480
feature_type: variation
id: rs1276479975
seq_region_name: 17
source: dbSNP
start: 73341480
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341481
feature_type: variation
id: rs749128805
seq_region_name: 17
source: dbSNP
start: 73341481
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341486
feature_type: variation
id: rs2062436846
seq_region_name: 17
source: dbSNP
start: 73341486
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341488
feature_type: variation
id: rs1013351941
seq_region_name: 17
source: dbSNP
start: 73341488
strand: 1
-
alleles:
- CTGCAGCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341498
feature_type: variation
id: rs1599464685
seq_region_name: 17
source: dbSNP
start: 73341491
strand: 1
-
alleles:
- TGCA
- TGCATGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341495
feature_type: variation
id: rs1255955424
seq_region_name: 17
source: dbSNP
start: 73341492
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341493
feature_type: variation
id: rs2062436942
seq_region_name: 17
source: dbSNP
start: 73341493
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341494
feature_type: variation
id: rs527415208
seq_region_name: 17
source: dbSNP
start: 73341494
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341495
feature_type: variation
id: rs2062437036
seq_region_name: 17
source: dbSNP
start: 73341495
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341500
feature_type: variation
id: rs2145369819
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73341722
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73341724
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73341730
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73341731
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73341732
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341734
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73341735
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73341738
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341740
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341743
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341744
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341746
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341747
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341755
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1289023940
seq_region_name: 17
source: dbSNP
start: 73341760
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs927525676
seq_region_name: 17
source: dbSNP
start: 73341761
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73341762
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id: rs2062439076
seq_region_name: 17
source: dbSNP
start: 73341762
strand: 1
-
alleles:
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- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs750181965
seq_region_name: 17
source: dbSNP
start: 73341762
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341763
feature_type: variation
id: rs1179281329
seq_region_name: 17
source: dbSNP
start: 73341763
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341765
feature_type: variation
id: rs1019641290
seq_region_name: 17
source: dbSNP
start: 73341765
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341772
feature_type: variation
id: rs2062439173
seq_region_name: 17
source: dbSNP
start: 73341772
strand: 1
-
alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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start: 73341931
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73341947
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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start: 73341949
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73341952
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73341962
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73341963
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73341975
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73341978
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73341979
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73341980
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341981
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341987
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1306665951
seq_region_name: 17
source: dbSNP
start: 73341989
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341990
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341993
feature_type: variation
id: rs1047047579
seq_region_name: 17
source: dbSNP
start: 73341993
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73341994
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73341994
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342004
feature_type: variation
id: rs2062441262
seq_region_name: 17
source: dbSNP
start: 73342004
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342011
feature_type: variation
id: rs2062441280
seq_region_name: 17
source: dbSNP
start: 73342011
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342013
feature_type: variation
id: rs2050789867
seq_region_name: 17
source: dbSNP
start: 73342013
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342016
feature_type: variation
id: rs994624424
seq_region_name: 17
source: dbSNP
start: 73342016
strand: 1
-
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source: dbSNP
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strand: 1
-
alleles:
- CTCCTACACTCCTGCACTCCTGCCTGGAGACCACAGGATGGGAACGAGAGCTCC
- C
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- "-"
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
- CACTCCTGCACTCCTGC
- CACTCCTGC
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342064
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- GGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342073
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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id: rs1599465205
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs958547754
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342080
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062441866
seq_region_name: 17
source: dbSNP
start: 73342081
strand: 1
-
alleles:
- CCCCCC
- CCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342085
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342086
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342090
strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342090
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342093
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342095
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs958313022
seq_region_name: 17
source: dbSNP
start: 73342100
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342104
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342105
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342105
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1218536573
seq_region_name: 17
source: dbSNP
start: 73342107
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342108
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs936447806
seq_region_name: 17
source: dbSNP
start: 73342110
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1475871335
seq_region_name: 17
source: dbSNP
start: 73342112
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342115
feature_type: variation
id: rs532376154
seq_region_name: 17
source: dbSNP
start: 73342115
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342116
feature_type: variation
id: rs2062442511
seq_region_name: 17
source: dbSNP
start: 73342116
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342117
feature_type: variation
id: rs989705493
seq_region_name: 17
source: dbSNP
start: 73342117
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342123
feature_type: variation
id: rs2062442566
seq_region_name: 17
source: dbSNP
start: 73342123
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs911450744
seq_region_name: 17
source: dbSNP
start: 73342125
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062442612
seq_region_name: 17
source: dbSNP
start: 73342125
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1447180164
seq_region_name: 17
source: dbSNP
start: 73342126
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062442657
seq_region_name: 17
source: dbSNP
start: 73342127
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342130
feature_type: variation
id: rs1263465469
seq_region_name: 17
source: dbSNP
start: 73342130
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs942864746
seq_region_name: 17
source: dbSNP
start: 73342132
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342134
feature_type: variation
id: rs1041184112
seq_region_name: 17
source: dbSNP
start: 73342134
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342135
feature_type: variation
id: rs1053357266
seq_region_name: 17
source: dbSNP
start: 73342135
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342141
feature_type: variation
id: rs2062442770
seq_region_name: 17
source: dbSNP
start: 73342141
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342147
feature_type: variation
id: rs2062442796
seq_region_name: 17
source: dbSNP
start: 73342147
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342148
feature_type: variation
id: rs56328256
seq_region_name: 17
source: dbSNP
start: 73342148
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342153
feature_type: variation
id: rs1316063684
seq_region_name: 17
source: dbSNP
start: 73342153
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342156
feature_type: variation
id: rs2145371342
seq_region_name: 17
source: dbSNP
start: 73342156
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342158
feature_type: variation
id: rs768884719
seq_region_name: 17
source: dbSNP
start: 73342158
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342159
feature_type: variation
id: rs2062442884
seq_region_name: 17
source: dbSNP
start: 73342159
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342162
feature_type: variation
id: rs2062442915
seq_region_name: 17
source: dbSNP
start: 73342162
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342163
feature_type: variation
id: rs2062442933
seq_region_name: 17
source: dbSNP
start: 73342163
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342164
feature_type: variation
id: rs2062442960
seq_region_name: 17
source: dbSNP
start: 73342164
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342166
feature_type: variation
id: rs2145371386
seq_region_name: 17
source: dbSNP
start: 73342166
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342173
feature_type: variation
id: rs2062442992
seq_region_name: 17
source: dbSNP
start: 73342173
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342177
feature_type: variation
id: rs981067381
seq_region_name: 17
source: dbSNP
start: 73342177
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342178
feature_type: variation
id: rs1265023545
seq_region_name: 17
source: dbSNP
start: 73342178
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342181
feature_type: variation
id: rs2062443049
seq_region_name: 17
source: dbSNP
start: 73342181
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342183
feature_type: variation
id: rs11657561
seq_region_name: 17
source: dbSNP
start: 73342183
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342186
feature_type: variation
id: rs1486328702
seq_region_name: 17
source: dbSNP
start: 73342186
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342188
feature_type: variation
id: rs1035579622
seq_region_name: 17
source: dbSNP
start: 73342188
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342189
feature_type: variation
id: rs1431640072
seq_region_name: 17
source: dbSNP
start: 73342189
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342193
feature_type: variation
id: rs1328373651
seq_region_name: 17
source: dbSNP
start: 73342193
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342195
feature_type: variation
id: rs2062443203
seq_region_name: 17
source: dbSNP
start: 73342195
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342201
feature_type: variation
id: rs1321867805
seq_region_name: 17
source: dbSNP
start: 73342201
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342202
feature_type: variation
id: rs1047115355
seq_region_name: 17
source: dbSNP
start: 73342202
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342207
feature_type: variation
id: rs1259363107
seq_region_name: 17
source: dbSNP
start: 73342207
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342209
feature_type: variation
id: rs1599465361
seq_region_name: 17
source: dbSNP
start: 73342209
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342210
feature_type: variation
id: rs1427756654
seq_region_name: 17
source: dbSNP
start: 73342210
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342213
feature_type: variation
id: rs2062443328
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73342357
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342362
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342363
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73342375
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342378
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342383
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342384
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342390
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342393
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342396
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342397
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342399
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342405
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062445999
seq_region_name: 17
source: dbSNP
start: 73342406
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342411
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342414
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs910853030
seq_region_name: 17
source: dbSNP
start: 73342415
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342417
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1259459792
seq_region_name: 17
source: dbSNP
start: 73342418
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1484665320
seq_region_name: 17
source: dbSNP
start: 73342419
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1055798685
seq_region_name: 17
source: dbSNP
start: 73342421
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342422
feature_type: variation
id: rs1181245436
seq_region_name: 17
source: dbSNP
start: 73342422
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73342424
feature_type: variation
id: rs942362927
seq_region_name: 17
source: dbSNP
start: 73342424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73342428
feature_type: variation
id: rs140252873
seq_region_name: 17
source: dbSNP
start: 73342428
strand: 1
-
alleles:
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- TGATGATG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342432
feature_type: variation
id: rs2062446478
seq_region_name: 17
source: dbSNP
start: 73342428
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342431
feature_type: variation
id: rs2062446515
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs374933591
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs903030983
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1005607488
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342505
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342507
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342516
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342519
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342528
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342529
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342531
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599465637
seq_region_name: 17
source: dbSNP
start: 73342540
strand: 1
-
alleles:
- CCCCC
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342548
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342551
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342555
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342570
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342573
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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id: rs1225606425
seq_region_name: 17
source: dbSNP
start: 73342580
strand: 1
-
alleles:
- C
- CAGGTTC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1305057404
seq_region_name: 17
source: dbSNP
start: 73342581
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73342583
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342587
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73342590
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs866918921
seq_region_name: 17
source: dbSNP
start: 73342596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1234426928
seq_region_name: 17
source: dbSNP
start: 73342600
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs565821488
seq_region_name: 17
source: dbSNP
start: 73342601
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73342608
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1484594209
seq_region_name: 17
source: dbSNP
start: 73342609
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062448724
seq_region_name: 17
source: dbSNP
start: 73342611
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73342614
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id: rs1314214372
seq_region_name: 17
source: dbSNP
start: 73342614
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1209316132
seq_region_name: 17
source: dbSNP
start: 73342618
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1233451371
seq_region_name: 17
source: dbSNP
start: 73342620
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062448822
seq_region_name: 17
source: dbSNP
start: 73342621
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342622
feature_type: variation
id: rs1289115848
seq_region_name: 17
source: dbSNP
start: 73342622
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342623
feature_type: variation
id: rs2062448865
seq_region_name: 17
source: dbSNP
start: 73342623
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342624
feature_type: variation
id: rs1599465707
seq_region_name: 17
source: dbSNP
start: 73342624
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342627
feature_type: variation
id: rs2062448919
seq_region_name: 17
source: dbSNP
start: 73342627
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs967628119
seq_region_name: 17
source: dbSNP
start: 73342630
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs964666275
seq_region_name: 17
source: dbSNP
start: 73342640
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145372831
seq_region_name: 17
source: dbSNP
start: 73342642
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342646
feature_type: variation
id: rs1599465712
seq_region_name: 17
source: dbSNP
start: 73342646
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342647
feature_type: variation
id: rs1237136663
seq_region_name: 17
source: dbSNP
start: 73342647
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342649
feature_type: variation
id: rs2145372860
seq_region_name: 17
source: dbSNP
start: 73342649
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342650
feature_type: variation
id: rs2062449049
seq_region_name: 17
source: dbSNP
start: 73342650
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342653
feature_type: variation
id: rs1599465716
seq_region_name: 17
source: dbSNP
start: 73342653
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342655
feature_type: variation
id: rs999532015
seq_region_name: 17
source: dbSNP
start: 73342655
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73342656
feature_type: variation
id: rs2145372897
seq_region_name: 17
source: dbSNP
start: 73342656
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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source: dbSNP
start: 73342880
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assembly_name: GRCh38
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start: 73342884
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73342885
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73342889
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73342897
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73343042
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73343054
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73343070
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73343071
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73343078
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343082
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343084
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343093
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73343096
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343097
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343100
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343101
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343103
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062453230
seq_region_name: 17
source: dbSNP
start: 73343105
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73343125
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1423541804
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1273763337
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343141
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs934655363
seq_region_name: 17
source: dbSNP
start: 73343142
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1054484909
seq_region_name: 17
source: dbSNP
start: 73343143
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062453689
seq_region_name: 17
source: dbSNP
start: 73343148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062453731
seq_region_name: 17
source: dbSNP
start: 73343149
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1167254197
seq_region_name: 17
source: dbSNP
start: 73343154
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062453803
seq_region_name: 17
source: dbSNP
start: 73343155
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1301671891
seq_region_name: 17
source: dbSNP
start: 73343160
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1388810961
seq_region_name: 17
source: dbSNP
start: 73343161
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062453913
seq_region_name: 17
source: dbSNP
start: 73343163
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062453946
seq_region_name: 17
source: dbSNP
start: 73343165
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062453978
seq_region_name: 17
source: dbSNP
start: 73343167
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs893373929
seq_region_name: 17
source: dbSNP
start: 73343168
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062454015
seq_region_name: 17
source: dbSNP
start: 73343171
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343179
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062454108
seq_region_name: 17
source: dbSNP
start: 73343182
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1007776186
seq_region_name: 17
source: dbSNP
start: 73343186
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062454188
seq_region_name: 17
source: dbSNP
start: 73343187
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343188
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062454256
seq_region_name: 17
source: dbSNP
start: 73343190
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1406548238
seq_region_name: 17
source: dbSNP
start: 73343197
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs760005680
seq_region_name: 17
source: dbSNP
start: 73343204
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145374707
seq_region_name: 17
source: dbSNP
start: 73343204
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062454389
seq_region_name: 17
source: dbSNP
start: 73343205
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343207
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1393681064
seq_region_name: 17
source: dbSNP
start: 73343209
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs537665717
seq_region_name: 17
source: dbSNP
start: 73343220
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1346685756
seq_region_name: 17
source: dbSNP
start: 73343222
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343223
feature_type: variation
id: rs2062454500
seq_region_name: 17
source: dbSNP
start: 73343223
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343226
feature_type: variation
id: rs549304165
seq_region_name: 17
source: dbSNP
start: 73343226
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343228
feature_type: variation
id: rs1277480298
seq_region_name: 17
source: dbSNP
start: 73343228
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343230
feature_type: variation
id: rs2062454579
seq_region_name: 17
source: dbSNP
start: 73343230
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343232
feature_type: variation
id: rs2062454601
seq_region_name: 17
source: dbSNP
start: 73343232
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343233
feature_type: variation
id: rs2062454622
seq_region_name: 17
source: dbSNP
start: 73343233
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343241
feature_type: variation
id: rs567600888
seq_region_name: 17
source: dbSNP
start: 73343241
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343243
feature_type: variation
id: rs1029825680
seq_region_name: 17
source: dbSNP
start: 73343243
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343245
feature_type: variation
id: rs1234567463
seq_region_name: 17
source: dbSNP
start: 73343245
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343246
feature_type: variation
id: rs2062454722
seq_region_name: 17
source: dbSNP
start: 73343246
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343247
feature_type: variation
id: rs951188722
seq_region_name: 17
source: dbSNP
start: 73343247
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343249
feature_type: variation
id: rs2062454769
seq_region_name: 17
source: dbSNP
start: 73343249
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343251
feature_type: variation
id: rs924596127
seq_region_name: 17
source: dbSNP
start: 73343251
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343252
feature_type: variation
id: rs1272335134
seq_region_name: 17
source: dbSNP
start: 73343252
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343255
feature_type: variation
id: rs2062454832
seq_region_name: 17
source: dbSNP
start: 73343255
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343256
feature_type: variation
id: rs538464049
seq_region_name: 17
source: dbSNP
start: 73343256
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343262
feature_type: variation
id: rs955982049
seq_region_name: 17
source: dbSNP
start: 73343262
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343264
feature_type: variation
id: rs990037231
seq_region_name: 17
source: dbSNP
start: 73343264
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343267
feature_type: variation
id: rs1960707147
seq_region_name: 17
source: dbSNP
start: 73343267
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs982844400
seq_region_name: 17
source: dbSNP
start: 73343269
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343273
feature_type: variation
id: rs2062454928
seq_region_name: 17
source: dbSNP
start: 73343269
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343270
feature_type: variation
id: rs1372193564
seq_region_name: 17
source: dbSNP
start: 73343270
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343271
feature_type: variation
id: rs2062454954
seq_region_name: 17
source: dbSNP
start: 73343271
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343272
feature_type: variation
id: rs1599466302
seq_region_name: 17
source: dbSNP
start: 73343272
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343273
feature_type: variation
id: rs759061255
seq_region_name: 17
source: dbSNP
start: 73343273
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343276
feature_type: variation
id: rs1422254853
seq_region_name: 17
source: dbSNP
start: 73343276
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343282
feature_type: variation
id: rs1223942299
seq_region_name: 17
source: dbSNP
start: 73343282
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343284
feature_type: variation
id: rs867556310
seq_region_name: 17
source: dbSNP
start: 73343284
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343288
feature_type: variation
id: rs2062455086
seq_region_name: 17
source: dbSNP
start: 73343288
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343292
feature_type: variation
id: rs1016624208
seq_region_name: 17
source: dbSNP
start: 73343292
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343293
feature_type: variation
id: rs1327579489
seq_region_name: 17
source: dbSNP
start: 73343293
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343294
feature_type: variation
id: rs1429857312
seq_region_name: 17
source: dbSNP
start: 73343294
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343295
feature_type: variation
id: rs962597145
seq_region_name: 17
source: dbSNP
start: 73343295
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343295
feature_type: variation
id: rs1568357911
seq_region_name: 17
source: dbSNP
start: 73343295
strand: 1
-
alleles:
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- GAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343299
feature_type: variation
id: rs1371979943
seq_region_name: 17
source: dbSNP
start: 73343295
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343296
feature_type: variation
id: rs2062455250
seq_region_name: 17
source: dbSNP
start: 73343296
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343300
feature_type: variation
id: rs1599466340
seq_region_name: 17
source: dbSNP
start: 73343300
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343301
feature_type: variation
id: rs2145375092
seq_region_name: 17
source: dbSNP
start: 73343301
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343302
feature_type: variation
id: rs2062455290
seq_region_name: 17
source: dbSNP
start: 73343302
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343303
feature_type: variation
id: rs2062455314
seq_region_name: 17
source: dbSNP
start: 73343303
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343305
feature_type: variation
id: rs1433806455
seq_region_name: 17
source: dbSNP
start: 73343305
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343307
feature_type: variation
id: rs2062455384
seq_region_name: 17
source: dbSNP
start: 73343307
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343309
feature_type: variation
id: rs2062455408
seq_region_name: 17
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs537103443
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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start: 73343329
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343343
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343348
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1005867329
seq_region_name: 17
source: dbSNP
start: 73343349
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1359429674
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- CTGCTGCTGCT
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343395
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343396
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343397
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343406
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1211547108
seq_region_name: 17
source: dbSNP
start: 73343407
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343412
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343412
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343415
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343416
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs934788346
seq_region_name: 17
source: dbSNP
start: 73343417
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343419
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062456547
seq_region_name: 17
source: dbSNP
start: 73343420
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145375538
seq_region_name: 17
source: dbSNP
start: 73343421
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1054833336
seq_region_name: 17
source: dbSNP
start: 73343422
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1031686423
seq_region_name: 17
source: dbSNP
start: 73343423
strand: 1
-
alleles:
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- GAGAAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003355758
seq_region_name: 17
source: dbSNP
start: 73343423
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs893154741
seq_region_name: 17
source: dbSNP
start: 73343425
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1424507414
seq_region_name: 17
source: dbSNP
start: 73343426
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062456685
seq_region_name: 17
source: dbSNP
start: 73343427
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145375582
seq_region_name: 17
source: dbSNP
start: 73343437
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs956057084
seq_region_name: 17
source: dbSNP
start: 73343438
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs943583395
seq_region_name: 17
source: dbSNP
start: 73343439
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343441
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062456795
seq_region_name: 17
source: dbSNP
start: 73343441
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs964984915
seq_region_name: 17
source: dbSNP
start: 73343442
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062456840
seq_region_name: 17
source: dbSNP
start: 73343444
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343445
feature_type: variation
id: rs974628793
seq_region_name: 17
source: dbSNP
start: 73343445
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1467487664
seq_region_name: 17
source: dbSNP
start: 73343450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062456901
seq_region_name: 17
source: dbSNP
start: 73343455
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1442391142
seq_region_name: 17
source: dbSNP
start: 73343460
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73343467
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs866181275
seq_region_name: 17
source: dbSNP
start: 73343471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062456988
seq_region_name: 17
source: dbSNP
start: 73343472
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062457015
seq_region_name: 17
source: dbSNP
start: 73343473
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343474
feature_type: variation
id: rs2062457050
seq_region_name: 17
source: dbSNP
start: 73343474
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343477
feature_type: variation
id: rs2062457077
seq_region_name: 17
source: dbSNP
start: 73343477
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs554262742
seq_region_name: 17
source: dbSNP
start: 73343481
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343486
feature_type: variation
id: rs933140342
seq_region_name: 17
source: dbSNP
start: 73343486
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343488
feature_type: variation
id: rs1314317409
seq_region_name: 17
source: dbSNP
start: 73343488
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343489
feature_type: variation
id: rs1238393398
seq_region_name: 17
source: dbSNP
start: 73343489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343494
feature_type: variation
id: rs2062457233
seq_region_name: 17
source: dbSNP
start: 73343494
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343503
feature_type: variation
id: rs2062457252
seq_region_name: 17
source: dbSNP
start: 73343503
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343506
feature_type: variation
id: rs2062457277
seq_region_name: 17
source: dbSNP
start: 73343506
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73343508
feature_type: variation
id: rs572520730
seq_region_name: 17
source: dbSNP
start: 73343508
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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- "-"
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73343752
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73343754
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73343755
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73343758
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73343759
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344001
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alleles:
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alleles:
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alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73344104
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344109
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73344116
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344120
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73344126
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73344134
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73344135
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73344137
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344142
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73344143
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344153
strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs996155152
seq_region_name: 17
source: dbSNP
start: 73344156
strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs1030673460
seq_region_name: 17
source: dbSNP
start: 73344161
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73344163
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344164
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs536716400
seq_region_name: 17
source: dbSNP
start: 73344172
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1037895282
seq_region_name: 17
source: dbSNP
start: 73344173
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1337642061
seq_region_name: 17
source: dbSNP
start: 73344177
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs898233061
seq_region_name: 17
source: dbSNP
start: 73344178
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1229518651
seq_region_name: 17
source: dbSNP
start: 73344179
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1477201539
seq_region_name: 17
source: dbSNP
start: 73344180
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344185
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344186
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1367776141
seq_region_name: 17
source: dbSNP
start: 73344190
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062463329
seq_region_name: 17
source: dbSNP
start: 73344191
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344193
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062463388
seq_region_name: 17
source: dbSNP
start: 73344194
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568358329
seq_region_name: 17
source: dbSNP
start: 73344200
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062463443
seq_region_name: 17
source: dbSNP
start: 73344208
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1012682332
seq_region_name: 17
source: dbSNP
start: 73344211
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344220
feature_type: variation
id: rs1332222886
seq_region_name: 17
source: dbSNP
start: 73344220
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73344224
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344224
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344225
feature_type: variation
id: rs185647289
seq_region_name: 17
source: dbSNP
start: 73344225
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344226
feature_type: variation
id: rs2062463568
seq_region_name: 17
source: dbSNP
start: 73344226
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344231
feature_type: variation
id: rs2062463594
seq_region_name: 17
source: dbSNP
start: 73344231
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344234
feature_type: variation
id: rs1475182891
seq_region_name: 17
source: dbSNP
start: 73344234
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344237
feature_type: variation
id: rs2062463644
seq_region_name: 17
source: dbSNP
start: 73344237
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344238
feature_type: variation
id: rs1368251195
seq_region_name: 17
source: dbSNP
start: 73344238
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344246
feature_type: variation
id: rs2145377909
seq_region_name: 17
source: dbSNP
start: 73344246
strand: 1
-
alleles:
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- T
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs540809658
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73344303
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs559048129
seq_region_name: 17
source: dbSNP
start: 73344305
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344308
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062464202
seq_region_name: 17
source: dbSNP
start: 73344310
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs574218197
seq_region_name: 17
source: dbSNP
start: 73344315
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344316
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344317
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344318
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73344329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73344331
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs908099120
seq_region_name: 17
source: dbSNP
start: 73344340
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344341
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344350
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73344355
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344356
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1329122376
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599467148
seq_region_name: 17
source: dbSNP
start: 73344365
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344366
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344366
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs758435293
seq_region_name: 17
source: dbSNP
start: 73344370
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs973537267
seq_region_name: 17
source: dbSNP
start: 73344377
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062464926
seq_region_name: 17
source: dbSNP
start: 73344380
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344385
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs947533791
seq_region_name: 17
source: dbSNP
start: 73344387
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344394
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs75303415
seq_region_name: 17
source: dbSNP
start: 73344395
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062465083
seq_region_name: 17
source: dbSNP
start: 73344399
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145378372
seq_region_name: 17
source: dbSNP
start: 73344400
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145378379
seq_region_name: 17
source: dbSNP
start: 73344403
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs543675201
seq_region_name: 17
source: dbSNP
start: 73344409
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344410
feature_type: variation
id: rs550255480
seq_region_name: 17
source: dbSNP
start: 73344410
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344412
feature_type: variation
id: rs1335979594
seq_region_name: 17
source: dbSNP
start: 73344412
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344413
feature_type: variation
id: rs2062465166
seq_region_name: 17
source: dbSNP
start: 73344413
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344415
feature_type: variation
id: rs1599467173
seq_region_name: 17
source: dbSNP
start: 73344415
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565563677
seq_region_name: 17
source: dbSNP
start: 73344421
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344423
feature_type: variation
id: rs2062465240
seq_region_name: 17
source: dbSNP
start: 73344423
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344424
feature_type: variation
id: rs2062465268
seq_region_name: 17
source: dbSNP
start: 73344424
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344426
feature_type: variation
id: rs189291706
seq_region_name: 17
source: dbSNP
start: 73344426
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344427
feature_type: variation
id: rs1159947974
seq_region_name: 17
source: dbSNP
start: 73344427
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344429
feature_type: variation
id: rs906979293
seq_region_name: 17
source: dbSNP
start: 73344429
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344431
feature_type: variation
id: rs1411828988
seq_region_name: 17
source: dbSNP
start: 73344431
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344437
feature_type: variation
id: rs2062465487
seq_region_name: 17
source: dbSNP
start: 73344437
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344439
feature_type: variation
id: rs2062465528
seq_region_name: 17
source: dbSNP
start: 73344439
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344441
feature_type: variation
id: rs1004788398
seq_region_name: 17
source: dbSNP
start: 73344441
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344444
feature_type: variation
id: rs2062465615
seq_region_name: 17
source: dbSNP
start: 73344444
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344451
feature_type: variation
id: rs1014819109
seq_region_name: 17
source: dbSNP
start: 73344451
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344453
feature_type: variation
id: rs1473289880
seq_region_name: 17
source: dbSNP
start: 73344453
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344457
feature_type: variation
id: rs1239551232
seq_region_name: 17
source: dbSNP
start: 73344457
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344464
feature_type: variation
id: rs1207281656
seq_region_name: 17
source: dbSNP
start: 73344464
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344465
feature_type: variation
id: rs770433672
seq_region_name: 17
source: dbSNP
start: 73344465
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344467
feature_type: variation
id: rs1053227508
seq_region_name: 17
source: dbSNP
start: 73344467
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344471
feature_type: variation
id: rs1269356735
seq_region_name: 17
source: dbSNP
start: 73344471
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344473
feature_type: variation
id: rs1208736924
seq_region_name: 17
source: dbSNP
start: 73344473
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344473
feature_type: variation
id: rs2062465850
seq_region_name: 17
source: dbSNP
start: 73344473
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344476
feature_type: variation
id: rs994632976
seq_region_name: 17
source: dbSNP
start: 73344476
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344481
feature_type: variation
id: rs2062465943
seq_region_name: 17
source: dbSNP
start: 73344481
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344489
feature_type: variation
id: rs2062465967
seq_region_name: 17
source: dbSNP
start: 73344489
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344678
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73344688
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73344701
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73344702
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344703
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344704
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344705
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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id: rs916715899
seq_region_name: 17
source: dbSNP
start: 73344711
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344712
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs868633240
seq_region_name: 17
source: dbSNP
start: 73344720
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062467934
seq_region_name: 17
source: dbSNP
start: 73344725
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344727
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344728
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344732
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344733
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344736
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs558611286
seq_region_name: 17
source: dbSNP
start: 73344740
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs982726357
seq_region_name: 17
source: dbSNP
start: 73344741
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344742
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id: rs180804897
seq_region_name: 17
source: dbSNP
start: 73344742
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344744
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id: rs2145379122
seq_region_name: 17
source: dbSNP
start: 73344744
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344745
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id: rs577043096
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strand: 1
-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs763407693
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062468674
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs769210755
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1378793302
seq_region_name: 17
source: dbSNP
start: 73344814
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062468792
seq_region_name: 17
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start: 73344816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs994706359
seq_region_name: 17
source: dbSNP
start: 73344818
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344822
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1177404370
seq_region_name: 17
source: dbSNP
start: 73344825
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344828
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1003308826
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344868
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344870
strand: 1
-
alleles:
- CCTGCACGC
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344877
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344878
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73344883
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344886
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73344888
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062469474
seq_region_name: 17
source: dbSNP
start: 73344889
strand: 1
-
alleles:
- CCC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344899
feature_type: variation
id: rs2062469499
seq_region_name: 17
source: dbSNP
start: 73344897
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs987736068
seq_region_name: 17
source: dbSNP
start: 73344902
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145379451
seq_region_name: 17
source: dbSNP
start: 73344903
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062469560
seq_region_name: 17
source: dbSNP
start: 73344905
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1374184668
seq_region_name: 17
source: dbSNP
start: 73344907
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062469632
seq_region_name: 17
source: dbSNP
start: 73344911
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344914
feature_type: variation
id: rs2062469662
seq_region_name: 17
source: dbSNP
start: 73344914
strand: 1
-
alleles:
- TTT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344916
feature_type: variation
id: rs2062469683
seq_region_name: 17
source: dbSNP
start: 73344914
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344915
feature_type: variation
id: rs2062469700
seq_region_name: 17
source: dbSNP
start: 73344915
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344917
feature_type: variation
id: rs1449213150
seq_region_name: 17
source: dbSNP
start: 73344917
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062469756
seq_region_name: 17
source: dbSNP
start: 73344919
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1020530228
seq_region_name: 17
source: dbSNP
start: 73344920
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs968941761
seq_region_name: 17
source: dbSNP
start: 73344927
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344929
feature_type: variation
id: rs2062469837
seq_region_name: 17
source: dbSNP
start: 73344929
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344931
feature_type: variation
id: rs2062469859
seq_region_name: 17
source: dbSNP
start: 73344931
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344932
feature_type: variation
id: rs1471232011
seq_region_name: 17
source: dbSNP
start: 73344932
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344934
feature_type: variation
id: rs1387122943
seq_region_name: 17
source: dbSNP
start: 73344934
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344937
feature_type: variation
id: rs2062469899
seq_region_name: 17
source: dbSNP
start: 73344937
strand: 1
-
alleles:
- GCCACCTCCTTCAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344950
feature_type: variation
id: rs1052848266
seq_region_name: 17
source: dbSNP
start: 73344937
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344938
feature_type: variation
id: rs1021656
seq_region_name: 17
source: dbSNP
start: 73344938
strand: 1
-
alleles:
- CC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344939
feature_type: variation
id: rs2062469977
seq_region_name: 17
source: dbSNP
start: 73344938
strand: 1
-
alleles:
- CCTCCTTCAGGC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344952
feature_type: variation
id: rs2062470008
seq_region_name: 17
source: dbSNP
start: 73344941
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344947
feature_type: variation
id: rs2062470033
seq_region_name: 17
source: dbSNP
start: 73344947
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344948
feature_type: variation
id: rs2062470053
seq_region_name: 17
source: dbSNP
start: 73344948
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344949
feature_type: variation
id: rs1412177810
seq_region_name: 17
source: dbSNP
start: 73344949
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344951
feature_type: variation
id: rs932112583
seq_region_name: 17
source: dbSNP
start: 73344951
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344955
feature_type: variation
id: rs1421727551
seq_region_name: 17
source: dbSNP
start: 73344955
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344957
feature_type: variation
id: rs1375785972
seq_region_name: 17
source: dbSNP
start: 73344957
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344961
feature_type: variation
id: rs2062470186
seq_region_name: 17
source: dbSNP
start: 73344961
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344962
feature_type: variation
id: rs987590144
seq_region_name: 17
source: dbSNP
start: 73344962
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344966
feature_type: variation
id: rs2062470243
seq_region_name: 17
source: dbSNP
start: 73344966
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344973
feature_type: variation
id: rs1599467555
seq_region_name: 17
source: dbSNP
start: 73344973
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73344975
feature_type: variation
id: rs2062470290
seq_region_name: 17
source: dbSNP
start: 73344975
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345094
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73345108
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345115
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345124
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73345130
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345133
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345137
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345142
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345144
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345147
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345148
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345149
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345152
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062471961
seq_region_name: 17
source: dbSNP
start: 73345154
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345155
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062472015
seq_region_name: 17
source: dbSNP
start: 73345156
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345157
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345160
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345162
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345166
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345168
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345173
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs138181630
seq_region_name: 17
source: dbSNP
start: 73345175
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1196766054
seq_region_name: 17
source: dbSNP
start: 73345176
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs570725239
seq_region_name: 17
source: dbSNP
start: 73345177
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345178
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1269768769
seq_region_name: 17
source: dbSNP
start: 73345179
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345181
feature_type: variation
id: rs1296215905
seq_region_name: 17
source: dbSNP
start: 73345181
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345184
feature_type: variation
id: rs534615382
seq_region_name: 17
source: dbSNP
start: 73345184
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345188
feature_type: variation
id: rs1482220732
seq_region_name: 17
source: dbSNP
start: 73345188
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345189
feature_type: variation
id: rs1274303699
seq_region_name: 17
source: dbSNP
start: 73345189
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345193
feature_type: variation
id: rs968972949
seq_region_name: 17
source: dbSNP
start: 73345193
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345195
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1303273305
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1036440388
seq_region_name: 17
source: dbSNP
start: 73345234
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062472931
seq_region_name: 17
source: dbSNP
start: 73345254
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345255
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs567962384
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1223358434
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345281
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1410329139
seq_region_name: 17
source: dbSNP
start: 73345284
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs899286958
seq_region_name: 17
source: dbSNP
start: 73345286
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1170732998
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345295
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345298
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345305
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345306
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345307
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345311
strand: 1
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alleles:
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- G
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73345316
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73345319
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345320
strand: 1
-
alleles:
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- AAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs532451680
seq_region_name: 17
source: dbSNP
start: 73345320
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345320
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345322
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345324
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345325
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345328
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73345329
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1442567705
seq_region_name: 17
source: dbSNP
start: 73345330
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73345331
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345334
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345336
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062473925
seq_region_name: 17
source: dbSNP
start: 73345337
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1411396792
seq_region_name: 17
source: dbSNP
start: 73345338
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs766520876
seq_region_name: 17
source: dbSNP
start: 73345345
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345348
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062474029
seq_region_name: 17
source: dbSNP
start: 73345351
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345368
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs988368156
seq_region_name: 17
source: dbSNP
start: 73345371
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145380605
seq_region_name: 17
source: dbSNP
start: 73345373
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1236063327
seq_region_name: 17
source: dbSNP
start: 73345374
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1187310388
seq_region_name: 17
source: dbSNP
start: 73345376
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs114275090
seq_region_name: 17
source: dbSNP
start: 73345377
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345381
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345382
feature_type: variation
id: rs2062474204
seq_region_name: 17
source: dbSNP
start: 73345382
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1265549373
seq_region_name: 17
source: dbSNP
start: 73345384
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345388
feature_type: variation
id: rs2062474264
seq_region_name: 17
source: dbSNP
start: 73345388
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs939236038
seq_region_name: 17
source: dbSNP
start: 73345392
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345405
feature_type: variation
id: rs2145380658
seq_region_name: 17
source: dbSNP
start: 73345405
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345413
feature_type: variation
id: rs1056226727
seq_region_name: 17
source: dbSNP
start: 73345413
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345414
feature_type: variation
id: rs892240701
seq_region_name: 17
source: dbSNP
start: 73345414
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345424
feature_type: variation
id: rs2062474369
seq_region_name: 17
source: dbSNP
start: 73345424
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345425
feature_type: variation
id: rs545553079
seq_region_name: 17
source: dbSNP
start: 73345425
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345429
feature_type: variation
id: rs1009259628
seq_region_name: 17
source: dbSNP
start: 73345429
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345430
feature_type: variation
id: rs557743776
seq_region_name: 17
source: dbSNP
start: 73345430
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345431
feature_type: variation
id: rs1216218589
seq_region_name: 17
source: dbSNP
start: 73345431
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345432
feature_type: variation
id: rs1599467902
seq_region_name: 17
source: dbSNP
start: 73345432
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345437
feature_type: variation
id: rs377291597
seq_region_name: 17
source: dbSNP
start: 73345437
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345441
feature_type: variation
id: rs903535136
seq_region_name: 17
source: dbSNP
start: 73345441
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345443
feature_type: variation
id: rs996873746
seq_region_name: 17
source: dbSNP
start: 73345443
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345450
feature_type: variation
id: rs2062474601
seq_region_name: 17
source: dbSNP
start: 73345450
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345453
feature_type: variation
id: rs543626360
seq_region_name: 17
source: dbSNP
start: 73345453
strand: 1
-
alleles:
- ATATTATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345464
feature_type: variation
id: rs1387958403
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345570
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345575
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345577
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145381115
seq_region_name: 17
source: dbSNP
start: 73345579
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1003583190
seq_region_name: 17
source: dbSNP
start: 73345582
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345585
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs939249087
seq_region_name: 17
source: dbSNP
start: 73345587
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345589
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs186829777
seq_region_name: 17
source: dbSNP
start: 73345590
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs751509445
seq_region_name: 17
source: dbSNP
start: 73345592
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062476118
seq_region_name: 17
source: dbSNP
start: 73345593
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1035681308
seq_region_name: 17
source: dbSNP
start: 73345594
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1297520282
seq_region_name: 17
source: dbSNP
start: 73345595
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062476206
seq_region_name: 17
source: dbSNP
start: 73345596
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1490425573
seq_region_name: 17
source: dbSNP
start: 73345598
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345600
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062476268
seq_region_name: 17
source: dbSNP
start: 73345601
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293608853
seq_region_name: 17
source: dbSNP
start: 73345602
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs531047854
seq_region_name: 17
source: dbSNP
start: 73345605
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1056257664
seq_region_name: 17
source: dbSNP
start: 73345608
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062476369
seq_region_name: 17
source: dbSNP
start: 73345609
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345610
feature_type: variation
id: rs913752583
seq_region_name: 17
source: dbSNP
start: 73345610
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1306783120
seq_region_name: 17
source: dbSNP
start: 73345612
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345615
feature_type: variation
id: rs2062476459
seq_region_name: 17
source: dbSNP
start: 73345615
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345623
feature_type: variation
id: rs2062476495
seq_region_name: 17
source: dbSNP
start: 73345623
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345627
feature_type: variation
id: rs2062476526
seq_region_name: 17
source: dbSNP
start: 73345627
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345630
feature_type: variation
id: rs892743352
seq_region_name: 17
source: dbSNP
start: 73345630
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345639
feature_type: variation
id: rs2062476556
seq_region_name: 17
source: dbSNP
start: 73345634
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345636
feature_type: variation
id: rs1009679957
seq_region_name: 17
source: dbSNP
start: 73345636
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345637
feature_type: variation
id: rs2062476590
seq_region_name: 17
source: dbSNP
start: 73345637
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345638
feature_type: variation
id: rs376185431
seq_region_name: 17
source: dbSNP
start: 73345638
strand: 1
-
alleles:
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- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345642
feature_type: variation
id: rs2062476648
seq_region_name: 17
source: dbSNP
start: 73345639
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345644
feature_type: variation
id: rs1405762151
seq_region_name: 17
source: dbSNP
start: 73345644
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345650
feature_type: variation
id: rs2062476707
seq_region_name: 17
source: dbSNP
start: 73345650
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345653
feature_type: variation
id: rs1367711862
seq_region_name: 17
source: dbSNP
start: 73345653
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345654
feature_type: variation
id: rs2062476774
seq_region_name: 17
source: dbSNP
start: 73345654
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345655
feature_type: variation
id: rs2145381360
seq_region_name: 17
source: dbSNP
start: 73345655
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345656
feature_type: variation
id: rs1306520240
seq_region_name: 17
source: dbSNP
start: 73345656
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73345802
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345816
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345819
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345822
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345824
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345825
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345827
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73345828
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345830
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345842
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73345849
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345851
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73345856
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345857
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345858
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345859
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345866
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73345873
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345875
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345880
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345881
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345884
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73345887
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs892684540
seq_region_name: 17
source: dbSNP
start: 73345889
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73345890
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345892
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345895
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345898
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73345900
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs913780431
seq_region_name: 17
source: dbSNP
start: 73345902
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345903
feature_type: variation
id: rs1009790855
seq_region_name: 17
source: dbSNP
start: 73345903
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1022379624
seq_region_name: 17
source: dbSNP
start: 73345905
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062478908
seq_region_name: 17
source: dbSNP
start: 73345908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345914
feature_type: variation
id: rs2062478934
seq_region_name: 17
source: dbSNP
start: 73345914
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345917
feature_type: variation
id: rs1337949455
seq_region_name: 17
source: dbSNP
start: 73345914
strand: 1
-
alleles:
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- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345920
feature_type: variation
id: rs141352246
seq_region_name: 17
source: dbSNP
start: 73345916
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345917
feature_type: variation
id: rs2062479024
seq_region_name: 17
source: dbSNP
start: 73345917
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345918
feature_type: variation
id: rs779472237
seq_region_name: 17
source: dbSNP
start: 73345918
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73345921
feature_type: variation
id: rs2062479093
seq_region_name: 17
source: dbSNP
start: 73345921
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73346097
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73346105
strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73346137
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73346140
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73346141
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346142
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73346143
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346144
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346145
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346148
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73346152
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346153
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346155
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346160
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs557563739
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73346165
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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id: rs771245048
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source: dbSNP
start: 73346170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346173
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599468462
seq_region_name: 17
source: dbSNP
start: 73346175
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062482376
seq_region_name: 17
source: dbSNP
start: 73346180
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs553729657
seq_region_name: 17
source: dbSNP
start: 73346189
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs200933954
seq_region_name: 17
source: dbSNP
start: 73346190
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1219386188
seq_region_name: 17
source: dbSNP
start: 73346191
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599468476
seq_region_name: 17
source: dbSNP
start: 73346192
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1225117524
seq_region_name: 17
source: dbSNP
start: 73346195
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599468481
seq_region_name: 17
source: dbSNP
start: 73346196
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062482606
seq_region_name: 17
source: dbSNP
start: 73346201
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062482646
seq_region_name: 17
source: dbSNP
start: 73346203
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1482273039
seq_region_name: 17
source: dbSNP
start: 73346204
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1272789352
seq_region_name: 17
source: dbSNP
start: 73346208
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062482709
seq_region_name: 17
source: dbSNP
start: 73346209
strand: 1
-
alleles:
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- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062482758
seq_region_name: 17
source: dbSNP
start: 73346209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1040357160
seq_region_name: 17
source: dbSNP
start: 73346211
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1283509359
seq_region_name: 17
source: dbSNP
start: 73346212
strand: 1
-
alleles:
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- AAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs966595517
seq_region_name: 17
source: dbSNP
start: 73346212
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1406460207
seq_region_name: 17
source: dbSNP
start: 73346214
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs888832881
seq_region_name: 17
source: dbSNP
start: 73346219
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1327990610
seq_region_name: 17
source: dbSNP
start: 73346220
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs979258725
seq_region_name: 17
source: dbSNP
start: 73346221
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483041
seq_region_name: 17
source: dbSNP
start: 73346222
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346222
strand: 1
-
alleles:
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- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1398588059
seq_region_name: 17
source: dbSNP
start: 73346223
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346224
strand: 1
-
alleles:
- AAAGAAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73346224
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062483187
seq_region_name: 17
source: dbSNP
start: 73346225
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346227
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1201858852
seq_region_name: 17
source: dbSNP
start: 73346228
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs542120616
seq_region_name: 17
source: dbSNP
start: 73346229
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483288
seq_region_name: 17
source: dbSNP
start: 73346231
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483311
seq_region_name: 17
source: dbSNP
start: 73346232
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs932193824
seq_region_name: 17
source: dbSNP
start: 73346233
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346234
feature_type: variation
id: rs2062483359
seq_region_name: 17
source: dbSNP
start: 73346234
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1050656012
seq_region_name: 17
source: dbSNP
start: 73346238
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1232611403
seq_region_name: 17
source: dbSNP
start: 73346239
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1008651049
seq_region_name: 17
source: dbSNP
start: 73346242
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1018993290
seq_region_name: 17
source: dbSNP
start: 73346243
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483493
seq_region_name: 17
source: dbSNP
start: 73346244
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062483516
seq_region_name: 17
source: dbSNP
start: 73346246
strand: 1
-
alleles:
- CTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483548
seq_region_name: 17
source: dbSNP
start: 73346247
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062483571
seq_region_name: 17
source: dbSNP
start: 73346248
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483607
seq_region_name: 17
source: dbSNP
start: 73346250
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062483646
seq_region_name: 17
source: dbSNP
start: 73346250
strand: 1
-
alleles:
- A
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346255
feature_type: variation
id: rs7220853
seq_region_name: 17
source: dbSNP
start: 73346255
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs985618325
seq_region_name: 17
source: dbSNP
start: 73346257
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346259
feature_type: variation
id: rs2062483847
seq_region_name: 17
source: dbSNP
start: 73346259
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145383268
seq_region_name: 17
source: dbSNP
start: 73346262
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346266
feature_type: variation
id: rs2145383279
seq_region_name: 17
source: dbSNP
start: 73346266
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346272
feature_type: variation
id: rs2062483871
seq_region_name: 17
source: dbSNP
start: 73346272
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346275
feature_type: variation
id: rs912280381
seq_region_name: 17
source: dbSNP
start: 73346275
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346277
feature_type: variation
id: rs2062483926
seq_region_name: 17
source: dbSNP
start: 73346277
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346280
feature_type: variation
id: rs2062483958
seq_region_name: 17
source: dbSNP
start: 73346280
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346282
feature_type: variation
id: rs530963415
seq_region_name: 17
source: dbSNP
start: 73346282
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346290
feature_type: variation
id: rs1027556896
seq_region_name: 17
source: dbSNP
start: 73346290
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346291
feature_type: variation
id: rs2062484056
seq_region_name: 17
source: dbSNP
start: 73346291
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346292
feature_type: variation
id: rs368627775
seq_region_name: 17
source: dbSNP
start: 73346292
strand: 1
-
alleles:
- CAC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346294
feature_type: variation
id: rs2062484113
seq_region_name: 17
source: dbSNP
start: 73346292
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346292
feature_type: variation
id: rs2062484137
seq_region_name: 17
source: dbSNP
start: 73346293
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346293
feature_type: variation
id: rs1036697180
seq_region_name: 17
source: dbSNP
start: 73346293
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346294
feature_type: variation
id: rs7220304
seq_region_name: 17
source: dbSNP
start: 73346294
strand: 1
-
alleles:
- TT
- TTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346296
feature_type: variation
id: rs2062484262
seq_region_name: 17
source: dbSNP
start: 73346295
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346301
feature_type: variation
id: rs1568359311
seq_region_name: 17
source: dbSNP
start: 73346301
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346302
feature_type: variation
id: rs980986849
seq_region_name: 17
source: dbSNP
start: 73346302
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346303
feature_type: variation
id: rs926497265
seq_region_name: 17
source: dbSNP
start: 73346303
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346304
feature_type: variation
id: rs1599468596
seq_region_name: 17
source: dbSNP
start: 73346304
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346308
feature_type: variation
id: rs1049290330
seq_region_name: 17
source: dbSNP
start: 73346308
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346309
feature_type: variation
id: rs2062484479
seq_region_name: 17
source: dbSNP
start: 73346309
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346310
feature_type: variation
id: rs2062484508
seq_region_name: 17
source: dbSNP
start: 73346310
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346316
feature_type: variation
id: rs1334596852
seq_region_name: 17
source: dbSNP
start: 73346316
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346322
feature_type: variation
id: rs564233833
seq_region_name: 17
source: dbSNP
start: 73346322
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346325
feature_type: variation
id: rs2062484568
seq_region_name: 17
source: dbSNP
start: 73346325
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346327
feature_type: variation
id: rs992262287
seq_region_name: 17
source: dbSNP
start: 73346327
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346331
feature_type: variation
id: rs2062484613
seq_region_name: 17
source: dbSNP
start: 73346331
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346336
feature_type: variation
id: rs1002335847
seq_region_name: 17
source: dbSNP
start: 73346336
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346341
feature_type: variation
id: rs2062484695
seq_region_name: 17
source: dbSNP
start: 73346341
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346343
feature_type: variation
id: rs1034186398
seq_region_name: 17
source: dbSNP
start: 73346343
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346344
feature_type: variation
id: rs2062484751
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs932917205
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346384
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346392
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346400
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346402
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346407
strand: 1
-
alleles:
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- TTTTTTTTTTT
- TTTTTTTTTTTTT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs202087594
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs564240489
seq_region_name: 17
source: dbSNP
start: 73346412
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346413
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs569080595
seq_region_name: 17
source: dbSNP
start: 73346413
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346420
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346420
strand: 1
-
alleles:
- GTACAAAACTTGGGCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346420
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346422
strand: 1
-
alleles:
- ACAA
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346422
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346423
strand: 1
-
alleles:
- CT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346429
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- TCTTCTT
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346435
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346440
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346445
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346446
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs551534554
seq_region_name: 17
source: dbSNP
start: 73346454
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062485861
seq_region_name: 17
source: dbSNP
start: 73346458
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346459
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346464
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062485936
seq_region_name: 17
source: dbSNP
start: 73346466
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73346469
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1445726274
seq_region_name: 17
source: dbSNP
start: 73346474
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062486036
seq_region_name: 17
source: dbSNP
start: 73346475
strand: 1
-
alleles:
- AAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145383900
seq_region_name: 17
source: dbSNP
start: 73346480
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1387638074
seq_region_name: 17
source: dbSNP
start: 73346481
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346481
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1183043305
seq_region_name: 17
source: dbSNP
start: 73346485
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs566548758
seq_region_name: 17
source: dbSNP
start: 73346486
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs965107385
seq_region_name: 17
source: dbSNP
start: 73346490
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs759649113
seq_region_name: 17
source: dbSNP
start: 73346494
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs972422254
seq_region_name: 17
source: dbSNP
start: 73346498
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73346500
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062486313
seq_region_name: 17
source: dbSNP
start: 73346503
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145383995
seq_region_name: 17
source: dbSNP
start: 73346506
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346515
feature_type: variation
id: rs918270929
seq_region_name: 17
source: dbSNP
start: 73346506
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1027338381
seq_region_name: 17
source: dbSNP
start: 73346516
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062486384
seq_region_name: 17
source: dbSNP
start: 73346525
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs930944968
seq_region_name: 17
source: dbSNP
start: 73346527
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs951920681
seq_region_name: 17
source: dbSNP
start: 73346530
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1221465972
seq_region_name: 17
source: dbSNP
start: 73346534
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1359991090
seq_region_name: 17
source: dbSNP
start: 73346540
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746433089
seq_region_name: 17
source: dbSNP
start: 73346544
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346548
feature_type: variation
id: rs2062486552
seq_region_name: 17
source: dbSNP
start: 73346544
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1314753506
seq_region_name: 17
source: dbSNP
start: 73346547
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs117821252
seq_region_name: 17
source: dbSNP
start: 73346550
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346551
feature_type: variation
id: rs1033895099
seq_region_name: 17
source: dbSNP
start: 73346551
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346553
feature_type: variation
id: rs960561833
seq_region_name: 17
source: dbSNP
start: 73346553
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346555
feature_type: variation
id: rs2062486634
seq_region_name: 17
source: dbSNP
start: 73346555
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346556
feature_type: variation
id: rs992438329
seq_region_name: 17
source: dbSNP
start: 73346556
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346557
feature_type: variation
id: rs2062486683
seq_region_name: 17
source: dbSNP
start: 73346557
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346559
feature_type: variation
id: rs2062486711
seq_region_name: 17
source: dbSNP
start: 73346559
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346565
feature_type: variation
id: rs1599468792
seq_region_name: 17
source: dbSNP
start: 73346565
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346569
feature_type: variation
id: rs1599468797
seq_region_name: 17
source: dbSNP
start: 73346569
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346573
feature_type: variation
id: rs913968794
seq_region_name: 17
source: dbSNP
start: 73346573
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346574
feature_type: variation
id: rs867586835
seq_region_name: 17
source: dbSNP
start: 73346574
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346578
feature_type: variation
id: rs2062486840
seq_region_name: 17
source: dbSNP
start: 73346578
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346582
feature_type: variation
id: rs2062486865
seq_region_name: 17
source: dbSNP
start: 73346582
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73346584
feature_type: variation
id: rs1369895601
seq_region_name: 17
source: dbSNP
start: 73346584
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73347006
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73347011
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347018
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73347024
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347029
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347035
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347038
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347045
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73347047
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73347049
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73347053
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347055
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347059
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347063
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347065
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73347073
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73347075
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73347077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347078
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347080
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347084
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347087
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347090
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347095
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347097
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1019520515
seq_region_name: 17
source: dbSNP
start: 73347098
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1257191760
seq_region_name: 17
source: dbSNP
start: 73347101
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1364780552
seq_region_name: 17
source: dbSNP
start: 73347104
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347109
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347109
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347112
feature_type: variation
id: rs902347727
seq_region_name: 17
source: dbSNP
start: 73347112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347116
feature_type: variation
id: rs779667050
seq_region_name: 17
source: dbSNP
start: 73347116
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347117
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347122
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs2062491380
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs566634147
seq_region_name: 17
source: dbSNP
start: 73347127
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1371350056
seq_region_name: 17
source: dbSNP
start: 73347132
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs533880177
seq_region_name: 17
source: dbSNP
start: 73347133
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1481995873
seq_region_name: 17
source: dbSNP
start: 73347133
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs952489257
seq_region_name: 17
source: dbSNP
start: 73347136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs984215200
seq_region_name: 17
source: dbSNP
start: 73347137
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1490279386
seq_region_name: 17
source: dbSNP
start: 73347139
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568359670
seq_region_name: 17
source: dbSNP
start: 73347140
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs954300096
seq_region_name: 17
source: dbSNP
start: 73347141
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062491639
seq_region_name: 17
source: dbSNP
start: 73347142
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293038244
seq_region_name: 17
source: dbSNP
start: 73347143
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062491681
seq_region_name: 17
source: dbSNP
start: 73347147
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1440681514
seq_region_name: 17
source: dbSNP
start: 73347150
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062491735
seq_region_name: 17
source: dbSNP
start: 73347151
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1338029337
seq_region_name: 17
source: dbSNP
start: 73347153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1226093800
seq_region_name: 17
source: dbSNP
start: 73347154
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062491822
seq_region_name: 17
source: dbSNP
start: 73347156
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1340653708
seq_region_name: 17
source: dbSNP
start: 73347163
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1279668566
seq_region_name: 17
source: dbSNP
start: 73347164
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1402793035
seq_region_name: 17
source: dbSNP
start: 73347170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062491919
seq_region_name: 17
source: dbSNP
start: 73347176
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs551188624
seq_region_name: 17
source: dbSNP
start: 73347178
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062491986
seq_region_name: 17
source: dbSNP
start: 73347186
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347187
feature_type: variation
id: rs2062492012
seq_region_name: 17
source: dbSNP
start: 73347187
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347188
feature_type: variation
id: rs1862189896
seq_region_name: 17
source: dbSNP
start: 73347188
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062492037
seq_region_name: 17
source: dbSNP
start: 73347189
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568359694
seq_region_name: 17
source: dbSNP
start: 73347197
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs149031838
seq_region_name: 17
source: dbSNP
start: 73347203
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347206
feature_type: variation
id: rs1020052611
seq_region_name: 17
source: dbSNP
start: 73347206
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347214
feature_type: variation
id: rs2062492146
seq_region_name: 17
source: dbSNP
start: 73347214
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347218
feature_type: variation
id: rs2062492169
seq_region_name: 17
source: dbSNP
start: 73347218
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347220
feature_type: variation
id: rs2062492198
seq_region_name: 17
source: dbSNP
start: 73347220
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347221
feature_type: variation
id: rs2030622906
seq_region_name: 17
source: dbSNP
start: 73347221
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347222
feature_type: variation
id: rs2145385790
seq_region_name: 17
source: dbSNP
start: 73347222
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347228
feature_type: variation
id: rs2062492216
seq_region_name: 17
source: dbSNP
start: 73347228
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1388379397
seq_region_name: 17
source: dbSNP
start: 73347230
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347231
feature_type: variation
id: rs184838697
seq_region_name: 17
source: dbSNP
start: 73347231
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347233
feature_type: variation
id: rs1466187236
seq_region_name: 17
source: dbSNP
start: 73347233
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347234
feature_type: variation
id: rs2062492321
seq_region_name: 17
source: dbSNP
start: 73347234
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347236
feature_type: variation
id: rs972990237
seq_region_name: 17
source: dbSNP
start: 73347236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347247
feature_type: variation
id: rs1360901844
seq_region_name: 17
source: dbSNP
start: 73347247
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347251
feature_type: variation
id: rs764754433
seq_region_name: 17
source: dbSNP
start: 73347251
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347252
feature_type: variation
id: rs2062492435
seq_region_name: 17
source: dbSNP
start: 73347252
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347253
feature_type: variation
id: rs2062492470
seq_region_name: 17
source: dbSNP
start: 73347253
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347255
feature_type: variation
id: rs567305283
seq_region_name: 17
source: dbSNP
start: 73347255
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347258
feature_type: variation
id: rs1336303988
seq_region_name: 17
source: dbSNP
start: 73347258
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347259
feature_type: variation
id: rs2062492550
seq_region_name: 17
source: dbSNP
start: 73347259
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347262
feature_type: variation
id: rs537436306
seq_region_name: 17
source: dbSNP
start: 73347262
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347267
feature_type: variation
id: rs188555055
seq_region_name: 17
source: dbSNP
start: 73347267
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347268
feature_type: variation
id: rs1250411512
seq_region_name: 17
source: dbSNP
start: 73347268
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347270
feature_type: variation
id: rs2062492672
seq_region_name: 17
source: dbSNP
start: 73347270
strand: 1
-
alleles:
- AA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347272
feature_type: variation
id: rs2062492694
seq_region_name: 17
source: dbSNP
start: 73347271
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347282
feature_type: variation
id: rs1196930227
seq_region_name: 17
source: dbSNP
start: 73347282
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347283
feature_type: variation
id: rs2062492722
seq_region_name: 17
source: dbSNP
start: 73347283
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347285
feature_type: variation
id: rs984310918
seq_region_name: 17
source: dbSNP
start: 73347285
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347286
feature_type: variation
id: rs1448679462
seq_region_name: 17
source: dbSNP
start: 73347286
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347287
feature_type: variation
id: rs2062492797
seq_region_name: 17
source: dbSNP
start: 73347287
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347293
feature_type: variation
id: rs748642301
seq_region_name: 17
source: dbSNP
start: 73347293
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347299
feature_type: variation
id: rs1599469334
seq_region_name: 17
source: dbSNP
start: 73347299
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347301
feature_type: variation
id: rs936757338
seq_region_name: 17
source: dbSNP
start: 73347301
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347302
feature_type: variation
id: rs143099650
seq_region_name: 17
source: dbSNP
start: 73347302
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347307
feature_type: variation
id: rs1322409121
seq_region_name: 17
source: dbSNP
start: 73347307
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347308
feature_type: variation
id: rs539718141
seq_region_name: 17
source: dbSNP
start: 73347308
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347313
feature_type: variation
id: rs772489115
seq_region_name: 17
source: dbSNP
start: 73347313
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347314
feature_type: variation
id: rs2062492963
seq_region_name: 17
source: dbSNP
start: 73347314
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347316
feature_type: variation
id: rs371738272
seq_region_name: 17
source: dbSNP
start: 73347316
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347317
feature_type: variation
id: rs917577083
seq_region_name: 17
source: dbSNP
start: 73347317
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347318
feature_type: variation
id: rs2062493049
seq_region_name: 17
source: dbSNP
start: 73347318
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347319
feature_type: variation
id: rs2062493069
seq_region_name: 17
source: dbSNP
start: 73347319
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347322
feature_type: variation
id: rs1222425403
seq_region_name: 17
source: dbSNP
start: 73347322
strand: 1
-
alleles:
- TG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347323
feature_type: variation
id: rs1447507840
seq_region_name: 17
source: dbSNP
start: 73347322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347324
feature_type: variation
id: rs2062493147
seq_region_name: 17
source: dbSNP
start: 73347324
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347326
feature_type: variation
id: rs1258272177
seq_region_name: 17
source: dbSNP
start: 73347326
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347329
feature_type: variation
id: rs1334802061
seq_region_name: 17
source: dbSNP
start: 73347329
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347331
feature_type: variation
id: rs1469420580
seq_region_name: 17
source: dbSNP
start: 73347331
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347333
feature_type: variation
id: rs1426173096
seq_region_name: 17
source: dbSNP
start: 73347333
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347335
feature_type: variation
id: rs2062493276
seq_region_name: 17
source: dbSNP
start: 73347335
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347339
feature_type: variation
id: rs2062493300
seq_region_name: 17
source: dbSNP
start: 73347339
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347340
feature_type: variation
id: rs1174623504
seq_region_name: 17
source: dbSNP
start: 73347340
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347342
feature_type: variation
id: rs557945941
seq_region_name: 17
source: dbSNP
start: 73347342
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347343
feature_type: variation
id: rs949270856
seq_region_name: 17
source: dbSNP
start: 73347343
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347350
feature_type: variation
id: rs2062493371
seq_region_name: 17
source: dbSNP
start: 73347350
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347351
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347508
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347513
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347513
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73347515
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347515
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347516
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347517
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347525
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347526
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347530
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347537
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347537
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347539
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347545
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347547
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347548
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347549
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347556
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73347557
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347557
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73347558
feature_type: variation
id: rs2062495163
seq_region_name: 17
source: dbSNP
start: 73347558
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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end: 73347560
feature_type: variation
id: rs1281127192
seq_region_name: 17
source: dbSNP
start: 73347560
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347561
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347561
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347562
feature_type: variation
id: rs2062495255
seq_region_name: 17
source: dbSNP
start: 73347562
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs765339028
seq_region_name: 17
source: dbSNP
start: 73347565
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1474198401
seq_region_name: 17
source: dbSNP
start: 73347568
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062495335
seq_region_name: 17
source: dbSNP
start: 73347571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347572
feature_type: variation
id: rs1222832682
seq_region_name: 17
source: dbSNP
start: 73347572
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347576
feature_type: variation
id: rs1193992451
seq_region_name: 17
source: dbSNP
start: 73347576
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347577
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347577
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347579
feature_type: variation
id: rs1248931573
seq_region_name: 17
source: dbSNP
start: 73347579
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347581
feature_type: variation
id: rs1599469594
seq_region_name: 17
source: dbSNP
start: 73347581
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347582
feature_type: variation
id: rs1220667945
seq_region_name: 17
source: dbSNP
start: 73347582
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347586
feature_type: variation
id: rs2062495489
seq_region_name: 17
source: dbSNP
start: 73347586
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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start: 73347802
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347805
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73347810
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347811
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347817
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347819
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73347882
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73347883
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347893
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347898
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73347904
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347905
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347906
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347911
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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end: 73347922
feature_type: variation
id: rs1316966401
seq_region_name: 17
source: dbSNP
start: 73347922
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347924
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062499142
seq_region_name: 17
source: dbSNP
start: 73347927
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs989797773
seq_region_name: 17
source: dbSNP
start: 73347928
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1311406645
seq_region_name: 17
source: dbSNP
start: 73347929
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs141766760
seq_region_name: 17
source: dbSNP
start: 73347936
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347937
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347939
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73347948
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1381029780
seq_region_name: 17
source: dbSNP
start: 73347956
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1296062010
seq_region_name: 17
source: dbSNP
start: 73347956
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145387952
seq_region_name: 17
source: dbSNP
start: 73347957
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1360973004
seq_region_name: 17
source: dbSNP
start: 73347958
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs766197988
seq_region_name: 17
source: dbSNP
start: 73347959
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73347961
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347962
feature_type: variation
id: rs942508129
seq_region_name: 17
source: dbSNP
start: 73347962
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347968
feature_type: variation
id: rs909756285
seq_region_name: 17
source: dbSNP
start: 73347968
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347971
feature_type: variation
id: rs753503903
seq_region_name: 17
source: dbSNP
start: 73347971
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062499498
seq_region_name: 17
source: dbSNP
start: 73347976
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs534109619
seq_region_name: 17
source: dbSNP
start: 73347977
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062499562
seq_region_name: 17
source: dbSNP
start: 73347980
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1356420606
seq_region_name: 17
source: dbSNP
start: 73347984
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599469947
seq_region_name: 17
source: dbSNP
start: 73347985
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347986
feature_type: variation
id: rs901228540
seq_region_name: 17
source: dbSNP
start: 73347986
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062499669
seq_region_name: 17
source: dbSNP
start: 73347993
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599469955
seq_region_name: 17
source: dbSNP
start: 73347997
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73347999
feature_type: variation
id: rs1887071211
seq_region_name: 17
source: dbSNP
start: 73347999
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1193267987
seq_region_name: 17
source: dbSNP
start: 73348001
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348001
feature_type: variation
id: rs1259890586
seq_region_name: 17
source: dbSNP
start: 73348001
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348002
feature_type: variation
id: rs2145388084
seq_region_name: 17
source: dbSNP
start: 73348002
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348003
feature_type: variation
id: rs1488819419
seq_region_name: 17
source: dbSNP
start: 73348003
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348009
feature_type: variation
id: rs2062499795
seq_region_name: 17
source: dbSNP
start: 73348009
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348017
feature_type: variation
id: rs754606101
seq_region_name: 17
source: dbSNP
start: 73348017
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348018
feature_type: variation
id: rs555857878
seq_region_name: 17
source: dbSNP
start: 73348018
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348024
feature_type: variation
id: rs2062499861
seq_region_name: 17
source: dbSNP
start: 73348024
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348026
feature_type: variation
id: rs1265870183
seq_region_name: 17
source: dbSNP
start: 73348026
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348027
feature_type: variation
id: rs1220830916
seq_region_name: 17
source: dbSNP
start: 73348027
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348028
feature_type: variation
id: rs574070167
seq_region_name: 17
source: dbSNP
start: 73348028
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348032
feature_type: variation
id: rs1013973188
seq_region_name: 17
source: dbSNP
start: 73348032
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348033
feature_type: variation
id: rs2062499969
seq_region_name: 17
source: dbSNP
start: 73348033
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348035
feature_type: variation
id: rs1045434354
seq_region_name: 17
source: dbSNP
start: 73348035
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348039
feature_type: variation
id: rs2062500023
seq_region_name: 17
source: dbSNP
start: 73348039
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348040
feature_type: variation
id: rs756182173
seq_region_name: 17
source: dbSNP
start: 73348040
strand: 1
-
alleles:
- CCCAGGACATCCCAGG
- CCCAGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348056
feature_type: variation
id: rs1443083975
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062501174
seq_region_name: 17
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start: 73348162
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73348182
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73348187
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348188
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs374713009
seq_region_name: 17
source: dbSNP
start: 73348189
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73348193
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73348196
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348197
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs977820507
seq_region_name: 17
source: dbSNP
start: 73348199
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348205
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062501529
seq_region_name: 17
source: dbSNP
start: 73348209
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062501556
seq_region_name: 17
source: dbSNP
start: 73348214
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1378640547
seq_region_name: 17
source: dbSNP
start: 73348215
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs561109269
seq_region_name: 17
source: dbSNP
start: 73348220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1438395678
seq_region_name: 17
source: dbSNP
start: 73348226
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1235788775
seq_region_name: 17
source: dbSNP
start: 73348228
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062501703
seq_region_name: 17
source: dbSNP
start: 73348234
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348236
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348238
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs949849436
seq_region_name: 17
source: dbSNP
start: 73348242
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1045466565
seq_region_name: 17
source: dbSNP
start: 73348250
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1198440310
seq_region_name: 17
source: dbSNP
start: 73348257
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs531323971
seq_region_name: 17
source: dbSNP
start: 73348258
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348261
feature_type: variation
id: rs2062501887
seq_region_name: 17
source: dbSNP
start: 73348261
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145388773
seq_region_name: 17
source: dbSNP
start: 73348262
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062501910
seq_region_name: 17
source: dbSNP
start: 73348263
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs957701274
seq_region_name: 17
source: dbSNP
start: 73348264
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348265
feature_type: variation
id: rs1235239471
seq_region_name: 17
source: dbSNP
start: 73348265
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568360108
seq_region_name: 17
source: dbSNP
start: 73348268
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348274
feature_type: variation
id: rs2062502015
seq_region_name: 17
source: dbSNP
start: 73348274
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs902935714
seq_region_name: 17
source: dbSNP
start: 73348275
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348276
feature_type: variation
id: rs998573904
seq_region_name: 17
source: dbSNP
start: 73348276
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348286
feature_type: variation
id: rs747586760
seq_region_name: 17
source: dbSNP
start: 73348286
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348287
feature_type: variation
id: rs1054508401
seq_region_name: 17
source: dbSNP
start: 73348287
strand: 1
-
alleles:
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- CTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348295
feature_type: variation
id: rs2062502147
seq_region_name: 17
source: dbSNP
start: 73348290
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348292
feature_type: variation
id: rs2062502174
seq_region_name: 17
source: dbSNP
start: 73348292
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73348412
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73348413
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348414
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73348431
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73348440
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348443
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348449
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348453
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73348455
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73348457
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73348458
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348459
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348462
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348466
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348468
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348470
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1227791045
seq_region_name: 17
source: dbSNP
start: 73348471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348472
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348476
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348478
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348479
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs976672905
seq_region_name: 17
source: dbSNP
start: 73348481
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs572394907
seq_region_name: 17
source: dbSNP
start: 73348482
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348497
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348498
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348500
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348502
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs982642003
seq_region_name: 17
source: dbSNP
start: 73348507
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565449699
seq_region_name: 17
source: dbSNP
start: 73348509
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348514
feature_type: variation
id: rs998394284
seq_region_name: 17
source: dbSNP
start: 73348514
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1413972816
seq_region_name: 17
source: dbSNP
start: 73348522
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348523
feature_type: variation
id: rs1166629505
seq_region_name: 17
source: dbSNP
start: 73348523
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348524
feature_type: variation
id: rs1029823226
seq_region_name: 17
source: dbSNP
start: 73348524
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348525
feature_type: variation
id: rs2031289868
seq_region_name: 17
source: dbSNP
start: 73348525
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348526
feature_type: variation
id: rs941473585
seq_region_name: 17
source: dbSNP
start: 73348526
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348528
feature_type: variation
id: rs1056162099
seq_region_name: 17
source: dbSNP
start: 73348528
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348529
feature_type: variation
id: rs75637704
seq_region_name: 17
source: dbSNP
start: 73348529
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348530
feature_type: variation
id: rs376913468
seq_region_name: 17
source: dbSNP
start: 73348530
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348532
feature_type: variation
id: rs2062504782
seq_region_name: 17
source: dbSNP
start: 73348532
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348535
feature_type: variation
id: rs1486777260
seq_region_name: 17
source: dbSNP
start: 73348535
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348537
feature_type: variation
id: rs1244881394
seq_region_name: 17
source: dbSNP
start: 73348537
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348538
feature_type: variation
id: rs1004724156
seq_region_name: 17
source: dbSNP
start: 73348538
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348541
feature_type: variation
id: rs1452244645
seq_region_name: 17
source: dbSNP
start: 73348541
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348544
feature_type: variation
id: rs1275142460
seq_region_name: 17
source: dbSNP
start: 73348544
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348546
feature_type: variation
id: rs1477902852
seq_region_name: 17
source: dbSNP
start: 73348546
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348547
feature_type: variation
id: rs1216959455
seq_region_name: 17
source: dbSNP
start: 73348547
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348549
feature_type: variation
id: rs1317552922
seq_region_name: 17
source: dbSNP
start: 73348549
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348550
feature_type: variation
id: rs2145389644
seq_region_name: 17
source: dbSNP
start: 73348550
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348551
feature_type: variation
id: rs1270823222
seq_region_name: 17
source: dbSNP
start: 73348551
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348553
feature_type: variation
id: rs752075822
seq_region_name: 17
source: dbSNP
start: 73348553
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348554
feature_type: variation
id: rs1365979745
seq_region_name: 17
source: dbSNP
start: 73348554
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348557
feature_type: variation
id: rs1188353007
seq_region_name: 17
source: dbSNP
start: 73348557
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348559
feature_type: variation
id: rs1259429128
seq_region_name: 17
source: dbSNP
start: 73348559
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348560
feature_type: variation
id: rs1474012213
seq_region_name: 17
source: dbSNP
start: 73348560
strand: 1
-
alleles:
- CCCTGCCCCCTGC
- CCCTGCCCCCTGCCCCCTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348572
feature_type: variation
id: rs2062505377
seq_region_name: 17
source: dbSNP
start: 73348560
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348563
feature_type: variation
id: rs1186415104
seq_region_name: 17
source: dbSNP
start: 73348563
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348564
feature_type: variation
id: rs755514140
seq_region_name: 17
source: dbSNP
start: 73348564
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348565
feature_type: variation
id: rs781776052
seq_region_name: 17
source: dbSNP
start: 73348565
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348568
feature_type: variation
id: rs747644131
seq_region_name: 17
source: dbSNP
start: 73348568
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348571
feature_type: variation
id: rs1165703258
seq_region_name: 17
source: dbSNP
start: 73348571
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348572
feature_type: variation
id: rs2062505649
seq_region_name: 17
source: dbSNP
start: 73348572
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348582
feature_type: variation
id: rs201960645
seq_region_name: 17
source: dbSNP
start: 73348582
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348584
feature_type: variation
id: rs186354289
seq_region_name: 17
source: dbSNP
start: 73348584
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348585
feature_type: variation
id: rs770580935
seq_region_name: 17
source: dbSNP
start: 73348585
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348588
feature_type: variation
id: rs1399118596
seq_region_name: 17
source: dbSNP
start: 73348588
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348589
feature_type: variation
id: rs201583539
seq_region_name: 17
source: dbSNP
start: 73348589
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348590
feature_type: variation
id: rs774163315
seq_region_name: 17
source: dbSNP
start: 73348590
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73348592
feature_type: variation
id: rs759366008
seq_region_name: 17
source: dbSNP
start: 73348592
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73348593
feature_type: variation
id: rs1286068388
seq_region_name: 17
source: dbSNP
start: 73348593
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: splice_donor_5th_base_variant
end: 73348594
feature_type: variation
id: rs374117631
seq_region_name: 17
source: dbSNP
start: 73348594
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73348595
feature_type: variation
id: rs775473662
seq_region_name: 17
source: dbSNP
start: 73348595
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73348596
feature_type: variation
id: rs1422876139
seq_region_name: 17
source: dbSNP
start: 73348596
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73348598
feature_type: variation
id: rs1327046901
seq_region_name: 17
source: dbSNP
start: 73348598
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73348601
feature_type: variation
id: rs1229671690
seq_region_name: 17
source: dbSNP
start: 73348601
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73348607
feature_type: variation
id: rs761734155
seq_region_name: 17
source: dbSNP
start: 73348607
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348608
feature_type: variation
id: rs200589595
seq_region_name: 17
source: dbSNP
start: 73348608
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348611
feature_type: variation
id: rs1211580234
seq_region_name: 17
source: dbSNP
start: 73348611
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348613
feature_type: variation
id: rs750565580
seq_region_name: 17
source: dbSNP
start: 73348613
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348614
feature_type: variation
id: rs1010657021
seq_region_name: 17
source: dbSNP
start: 73348614
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348617
feature_type: variation
id: rs763270444
seq_region_name: 17
source: dbSNP
start: 73348617
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348619
feature_type: variation
id: rs1261970646
seq_region_name: 17
source: dbSNP
start: 73348619
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348621
feature_type: variation
id: rs2062506462
seq_region_name: 17
source: dbSNP
start: 73348621
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348626
feature_type: variation
id: rs1429974157
seq_region_name: 17
source: dbSNP
start: 73348626
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348628
feature_type: variation
id: rs766752062
seq_region_name: 17
source: dbSNP
start: 73348628
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348629
feature_type: variation
id: rs751953509
seq_region_name: 17
source: dbSNP
start: 73348629
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348630
feature_type: variation
id: rs199591952
seq_region_name: 17
source: dbSNP
start: 73348630
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348631
feature_type: variation
id: rs755518933
seq_region_name: 17
source: dbSNP
start: 73348631
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348632
feature_type: variation
id: rs914292062
seq_region_name: 17
source: dbSNP
start: 73348632
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348637
feature_type: variation
id: rs2062506703
seq_region_name: 17
source: dbSNP
start: 73348637
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348639
feature_type: variation
id: rs1377612875
seq_region_name: 17
source: dbSNP
start: 73348639
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348641
feature_type: variation
id: rs1568360306
seq_region_name: 17
source: dbSNP
start: 73348641
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348642
feature_type: variation
id: rs1464875399
seq_region_name: 17
source: dbSNP
start: 73348642
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73348642
feature_type: variation
id: rs1568360310
seq_region_name: 17
source: dbSNP
start: 73348642
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348649
feature_type: variation
id: rs2062506898
seq_region_name: 17
source: dbSNP
start: 73348649
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73348650
feature_type: variation
id: rs547010993
seq_region_name: 17
source: dbSNP
start: 73348650
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348652
feature_type: variation
id: rs748849786
seq_region_name: 17
source: dbSNP
start: 73348652
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348653
feature_type: variation
id: rs1384197144
seq_region_name: 17
source: dbSNP
start: 73348653
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348659
feature_type: variation
id: rs770585669
seq_region_name: 17
source: dbSNP
start: 73348659
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73348661
feature_type: variation
id: rs753609924
seq_region_name: 17
source: dbSNP
start: 73348661
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348662
feature_type: variation
id: rs371061421
seq_region_name: 17
source: dbSNP
start: 73348662
strand: 1
-
alleles:
- TATTTGGTGA
- TATTTGGTGATATTTGGTGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73348675
feature_type: variation
id: rs2062507191
seq_region_name: 17
source: dbSNP
start: 73348666
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348669
feature_type: variation
id: rs775350970
seq_region_name: 17
source: dbSNP
start: 73348669
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348676
feature_type: variation
id: rs1188519177
seq_region_name: 17
source: dbSNP
start: 73348676
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348681
feature_type: variation
id: rs2062507285
seq_region_name: 17
source: dbSNP
start: 73348681
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348682
feature_type: variation
id: rs867369140
seq_region_name: 17
source: dbSNP
start: 73348682
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73348683
feature_type: variation
id: rs376020251
seq_region_name: 17
source: dbSNP
start: 73348683
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348685
feature_type: variation
id: rs769725413
seq_region_name: 17
source: dbSNP
start: 73348685
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348686
feature_type: variation
id: rs150319493
seq_region_name: 17
source: dbSNP
start: 73348686
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348687
feature_type: variation
id: rs766692489
seq_region_name: 17
source: dbSNP
start: 73348687
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73348689
feature_type: variation
id: rs1246809361
seq_region_name: 17
source: dbSNP
start: 73348689
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73348694
feature_type: variation
id: rs759164295
seq_region_name: 17
source: dbSNP
start: 73348694
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348698
feature_type: variation
id: rs759910725
seq_region_name: 17
source: dbSNP
start: 73348698
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348704
feature_type: variation
id: rs753094584
seq_region_name: 17
source: dbSNP
start: 73348704
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348716
feature_type: variation
id: rs191673430
seq_region_name: 17
source: dbSNP
start: 73348716
strand: 1
-
alleles:
- GGGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73348721
feature_type: variation
id: rs770383131
seq_region_name: 17
source: dbSNP
start: 73348716
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348717
feature_type: variation
id: rs756827895
seq_region_name: 17
source: dbSNP
start: 73348717
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73348719
feature_type: variation
id: rs778470756
seq_region_name: 17
source: dbSNP
start: 73348719
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73348721
feature_type: variation
id: rs2062507797
seq_region_name: 17
source: dbSNP
start: 73348721
strand: 1
-
alleles:
- G
- A
- C
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73348724
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73348737
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs2062508481
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GC
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73348806
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73348810
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73348818
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73348819
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73348822
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73348829
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73348832
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73348838
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73348843
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73348852
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348855
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348860
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348863
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348864
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348870
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73348871
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348873
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73348874
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599470899
seq_region_name: 17
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start: 73348877
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062509494
seq_region_name: 17
source: dbSNP
start: 73348881
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062509519
seq_region_name: 17
source: dbSNP
start: 73348884
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062509548
seq_region_name: 17
source: dbSNP
start: 73348888
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062509572
seq_region_name: 17
source: dbSNP
start: 73348892
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348895
feature_type: variation
id: rs2062509598
seq_region_name: 17
source: dbSNP
start: 73348895
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1029353116
seq_region_name: 17
source: dbSNP
start: 73348902
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1217886878
seq_region_name: 17
source: dbSNP
start: 73348909
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1357064530
seq_region_name: 17
source: dbSNP
start: 73348917
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348922
feature_type: variation
id: rs112257538
seq_region_name: 17
source: dbSNP
start: 73348922
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348925
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348927
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348928
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1290607825
seq_region_name: 17
source: dbSNP
start: 73348938
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348942
feature_type: variation
id: rs1456427009
seq_region_name: 17
source: dbSNP
start: 73348942
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348947
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73348947
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348948
feature_type: variation
id: rs1368031389
seq_region_name: 17
source: dbSNP
start: 73348948
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs962573498
seq_region_name: 17
source: dbSNP
start: 73348951
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348953
feature_type: variation
id: rs1165854938
seq_region_name: 17
source: dbSNP
start: 73348953
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348954
feature_type: variation
id: rs1476312960
seq_region_name: 17
source: dbSNP
start: 73348954
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348955
feature_type: variation
id: rs115539695
seq_region_name: 17
source: dbSNP
start: 73348955
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348956
feature_type: variation
id: rs2062510071
seq_region_name: 17
source: dbSNP
start: 73348956
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348958
feature_type: variation
id: rs2062510093
seq_region_name: 17
source: dbSNP
start: 73348958
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73348962
feature_type: variation
id: rs868525334
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strand: 1
-
alleles:
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-
alleles:
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs759428030
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599471013
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1213850315
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062510606
seq_region_name: 17
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start: 73349009
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349015
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1440788334
seq_region_name: 17
source: dbSNP
start: 73349020
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349023
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs9906579
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs943531556
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1390023410
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1398356046
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1039639149
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349064
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349064
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349072
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349073
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062511378
seq_region_name: 17
source: dbSNP
start: 73349078
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs974491824
seq_region_name: 17
source: dbSNP
start: 73349083
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs540044732
seq_region_name: 17
source: dbSNP
start: 73349084
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349086
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs954393425
seq_region_name: 17
source: dbSNP
start: 73349087
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349089
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145391347
seq_region_name: 17
source: dbSNP
start: 73349093
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062511603
seq_region_name: 17
source: dbSNP
start: 73349094
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062511629
seq_region_name: 17
source: dbSNP
start: 73349099
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1252860547
seq_region_name: 17
source: dbSNP
start: 73349113
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs79032809
seq_region_name: 17
source: dbSNP
start: 73349114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs780135423
seq_region_name: 17
source: dbSNP
start: 73349115
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062511758
seq_region_name: 17
source: dbSNP
start: 73349117
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599471127
seq_region_name: 17
source: dbSNP
start: 73349121
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062511822
seq_region_name: 17
source: dbSNP
start: 73349124
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1330472519
seq_region_name: 17
source: dbSNP
start: 73349125
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349126
feature_type: variation
id: rs2062511883
seq_region_name: 17
source: dbSNP
start: 73349126
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349128
feature_type: variation
id: rs1599471131
seq_region_name: 17
source: dbSNP
start: 73349128
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs79134486
seq_region_name: 17
source: dbSNP
start: 73349129
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349130
feature_type: variation
id: rs768697217
seq_region_name: 17
source: dbSNP
start: 73349130
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349131
feature_type: variation
id: rs1330920719
seq_region_name: 17
source: dbSNP
start: 73349131
strand: 1
-
alleles:
- TGTGAAATGCCCCCTTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349148
feature_type: variation
id: rs1374856217
seq_region_name: 17
source: dbSNP
start: 73349131
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1038996075
seq_region_name: 17
source: dbSNP
start: 73349138
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349140
feature_type: variation
id: rs112903842
seq_region_name: 17
source: dbSNP
start: 73349140
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062512100
seq_region_name: 17
source: dbSNP
start: 73349141
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349146
feature_type: variation
id: rs948852211
seq_region_name: 17
source: dbSNP
start: 73349146
strand: 1
-
alleles:
- TTAC
- TTACTTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349151
feature_type: variation
id: rs2062512181
seq_region_name: 17
source: dbSNP
start: 73349148
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349153
feature_type: variation
id: rs187161309
seq_region_name: 17
source: dbSNP
start: 73349153
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349154
feature_type: variation
id: rs1196099427
seq_region_name: 17
source: dbSNP
start: 73349154
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349155
feature_type: variation
id: rs1455189089
seq_region_name: 17
source: dbSNP
start: 73349155
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349156
feature_type: variation
id: rs2145391525
seq_region_name: 17
source: dbSNP
start: 73349156
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349157
feature_type: variation
id: rs907291089
seq_region_name: 17
source: dbSNP
start: 73349157
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349158
feature_type: variation
id: rs9302961
seq_region_name: 17
source: dbSNP
start: 73349158
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349158
feature_type: variation
id: rs752618041
seq_region_name: 17
source: dbSNP
start: 73349158
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349159
feature_type: variation
id: rs760639722
seq_region_name: 17
source: dbSNP
start: 73349159
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349160
feature_type: variation
id: rs1242848898
seq_region_name: 17
source: dbSNP
start: 73349160
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349166
feature_type: variation
id: rs1344090205
seq_region_name: 17
source: dbSNP
start: 73349166
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349167
feature_type: variation
id: rs956038982
seq_region_name: 17
source: dbSNP
start: 73349167
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349176
feature_type: variation
id: rs1011505392
seq_region_name: 17
source: dbSNP
start: 73349176
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349177
feature_type: variation
id: rs2062512605
seq_region_name: 17
source: dbSNP
start: 73349177
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349180
feature_type: variation
id: rs571837243
seq_region_name: 17
source: dbSNP
start: 73349180
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349181
feature_type: variation
id: rs1249101688
seq_region_name: 17
source: dbSNP
start: 73349181
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349184
feature_type: variation
id: rs2062512720
seq_region_name: 17
source: dbSNP
start: 73349181
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349182
feature_type: variation
id: rs2062512744
seq_region_name: 17
source: dbSNP
start: 73349182
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349185
feature_type: variation
id: rs914816900
seq_region_name: 17
source: dbSNP
start: 73349185
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349186
feature_type: variation
id: rs2062512812
seq_region_name: 17
source: dbSNP
start: 73349186
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349187
feature_type: variation
id: rs900344042
seq_region_name: 17
source: dbSNP
start: 73349187
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349190
feature_type: variation
id: rs1418552392
seq_region_name: 17
source: dbSNP
start: 73349190
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349191
feature_type: variation
id: rs2062512908
seq_region_name: 17
source: dbSNP
start: 73349191
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349194
feature_type: variation
id: rs1177197405
seq_region_name: 17
source: dbSNP
start: 73349194
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349196
feature_type: variation
id: rs2062512969
seq_region_name: 17
source: dbSNP
start: 73349196
strand: 1
-
alleles:
- GCTGGGCCTGGCTGGGCCTG
- GCTGGGCCTG
- GCTGGGCCTGGCTGGGCCTGGCTGGGCCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349217
feature_type: variation
id: rs1259329340
seq_region_name: 17
source: dbSNP
start: 73349198
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349203
feature_type: variation
id: rs2062513027
seq_region_name: 17
source: dbSNP
start: 73349203
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349207
feature_type: variation
id: rs2062513056
seq_region_name: 17
source: dbSNP
start: 73349207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349209
feature_type: variation
id: rs2062513090
seq_region_name: 17
source: dbSNP
start: 73349209
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349213
feature_type: variation
id: rs2062513115
seq_region_name: 17
source: dbSNP
start: 73349213
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349217
feature_type: variation
id: rs2062513140
seq_region_name: 17
source: dbSNP
start: 73349217
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349220
feature_type: variation
id: rs2062513169
seq_region_name: 17
source: dbSNP
start: 73349220
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349224
feature_type: variation
id: rs943636547
seq_region_name: 17
source: dbSNP
start: 73349224
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349226
feature_type: variation
id: rs1030124907
seq_region_name: 17
source: dbSNP
start: 73349226
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349232
feature_type: variation
id: rs1431573582
seq_region_name: 17
source: dbSNP
start: 73349232
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349234
feature_type: variation
id: rs2062513306
seq_region_name: 17
source: dbSNP
start: 73349234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349237
feature_type: variation
id: rs2145391757
seq_region_name: 17
source: dbSNP
start: 73349237
strand: 1
-
alleles:
- CTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349240
feature_type: variation
id: rs2062513332
seq_region_name: 17
source: dbSNP
start: 73349237
strand: 1
-
alleles:
- TCTTTCTTT
- TCTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349246
feature_type: variation
id: rs1468374261
seq_region_name: 17
source: dbSNP
start: 73349238
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349240
feature_type: variation
id: rs539145727
seq_region_name: 17
source: dbSNP
start: 73349240
strand: 1
-
alleles:
- TTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349242
feature_type: variation
id: rs2062513401
seq_region_name: 17
source: dbSNP
start: 73349240
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349243
feature_type: variation
id: rs2145391790
seq_region_name: 17
source: dbSNP
start: 73349243
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349246
feature_type: variation
id: rs2062513429
seq_region_name: 17
source: dbSNP
start: 73349246
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349247
feature_type: variation
id: rs2062513455
seq_region_name: 17
source: dbSNP
start: 73349247
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349250
feature_type: variation
id: rs1365153737
seq_region_name: 17
source: dbSNP
start: 73349250
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349252
feature_type: variation
id: rs2062513508
seq_region_name: 17
source: dbSNP
start: 73349252
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349257
feature_type: variation
id: rs1185051723
seq_region_name: 17
source: dbSNP
start: 73349257
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349261
feature_type: variation
id: rs1485216498
seq_region_name: 17
source: dbSNP
start: 73349261
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349264
feature_type: variation
id: rs1257985800
seq_region_name: 17
source: dbSNP
start: 73349264
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349267
feature_type: variation
id: rs983549674
seq_region_name: 17
source: dbSNP
start: 73349267
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349268
feature_type: variation
id: rs547283439
seq_region_name: 17
source: dbSNP
start: 73349268
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349269
feature_type: variation
id: rs1400748034
seq_region_name: 17
source: dbSNP
start: 73349269
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349270
feature_type: variation
id: rs1014603316
seq_region_name: 17
source: dbSNP
start: 73349270
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349272
feature_type: variation
id: rs2062513752
seq_region_name: 17
source: dbSNP
start: 73349272
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349273
feature_type: variation
id: rs760563641
seq_region_name: 17
source: dbSNP
start: 73349273
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349274
feature_type: variation
id: rs1296358813
seq_region_name: 17
source: dbSNP
start: 73349274
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349275
feature_type: variation
id: rs2062513852
seq_region_name: 17
source: dbSNP
start: 73349275
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349278
feature_type: variation
id: rs933509247
seq_region_name: 17
source: dbSNP
start: 73349278
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349279
feature_type: variation
id: rs1282637141
seq_region_name: 17
source: dbSNP
start: 73349279
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349280
feature_type: variation
id: rs1050827133
seq_region_name: 17
source: dbSNP
start: 73349280
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349285
feature_type: variation
id: rs1244409983
seq_region_name: 17
source: dbSNP
start: 73349285
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349286
feature_type: variation
id: rs1356433874
seq_region_name: 17
source: dbSNP
start: 73349286
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349287
feature_type: variation
id: rs2062514032
seq_region_name: 17
source: dbSNP
start: 73349287
strand: 1
-
alleles:
- GAGCTCCTCCCTCCATCCTCTAGATGAACACACACATAGCTTCGTCCCTCTAAGACAGAGACAGAGGGAAGCTTTGTGAGCTCCT
- GAGCTCCTCCCTCCATCCTCTAGATGAACACACACATAGCTTCGTCCCTCTAAGACAGAGACAGAGGGAAGCTTTGTGAGCTCCTCCCTCCATCCTCTAGATGAACACACACATAGCTTCGTCCCTCTAAGACAGAGACAGAGGGAAGCTTTGTGAGCTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349371
feature_type: variation
id: rs2062514063
seq_region_name: 17
source: dbSNP
start: 73349287
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349292
feature_type: variation
id: rs2062514097
seq_region_name: 17
source: dbSNP
start: 73349292
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349293
feature_type: variation
id: rs2145391943
seq_region_name: 17
source: dbSNP
start: 73349293
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349295
feature_type: variation
id: rs886879213
seq_region_name: 17
source: dbSNP
start: 73349295
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349298
feature_type: variation
id: rs2062514150
seq_region_name: 17
source: dbSNP
start: 73349298
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349299
feature_type: variation
id: rs1284589721
seq_region_name: 17
source: dbSNP
start: 73349299
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349300
feature_type: variation
id: rs2145391965
seq_region_name: 17
source: dbSNP
start: 73349300
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349303
feature_type: variation
id: rs2062514218
seq_region_name: 17
source: dbSNP
start: 73349303
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349308
feature_type: variation
id: rs2062514249
seq_region_name: 17
source: dbSNP
start: 73349308
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349310
feature_type: variation
id: rs190947991
seq_region_name: 17
source: dbSNP
start: 73349310
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349311
feature_type: variation
id: rs1222520511
seq_region_name: 17
source: dbSNP
start: 73349311
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349314
feature_type: variation
id: rs2062514334
seq_region_name: 17
source: dbSNP
start: 73349314
strand: 1
-
alleles:
- ACACACACA
- ACACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349322
feature_type: variation
id: rs1319603136
seq_region_name: 17
source: dbSNP
start: 73349314
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349319
feature_type: variation
id: rs1400782517
seq_region_name: 17
source: dbSNP
start: 73349319
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349327
feature_type: variation
id: rs2062514412
seq_region_name: 17
source: dbSNP
start: 73349327
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349330
feature_type: variation
id: rs1038455416
seq_region_name: 17
source: dbSNP
start: 73349330
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349331
feature_type: variation
id: rs1193853422
seq_region_name: 17
source: dbSNP
start: 73349331
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349332
feature_type: variation
id: rs770862322
seq_region_name: 17
source: dbSNP
start: 73349332
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349333
feature_type: variation
id: rs1013254911
seq_region_name: 17
source: dbSNP
start: 73349333
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349336
feature_type: variation
id: rs2062514555
seq_region_name: 17
source: dbSNP
start: 73349336
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349340
feature_type: variation
id: rs2062514589
seq_region_name: 17
source: dbSNP
start: 73349340
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349344
feature_type: variation
id: rs566127968
seq_region_name: 17
source: dbSNP
start: 73349344
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349348
feature_type: variation
id: rs776431955
seq_region_name: 17
source: dbSNP
start: 73349348
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349352
feature_type: variation
id: rs907039202
seq_region_name: 17
source: dbSNP
start: 73349352
strand: 1
-
alleles:
- AGCTTTGTGAGCT
- AGCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349368
feature_type: variation
id: rs1189820961
seq_region_name: 17
source: dbSNP
start: 73349356
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349358
feature_type: variation
id: rs1207119486
seq_region_name: 17
source: dbSNP
start: 73349358
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349363
feature_type: variation
id: rs2062514790
seq_region_name: 17
source: dbSNP
start: 73349363
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349366
feature_type: variation
id: rs980238791
seq_region_name: 17
source: dbSNP
start: 73349366
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349367
feature_type: variation
id: rs2062514814
seq_region_name: 17
source: dbSNP
start: 73349367
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349371
feature_type: variation
id: rs2145392115
seq_region_name: 17
source: dbSNP
start: 73349371
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349372
feature_type: variation
id: rs2062514852
seq_region_name: 17
source: dbSNP
start: 73349372
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349374
feature_type: variation
id: rs1216492140
seq_region_name: 17
source: dbSNP
start: 73349374
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349376
feature_type: variation
id: rs2062514903
seq_region_name: 17
source: dbSNP
start: 73349376
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349377
feature_type: variation
id: rs2062514939
seq_region_name: 17
source: dbSNP
start: 73349377
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349384
feature_type: variation
id: rs1599471387
seq_region_name: 17
source: dbSNP
start: 73349384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349385
feature_type: variation
id: rs1002701356
seq_region_name: 17
source: dbSNP
start: 73349385
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349386
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73349503
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349508
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349517
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349521
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349522
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349530
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349534
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349538
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349540
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349545
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349548
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349549
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349550
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349552
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73349557
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349558
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349559
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349560
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349562
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs939786113
seq_region_name: 17
source: dbSNP
start: 73349568
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73349570
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1038003555
seq_region_name: 17
source: dbSNP
start: 73349572
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599471563
seq_region_name: 17
source: dbSNP
start: 73349573
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349574
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1343082004
seq_region_name: 17
source: dbSNP
start: 73349575
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349577
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349585
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349589
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs919594976
seq_region_name: 17
source: dbSNP
start: 73349593
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349594
feature_type: variation
id: rs2062516761
seq_region_name: 17
source: dbSNP
start: 73349594
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062516796
seq_region_name: 17
source: dbSNP
start: 73349599
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1278408527
seq_region_name: 17
source: dbSNP
start: 73349603
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1170911472
seq_region_name: 17
source: dbSNP
start: 73349607
strand: 1
-
alleles:
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- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145392611
seq_region_name: 17
source: dbSNP
start: 73349614
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599471586
seq_region_name: 17
source: dbSNP
start: 73349620
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349624
feature_type: variation
id: rs2062516899
seq_region_name: 17
source: dbSNP
start: 73349624
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349625
feature_type: variation
id: rs948449609
seq_region_name: 17
source: dbSNP
start: 73349625
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349629
feature_type: variation
id: rs2062516959
seq_region_name: 17
source: dbSNP
start: 73349629
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73349632
feature_type: variation
id: rs1030154661
seq_region_name: 17
source: dbSNP
start: 73349632
strand: 1
-
alleles:
- GC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349633
feature_type: variation
id: rs1363590438
seq_region_name: 17
source: dbSNP
start: 73349632
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349633
feature_type: variation
id: rs183529569
seq_region_name: 17
source: dbSNP
start: 73349633
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349634
feature_type: variation
id: rs4969106
seq_region_name: 17
source: dbSNP
start: 73349634
strand: 1
-
alleles:
- C
- CGAGCCTTGTCCTGTCCTCGCGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349635
feature_type: variation
id: rs1568360707
seq_region_name: 17
source: dbSNP
start: 73349635
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349635
feature_type: variation
id: rs2062517145
seq_region_name: 17
source: dbSNP
start: 73349635
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349638
feature_type: variation
id: rs751148051
seq_region_name: 17
source: dbSNP
start: 73349638
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349639
feature_type: variation
id: rs2062517215
seq_region_name: 17
source: dbSNP
start: 73349639
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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alleles:
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73349713
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062517680
seq_region_name: 17
source: dbSNP
start: 73349715
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs541790057
seq_region_name: 17
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start: 73349717
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349729
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73349730
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73349735
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73349740
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73349778
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349780
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349788
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1284567183
seq_region_name: 17
source: dbSNP
start: 73349789
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349794
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349798
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349800
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349801
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1353262816
seq_region_name: 17
source: dbSNP
start: 73349807
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349808
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349812
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349817
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062518528
seq_region_name: 17
source: dbSNP
start: 73349817
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062518567
seq_region_name: 17
source: dbSNP
start: 73349823
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349825
feature_type: variation
id: rs1247230030
seq_region_name: 17
source: dbSNP
start: 73349825
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs565482594
seq_region_name: 17
source: dbSNP
start: 73349826
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349831
feature_type: variation
id: rs974224020
seq_region_name: 17
source: dbSNP
start: 73349831
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs756402691
seq_region_name: 17
source: dbSNP
start: 73349832
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349833
feature_type: variation
id: rs1284976690
seq_region_name: 17
source: dbSNP
start: 73349833
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349837
feature_type: variation
id: rs1161481115
seq_region_name: 17
source: dbSNP
start: 73349837
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062518782
seq_region_name: 17
source: dbSNP
start: 73349839
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349840
feature_type: variation
id: rs532751978
seq_region_name: 17
source: dbSNP
start: 73349840
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349841
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349841
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1422289501
seq_region_name: 17
source: dbSNP
start: 73349843
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs780513016
seq_region_name: 17
source: dbSNP
start: 73349845
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349848
feature_type: variation
id: rs1189122215
seq_region_name: 17
source: dbSNP
start: 73349848
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349851
feature_type: variation
id: rs948373257
seq_region_name: 17
source: dbSNP
start: 73349851
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349852
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349852
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349863
feature_type: variation
id: rs1261651215
seq_region_name: 17
source: dbSNP
start: 73349863
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349868
feature_type: variation
id: rs1044070943
seq_region_name: 17
source: dbSNP
start: 73349868
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349869
feature_type: variation
id: rs529772475
seq_region_name: 17
source: dbSNP
start: 73349869
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349874
feature_type: variation
id: rs2062519019
seq_region_name: 17
source: dbSNP
start: 73349874
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349876
feature_type: variation
id: rs2062519045
seq_region_name: 17
source: dbSNP
start: 73349876
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349879
feature_type: variation
id: rs1260810245
seq_region_name: 17
source: dbSNP
start: 73349879
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062519066
seq_region_name: 17
source: dbSNP
start: 73349883
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349887
feature_type: variation
id: rs1599471853
seq_region_name: 17
source: dbSNP
start: 73349887
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73349888
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349889
feature_type: variation
id: rs2062519131
seq_region_name: 17
source: dbSNP
start: 73349889
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349899
feature_type: variation
id: rs151113350
seq_region_name: 17
source: dbSNP
start: 73349899
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349902
feature_type: variation
id: rs749460499
seq_region_name: 17
source: dbSNP
start: 73349902
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349903
feature_type: variation
id: rs2062519225
seq_region_name: 17
source: dbSNP
start: 73349903
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349904
feature_type: variation
id: rs2062519254
seq_region_name: 17
source: dbSNP
start: 73349904
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349906
feature_type: variation
id: rs768893812
seq_region_name: 17
source: dbSNP
start: 73349906
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73349909
feature_type: variation
id: rs891614809
seq_region_name: 17
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start: 73349909
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350146
feature_type: variation
id: rs1599472109
seq_region_name: 17
source: dbSNP
start: 73350146
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350148
feature_type: variation
id: rs1044770737
seq_region_name: 17
source: dbSNP
start: 73350148
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350153
feature_type: variation
id: rs2062521710
seq_region_name: 17
source: dbSNP
start: 73350153
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350155
feature_type: variation
id: rs2062521732
seq_region_name: 17
source: dbSNP
start: 73350155
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350159
feature_type: variation
id: rs2062521753
seq_region_name: 17
source: dbSNP
start: 73350159
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350160
feature_type: variation
id: rs1568360888
seq_region_name: 17
source: dbSNP
start: 73350160
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350164
feature_type: variation
id: rs988686260
seq_region_name: 17
source: dbSNP
start: 73350164
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350167
feature_type: variation
id: rs2062521874
seq_region_name: 17
source: dbSNP
start: 73350167
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350168
feature_type: variation
id: rs1003154467
seq_region_name: 17
source: dbSNP
start: 73350168
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350170
feature_type: variation
id: rs2062521922
seq_region_name: 17
source: dbSNP
start: 73350170
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350173
feature_type: variation
id: rs2062521955
seq_region_name: 17
source: dbSNP
start: 73350173
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350175
feature_type: variation
id: rs2062521996
seq_region_name: 17
source: dbSNP
start: 73350175
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350179
feature_type: variation
id: rs1283692507
seq_region_name: 17
source: dbSNP
start: 73350179
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350181
feature_type: variation
id: rs1347160017
seq_region_name: 17
source: dbSNP
start: 73350181
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350182
feature_type: variation
id: rs1599472129
seq_region_name: 17
source: dbSNP
start: 73350182
strand: 1
-
alleles:
- CCCCACCTGGGCACTGCTGGGCCTGGCCCCC
- CCCCACCTGGGCACTGCTGGGCCTGGCCCCCCACCTGGGCACTGCTGGGCCTGGCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs1304300307
seq_region_name: 17
source: dbSNP
start: 73350183
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350184
feature_type: variation
id: rs1236715480
seq_region_name: 17
source: dbSNP
start: 73350184
strand: 1
-
alleles:
- "-"
- TCTGGGCACTGCTGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350187
feature_type: variation
id: rs2062522234
seq_region_name: 17
source: dbSNP
start: 73350188
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350189
feature_type: variation
id: rs759857459
seq_region_name: 17
source: dbSNP
start: 73350189
strand: 1
-
alleles:
- C
- CCGGGCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350189
feature_type: variation
id: rs771236746
seq_region_name: 17
source: dbSNP
start: 73350189
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350190
feature_type: variation
id: rs62071382
seq_region_name: 17
source: dbSNP
start: 73350190
strand: 1
-
alleles:
- G
- GCTGGGCCTGGCCCCCCACCCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350191
feature_type: variation
id: rs2062522379
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GG
- GGCCCCCCACCCGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350192
feature_type: variation
id: rs2062522409
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGG
- GGGGCACTGCTGGGCCTGGCCCCCCACCCGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350193
feature_type: variation
id: rs147120981
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGC
- GGGCCCTGCTGGGCCTGGCCCCCCACCCGGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350194
feature_type: variation
id: rs2145393939
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGCA
- GGGCAGTGCTGGGCCTGGCCCCCCACCCGGGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350195
feature_type: variation
id: rs2062522454
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGCACTGC
- GGGCACTGCCGGGCCTGGCCCCCCACCCGGGCACTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350199
feature_type: variation
id: rs1568360911
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGCACTGCTGGG
- GGGCACTGCTGGGACTGGCCCCCCACCCGGGCACTGCTGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350203
feature_type: variation
id: rs2062522504
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGCACTGCTGGGC
- GGGCACTGCTGGGCTTGGCCCCCCACCCGGGCACTGCTGGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350204
feature_type: variation
id: rs2062522539
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGCACTGCTGGGCCTGGC
- GGGCACTGCTGGGCCTGGCTCCCCACCCGGGCACTGCTGGGCCTGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350209
feature_type: variation
id: rs2062522566
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GGGCACTGCTGGGCCTGGCCCCC
- GGGCACTGCTGGGCCTGGCCCCCCACCCGGGCACTGCTGGGCCTGGCCCCC
- GGGCACTGCTGGGCCTGGCCCCCCATCCGGGCACTGCTGGGCCTGGCCCCC
- GGGCACTGCTGGGCCTGGCCCCCCGGGCACTGCTGGGCCTGGCCCCC
- GGGCACTGCTGGGCCTGGCCCCCGACCCGGGCACTGCTGGGCCTGGCCCCC
- GGGCACTGCTGGGCCTGGCCCCCTACCCGGGCACTGCTGGGCCTGGCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs149822544
seq_region_name: 17
source: dbSNP
start: 73350191
strand: 1
-
alleles:
- GG
- GGGCACTGCTGGGCCTGGCCCCCCACCCGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350193
feature_type: variation
id: rs1555749317
seq_region_name: 17
source: dbSNP
start: 73350192
strand: 1
-
alleles:
- GGCACTGCTGGGCCTGGCCCCC
- GGCACTGCTGGGCCTGGCCCCCCACCCAGGCACTGCTGGGCCTGGCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs2062522674
seq_region_name: 17
source: dbSNP
start: 73350192
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350196
feature_type: variation
id: rs767953091
seq_region_name: 17
source: dbSNP
start: 73350196
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350199
feature_type: variation
id: rs2062522710
seq_region_name: 17
source: dbSNP
start: 73350199
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350200
feature_type: variation
id: rs775891133
seq_region_name: 17
source: dbSNP
start: 73350200
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350201
feature_type: variation
id: rs1435596701
seq_region_name: 17
source: dbSNP
start: 73350201
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350205
feature_type: variation
id: rs760994064
seq_region_name: 17
source: dbSNP
start: 73350205
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350206
feature_type: variation
id: rs764649017
seq_region_name: 17
source: dbSNP
start: 73350206
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350208
feature_type: variation
id: rs1298714158
seq_region_name: 17
source: dbSNP
start: 73350207
strand: 1
-
alleles:
- "-"
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350208
feature_type: variation
id: rs1555749326
seq_region_name: 17
source: dbSNP
start: 73350209
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350209
feature_type: variation
id: rs1375196325
seq_region_name: 17
source: dbSNP
start: 73350209
strand: 1
-
alleles:
- CCCCC
- CCCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs774573777
seq_region_name: 17
source: dbSNP
start: 73350209
strand: 1
-
alleles:
- "-"
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350209
feature_type: variation
id: rs760646905
seq_region_name: 17
source: dbSNP
start: 73350210
strand: 1
-
alleles:
- CCCC
- CCCCCACCCGGGCACTGCTGGGCCTGGTCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs2062522961
seq_region_name: 17
source: dbSNP
start: 73350210
strand: 1
-
alleles:
- "-"
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350210
feature_type: variation
id: rs764130031
seq_region_name: 17
source: dbSNP
start: 73350211
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350211
feature_type: variation
id: rs1311529331
seq_region_name: 17
source: dbSNP
start: 73350211
strand: 1
-
alleles:
- "-"
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350211
feature_type: variation
id: rs761719987
seq_region_name: 17
source: dbSNP
start: 73350212
strand: 1
-
alleles:
- CC
- CCCACCCGGGCACTGCTGGGCCTGGCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs2062523065
seq_region_name: 17
source: dbSNP
start: 73350212
strand: 1
-
alleles:
- "-"
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350212
feature_type: variation
id: rs750105039
seq_region_name: 17
source: dbSNP
start: 73350213
strand: 1
-
alleles:
- C
- CCACCCGGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs1555749331
seq_region_name: 17
source: dbSNP
start: 73350213
strand: 1
-
alleles:
- "-"
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350213
feature_type: variation
id: rs375803616
seq_region_name: 17
source: dbSNP
start: 73350214
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350214
feature_type: variation
id: rs9748160
seq_region_name: 17
source: dbSNP
start: 73350214
strand: 1
-
alleles:
- A
- CACCCGGGCACTGCTGGGCCTGGCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350214
feature_type: variation
id: rs1555749343
seq_region_name: 17
source: dbSNP
start: 73350214
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350215
feature_type: variation
id: rs869082711
seq_region_name: 17
source: dbSNP
start: 73350214
strand: 1
-
alleles:
- "-"
- CCCAGGCACTGCTGGGCCTGGCCCCCC
- CCCGGGCACGGCTGGGCCTGGCCCCCC
- CCCGGGCACTACTGGGCCTGGCCCCCC
- CCCGGGCACTGCCGGGCCTGGCCCCCC
- CCCGGGCACTGCTGGGCCTGGCCCCC
- CCCGGGCACTGCTGGGCCTGGCCCCCC
- CCCGGGCACTGCTGGGCCTGGCCCCCCACCCGGGCACTGCTGGGCCTGGCCCCCC
- CCCGGGCACTGCTGGGCCTGGCCTCCC
- CCCGGGCACTGCTGGGCCTGGTCCCCC
- CCTGGGCACTGCTGGGCCTGGCCCCCC
- CTGCTGGGCCTGGCCCCCC
- TCCGGGCACTGCTGGGCCTGGCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350214
feature_type: variation
id: rs61494348
seq_region_name: 17
source: dbSNP
start: 73350215
strand: 1
-
alleles:
- ACCC
- ACCCGGGCACTGCTGGGCCTGGCCCCCCACCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350218
feature_type: variation
id: rs2062523377
seq_region_name: 17
source: dbSNP
start: 73350215
strand: 1
-
alleles:
- "-"
- TGGGGGGCCAGGCCCAGCAGTGCCGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350215
feature_type: variation
id: rs1555749349
seq_region_name: 17
source: dbSNP
start: 73350216
strand: 1
-
alleles:
- CCC
- CCCGGGCACTGCTGGGCCTGGCCCCCC
- CCCGGGCACTGCTGGGCCTGGCCCCCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350218
feature_type: variation
id: rs754407828
seq_region_name: 17
source: dbSNP
start: 73350216
strand: 1
-
alleles:
- C
- CGGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350218
feature_type: variation
id: rs370418227
seq_region_name: 17
source: dbSNP
start: 73350218
strand: 1
-
alleles:
- "-"
- GGGCACTGCTGG
- GGGCACTGCTGGGCCTGGCCCCCCACCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350218
feature_type: variation
id: rs370472124
seq_region_name: 17
source: dbSNP
start: 73350219
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350219
feature_type: variation
id: rs754307392
seq_region_name: 17
source: dbSNP
start: 73350219
strand: 1
-
alleles:
- ACGCAGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350225
feature_type: variation
id: rs749740859
seq_region_name: 17
source: dbSNP
start: 73350219
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350220
feature_type: variation
id: rs756699553
seq_region_name: 17
source: dbSNP
start: 73350220
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350220
feature_type: variation
id: rs779319498
seq_region_name: 17
source: dbSNP
start: 73350221
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350221
feature_type: variation
id: rs375027080
seq_region_name: 17
source: dbSNP
start: 73350221
strand: 1
-
alleles:
- "-"
- TGGGCCTGGCCCCCCACCCACAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350222
feature_type: variation
id: rs772383473
seq_region_name: 17
source: dbSNP
start: 73350223
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350223
feature_type: variation
id: rs758017688
seq_region_name: 17
source: dbSNP
start: 73350223
strand: 1
-
alleles:
- AGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350226
feature_type: variation
id: rs1491132060
seq_region_name: 17
source: dbSNP
start: 73350223
strand: 1
-
alleles:
- "-"
- CTGCTGG
- CTGCTGGGCCT
- CTGCTGGGCCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350223
feature_type: variation
id: rs746208643
seq_region_name: 17
source: dbSNP
start: 73350224
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350224
feature_type: variation
id: rs900559101
seq_region_name: 17
source: dbSNP
start: 73350224
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350225
feature_type: variation
id: rs779624996
seq_region_name: 17
source: dbSNP
start: 73350225
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350226
feature_type: variation
id: rs2062523805
seq_region_name: 17
source: dbSNP
start: 73350226
strand: 1
-
alleles:
- "-"
- CCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350226
feature_type: variation
id: rs776722908
seq_region_name: 17
source: dbSNP
start: 73350227
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350229
feature_type: variation
id: rs1252428087
seq_region_name: 17
source: dbSNP
start: 73350229
strand: 1
-
alleles:
- CCC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73350231
feature_type: variation
id: rs761775372
seq_region_name: 17
source: dbSNP
start: 73350229
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350230
feature_type: variation
id: rs754800221
seq_region_name: 17
source: dbSNP
start: 73350230
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73350231
feature_type: variation
id: rs1180467208
seq_region_name: 17
source: dbSNP
start: 73350231
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73350232
feature_type: variation
id: rs200095133
seq_region_name: 17
source: dbSNP
start: 73350232
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73350233
feature_type: variation
id: rs748106343
seq_region_name: 17
source: dbSNP
start: 73350233
strand: 1
-
alleles:
- GTAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73350236
feature_type: variation
id: rs765259732
seq_region_name: 17
source: dbSNP
start: 73350233
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73350234
feature_type: variation
id: rs771082663
seq_region_name: 17
source: dbSNP
start: 73350234
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350238
feature_type: variation
id: rs1183825597
seq_region_name: 17
source: dbSNP
start: 73350238
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350239
feature_type: variation
id: rs1411674916
seq_region_name: 17
source: dbSNP
start: 73350239
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350240
feature_type: variation
id: rs774602104
seq_region_name: 17
source: dbSNP
start: 73350240
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350241
feature_type: variation
id: rs2145394367
seq_region_name: 17
source: dbSNP
start: 73350241
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350242
feature_type: variation
id: rs541528366
seq_region_name: 17
source: dbSNP
start: 73350242
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350243
feature_type: variation
id: rs2145394381
seq_region_name: 17
source: dbSNP
start: 73350243
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350245
feature_type: variation
id: rs775632022
seq_region_name: 17
source: dbSNP
start: 73350245
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350246
feature_type: variation
id: rs2062524237
seq_region_name: 17
source: dbSNP
start: 73350246
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350247
feature_type: variation
id: rs2062524261
seq_region_name: 17
source: dbSNP
start: 73350247
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350250
feature_type: variation
id: rs761034315
seq_region_name: 17
source: dbSNP
start: 73350250
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350251
feature_type: variation
id: rs768917020
seq_region_name: 17
source: dbSNP
start: 73350251
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350252
feature_type: variation
id: rs2145394437
seq_region_name: 17
source: dbSNP
start: 73350252
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350254
feature_type: variation
id: rs777149158
seq_region_name: 17
source: dbSNP
start: 73350254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350258
feature_type: variation
id: rs762340608
seq_region_name: 17
source: dbSNP
start: 73350258
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73350259
feature_type: variation
id: rs765775983
seq_region_name: 17
source: dbSNP
start: 73350259
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350263
feature_type: variation
id: rs1281017951
seq_region_name: 17
source: dbSNP
start: 73350263
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350264
feature_type: variation
id: rs749916035
seq_region_name: 17
source: dbSNP
start: 73350264
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350265
feature_type: variation
id: rs1377747800
seq_region_name: 17
source: dbSNP
start: 73350265
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350269
feature_type: variation
id: rs2062524571
seq_region_name: 17
source: dbSNP
start: 73350269
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350270
feature_type: variation
id: rs1599472411
seq_region_name: 17
source: dbSNP
start: 73350270
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350275
feature_type: variation
id: rs2062524629
seq_region_name: 17
source: dbSNP
start: 73350275
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350277
feature_type: variation
id: rs375316369
seq_region_name: 17
source: dbSNP
start: 73350277
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73350278
feature_type: variation
id: rs138003419
seq_region_name: 17
source: dbSNP
start: 73350278
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350280
feature_type: variation
id: rs2062524726
seq_region_name: 17
source: dbSNP
start: 73350280
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350283
feature_type: variation
id: rs1041851047
seq_region_name: 17
source: dbSNP
start: 73350283
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350285
feature_type: variation
id: rs143527749
seq_region_name: 17
source: dbSNP
start: 73350285
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350286
feature_type: variation
id: rs369870973
seq_region_name: 17
source: dbSNP
start: 73350286
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350289
feature_type: variation
id: rs1274285661
seq_region_name: 17
source: dbSNP
start: 73350289
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350290
feature_type: variation
id: rs1486223231
seq_region_name: 17
source: dbSNP
start: 73350290
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350292
feature_type: variation
id: rs1291854747
seq_region_name: 17
source: dbSNP
start: 73350292
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350296
feature_type: variation
id: rs752640012
seq_region_name: 17
source: dbSNP
start: 73350296
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350300
feature_type: variation
id: rs1568361044
seq_region_name: 17
source: dbSNP
start: 73350300
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73350302
feature_type: variation
id: rs1568361048
seq_region_name: 17
source: dbSNP
start: 73350301
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350304
feature_type: variation
id: rs1235926295
seq_region_name: 17
source: dbSNP
start: 73350304
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350306
feature_type: variation
id: rs756085035
seq_region_name: 17
source: dbSNP
start: 73350306
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350313
feature_type: variation
id: rs1315409840
seq_region_name: 17
source: dbSNP
start: 73350313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350314
feature_type: variation
id: rs2145394644
seq_region_name: 17
source: dbSNP
start: 73350314
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350316
feature_type: variation
id: rs777905116
seq_region_name: 17
source: dbSNP
start: 73350316
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350317
feature_type: variation
id: rs116738350
seq_region_name: 17
source: dbSNP
start: 73350317
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350318
feature_type: variation
id: rs1447517516
seq_region_name: 17
source: dbSNP
start: 73350318
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350325
feature_type: variation
id: rs780265782
seq_region_name: 17
source: dbSNP
start: 73350325
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350329
feature_type: variation
id: rs747218544
seq_region_name: 17
source: dbSNP
start: 73350329
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350335
feature_type: variation
id: rs769026772
seq_region_name: 17
source: dbSNP
start: 73350335
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350337
feature_type: variation
id: rs372386732
seq_region_name: 17
source: dbSNP
start: 73350337
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350338
feature_type: variation
id: rs1413843027
seq_region_name: 17
source: dbSNP
start: 73350338
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350340
feature_type: variation
id: rs139480135
seq_region_name: 17
source: dbSNP
start: 73350340
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350341
feature_type: variation
id: rs773777944
seq_region_name: 17
source: dbSNP
start: 73350341
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350343
feature_type: variation
id: rs2062525884
seq_region_name: 17
source: dbSNP
start: 73350343
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350344
feature_type: variation
id: rs569602552
seq_region_name: 17
source: dbSNP
start: 73350344
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350345
feature_type: variation
id: rs751171693
seq_region_name: 17
source: dbSNP
start: 73350345
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350348
feature_type: variation
id: rs759140095
seq_region_name: 17
source: dbSNP
start: 73350348
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350349
feature_type: variation
id: rs2062526036
seq_region_name: 17
source: dbSNP
start: 73350349
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350351
feature_type: variation
id: rs1212220902
seq_region_name: 17
source: dbSNP
start: 73350351
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350354
feature_type: variation
id: rs1445292098
seq_region_name: 17
source: dbSNP
start: 73350354
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350358
feature_type: variation
id: rs532789356
seq_region_name: 17
source: dbSNP
start: 73350358
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350363
feature_type: variation
id: rs767237872
seq_region_name: 17
source: dbSNP
start: 73350363
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350367
feature_type: variation
id: rs867413079
seq_region_name: 17
source: dbSNP
start: 73350367
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350370
feature_type: variation
id: rs752517423
seq_region_name: 17
source: dbSNP
start: 73350370
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: splice_region_variant
end: 73350374
feature_type: variation
id: rs35317925
seq_region_name: 17
source: dbSNP
start: 73350374
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350381
feature_type: variation
id: rs1306290674
seq_region_name: 17
source: dbSNP
start: 73350381
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350383
feature_type: variation
id: rs753840920
seq_region_name: 17
source: dbSNP
start: 73350383
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350384
feature_type: variation
id: rs376004218
seq_region_name: 17
source: dbSNP
start: 73350384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350386
feature_type: variation
id: rs149660021
seq_region_name: 17
source: dbSNP
start: 73350386
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350387
feature_type: variation
id: rs747154765
seq_region_name: 17
source: dbSNP
start: 73350387
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350388
feature_type: variation
id: rs1463623900
seq_region_name: 17
source: dbSNP
start: 73350388
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350392
feature_type: variation
id: rs1599472589
seq_region_name: 17
source: dbSNP
start: 73350392
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350393
feature_type: variation
id: rs1324134458
seq_region_name: 17
source: dbSNP
start: 73350393
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350394
feature_type: variation
id: rs781453694
seq_region_name: 17
source: dbSNP
start: 73350394
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350400
feature_type: variation
id: rs1395586597
seq_region_name: 17
source: dbSNP
start: 73350400
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350401
feature_type: variation
id: rs748511818
seq_region_name: 17
source: dbSNP
start: 73350401
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350402
feature_type: variation
id: rs2062526631
seq_region_name: 17
source: dbSNP
start: 73350402
strand: 1
-
alleles:
- TTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350404
feature_type: variation
id: rs1400836256
seq_region_name: 17
source: dbSNP
start: 73350402
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350411
feature_type: variation
id: rs1478990168
seq_region_name: 17
source: dbSNP
start: 73350411
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350414
feature_type: variation
id: rs1170581711
seq_region_name: 17
source: dbSNP
start: 73350414
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350416
feature_type: variation
id: rs770153144
seq_region_name: 17
source: dbSNP
start: 73350416
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350417
feature_type: variation
id: rs1289124833
seq_region_name: 17
source: dbSNP
start: 73350417
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350423
feature_type: variation
id: rs979813613
seq_region_name: 17
source: dbSNP
start: 73350423
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350424
feature_type: variation
id: rs1257051873
seq_region_name: 17
source: dbSNP
start: 73350424
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350430
feature_type: variation
id: rs147802955
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs2062526898
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062527014
seq_region_name: 17
source: dbSNP
start: 73350445
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73350446
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs959680519
seq_region_name: 17
source: dbSNP
start: 73350450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527123
seq_region_name: 17
source: dbSNP
start: 73350451
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527152
seq_region_name: 17
source: dbSNP
start: 73350455
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1268896423
seq_region_name: 17
source: dbSNP
start: 73350456
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527209
seq_region_name: 17
source: dbSNP
start: 73350462
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527228
seq_region_name: 17
source: dbSNP
start: 73350470
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527261
seq_region_name: 17
source: dbSNP
start: 73350477
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527285
seq_region_name: 17
source: dbSNP
start: 73350484
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs988463989
seq_region_name: 17
source: dbSNP
start: 73350487
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527352
seq_region_name: 17
source: dbSNP
start: 73350490
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs913110150
seq_region_name: 17
source: dbSNP
start: 73350492
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs186667264
seq_region_name: 17
source: dbSNP
start: 73350494
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1428215183
seq_region_name: 17
source: dbSNP
start: 73350500
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs141196259
seq_region_name: 17
source: dbSNP
start: 73350503
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350504
feature_type: variation
id: rs1599472693
seq_region_name: 17
source: dbSNP
start: 73350504
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062527546
seq_region_name: 17
source: dbSNP
start: 73350505
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350508
feature_type: variation
id: rs2062527567
seq_region_name: 17
source: dbSNP
start: 73350508
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599472700
seq_region_name: 17
source: dbSNP
start: 73350514
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs978960368
seq_region_name: 17
source: dbSNP
start: 73350517
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350518
feature_type: variation
id: rs921798525
seq_region_name: 17
source: dbSNP
start: 73350518
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1251369749
seq_region_name: 17
source: dbSNP
start: 73350520
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350521
feature_type: variation
id: rs2062527679
seq_region_name: 17
source: dbSNP
start: 73350521
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350532
feature_type: variation
id: rs2062527708
seq_region_name: 17
source: dbSNP
start: 73350532
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350534
feature_type: variation
id: rs1213318854
seq_region_name: 17
source: dbSNP
start: 73350534
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350535
feature_type: variation
id: rs1335826307
seq_region_name: 17
source: dbSNP
start: 73350535
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350543
feature_type: variation
id: rs1599472728
seq_region_name: 17
source: dbSNP
start: 73350543
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs189944854
seq_region_name: 17
source: dbSNP
start: 73350546
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350547
feature_type: variation
id: rs953425430
seq_region_name: 17
source: dbSNP
start: 73350547
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350548
feature_type: variation
id: rs2062527855
seq_region_name: 17
source: dbSNP
start: 73350548
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350550
feature_type: variation
id: rs2062527882
seq_region_name: 17
source: dbSNP
start: 73350550
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350552
feature_type: variation
id: rs570393817
seq_region_name: 17
source: dbSNP
start: 73350552
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350554
feature_type: variation
id: rs1599472746
seq_region_name: 17
source: dbSNP
start: 73350554
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350555
feature_type: variation
id: rs2062527953
seq_region_name: 17
source: dbSNP
start: 73350555
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350556
feature_type: variation
id: rs2062527976
seq_region_name: 17
source: dbSNP
start: 73350556
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350560
feature_type: variation
id: rs1599472750
seq_region_name: 17
source: dbSNP
start: 73350560
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350562
feature_type: variation
id: rs1271328147
seq_region_name: 17
source: dbSNP
start: 73350562
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350566
feature_type: variation
id: rs2062528053
seq_region_name: 17
source: dbSNP
start: 73350566
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350567
feature_type: variation
id: rs1430823686
seq_region_name: 17
source: dbSNP
start: 73350567
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350568
feature_type: variation
id: rs1366815423
seq_region_name: 17
source: dbSNP
start: 73350568
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350571
feature_type: variation
id: rs1323403659
seq_region_name: 17
source: dbSNP
start: 73350570
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350572
feature_type: variation
id: rs1439709118
seq_region_name: 17
source: dbSNP
start: 73350572
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350578
feature_type: variation
id: rs912006473
seq_region_name: 17
source: dbSNP
start: 73350578
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350579
feature_type: variation
id: rs534579286
seq_region_name: 17
source: dbSNP
start: 73350579
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350582
feature_type: variation
id: rs538168947
seq_region_name: 17
source: dbSNP
start: 73350582
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350583
feature_type: variation
id: rs1308038981
seq_region_name: 17
source: dbSNP
start: 73350583
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350585
feature_type: variation
id: rs1366264974
seq_region_name: 17
source: dbSNP
start: 73350585
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350598
feature_type: variation
id: rs2062528314
seq_region_name: 17
source: dbSNP
start: 73350598
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350599
feature_type: variation
id: rs2062528333
seq_region_name: 17
source: dbSNP
start: 73350599
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350602
feature_type: variation
id: rs202068153
seq_region_name: 17
source: dbSNP
start: 73350602
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350604
feature_type: variation
id: rs749778543
seq_region_name: 17
source: dbSNP
start: 73350604
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350605
feature_type: variation
id: rs1385749560
seq_region_name: 17
source: dbSNP
start: 73350605
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350606
feature_type: variation
id: rs369215097
seq_region_name: 17
source: dbSNP
start: 73350606
strand: 1
-
alleles:
- AAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350610
feature_type: variation
id: rs2062528498
seq_region_name: 17
source: dbSNP
start: 73350607
strand: 1
-
alleles:
- AACTCAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350615
feature_type: variation
id: rs2062528523
seq_region_name: 17
source: dbSNP
start: 73350609
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350610
feature_type: variation
id: rs2062528547
seq_region_name: 17
source: dbSNP
start: 73350610
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350611
feature_type: variation
id: rs1995163
seq_region_name: 17
source: dbSNP
start: 73350611
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350613
feature_type: variation
id: rs1036379176
seq_region_name: 17
source: dbSNP
start: 73350613
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350614
feature_type: variation
id: rs556777830
seq_region_name: 17
source: dbSNP
start: 73350614
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350616
feature_type: variation
id: rs2062528684
seq_region_name: 17
source: dbSNP
start: 73350616
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350620
feature_type: variation
id: rs995102833
seq_region_name: 17
source: dbSNP
start: 73350620
strand: 1
-
alleles:
- GCCAGCATGGC
- GC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350631
feature_type: variation
id: rs1439289479
seq_region_name: 17
source: dbSNP
start: 73350621
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350623
feature_type: variation
id: rs2062528761
seq_region_name: 17
source: dbSNP
start: 73350623
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350625
feature_type: variation
id: rs1253407688
seq_region_name: 17
source: dbSNP
start: 73350625
strand: 1
-
alleles:
- GCATGGCTG
- GCATGGCTGCATGGCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350633
feature_type: variation
id: rs2062528813
seq_region_name: 17
source: dbSNP
start: 73350625
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350626
feature_type: variation
id: rs1045761406
seq_region_name: 17
source: dbSNP
start: 73350626
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350627
feature_type: variation
id: rs905366621
seq_region_name: 17
source: dbSNP
start: 73350627
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350628
feature_type: variation
id: rs2145395501
seq_region_name: 17
source: dbSNP
start: 73350628
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350630
feature_type: variation
id: rs1273378580
seq_region_name: 17
source: dbSNP
start: 73350630
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350633
feature_type: variation
id: rs1344752716
seq_region_name: 17
source: dbSNP
start: 73350633
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350634
feature_type: variation
id: rs1224502848
seq_region_name: 17
source: dbSNP
start: 73350634
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350635
feature_type: variation
id: rs767062535
seq_region_name: 17
source: dbSNP
start: 73350635
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350638
feature_type: variation
id: rs377641221
seq_region_name: 17
source: dbSNP
start: 73350638
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350640
feature_type: variation
id: rs1208150453
seq_region_name: 17
source: dbSNP
start: 73350640
strand: 1
-
alleles:
- CTCACTCAC
- CTCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73350649
feature_type: variation
id: rs2062529080
seq_region_name: 17
source: dbSNP
start: 73350641
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350643
feature_type: variation
id: rs760479146
seq_region_name: 17
source: dbSNP
start: 73350643
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350650
feature_type: variation
id: rs2062529148
seq_region_name: 17
source: dbSNP
start: 73350650
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350651
feature_type: variation
id: rs371077392
seq_region_name: 17
source: dbSNP
start: 73350651
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350652
feature_type: variation
id: rs753787922
seq_region_name: 17
source: dbSNP
start: 73350652
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350655
feature_type: variation
id: rs757113301
seq_region_name: 17
source: dbSNP
start: 73350655
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350660
feature_type: variation
id: rs2062529238
seq_region_name: 17
source: dbSNP
start: 73350660
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350665
feature_type: variation
id: rs1470404702
seq_region_name: 17
source: dbSNP
start: 73350665
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350667
feature_type: variation
id: rs1161167826
seq_region_name: 17
source: dbSNP
start: 73350667
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350668
feature_type: variation
id: rs575236854
seq_region_name: 17
source: dbSNP
start: 73350668
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350669
feature_type: variation
id: rs539426717
seq_region_name: 17
source: dbSNP
start: 73350669
strand: 1
-
alleles:
- CTTCTTGCTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73350682
feature_type: variation
id: rs750289460
seq_region_name: 17
source: dbSNP
start: 73350672
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350675
feature_type: variation
id: rs1274312402
seq_region_name: 17
source: dbSNP
start: 73350675
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350678
feature_type: variation
id: rs930517187
seq_region_name: 17
source: dbSNP
start: 73350678
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350682
feature_type: variation
id: rs755155850
seq_region_name: 17
source: dbSNP
start: 73350682
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350687
feature_type: variation
id: rs1343588531
seq_region_name: 17
source: dbSNP
start: 73350687
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350688
feature_type: variation
id: rs373850295
seq_region_name: 17
source: dbSNP
start: 73350688
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350689
feature_type: variation
id: rs748387140
seq_region_name: 17
source: dbSNP
start: 73350689
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350690
feature_type: variation
id: rs142861586
seq_region_name: 17
source: dbSNP
start: 73350690
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350693
feature_type: variation
id: rs1290639795
seq_region_name: 17
source: dbSNP
start: 73350693
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350695
feature_type: variation
id: rs1294965094
seq_region_name: 17
source: dbSNP
start: 73350695
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350696
feature_type: variation
id: rs2062529750
seq_region_name: 17
source: dbSNP
start: 73350696
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350699
feature_type: variation
id: rs778137775
seq_region_name: 17
source: dbSNP
start: 73350699
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350700
feature_type: variation
id: rs2062529817
seq_region_name: 17
source: dbSNP
start: 73350700
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350701
feature_type: variation
id: rs980554263
seq_region_name: 17
source: dbSNP
start: 73350701
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350702
feature_type: variation
id: rs749699574
seq_region_name: 17
source: dbSNP
start: 73350702
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350705
feature_type: variation
id: rs1431586223
seq_region_name: 17
source: dbSNP
start: 73350705
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350714
feature_type: variation
id: rs771318640
seq_region_name: 17
source: dbSNP
start: 73350714
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350719
feature_type: variation
id: rs1207938130
seq_region_name: 17
source: dbSNP
start: 73350719
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350722
feature_type: variation
id: rs2062530030
seq_region_name: 17
source: dbSNP
start: 73350722
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350724
feature_type: variation
id: rs775772636
seq_region_name: 17
source: dbSNP
start: 73350724
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350725
feature_type: variation
id: rs1599473000
seq_region_name: 17
source: dbSNP
start: 73350725
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350726
feature_type: variation
id: rs2062530135
seq_region_name: 17
source: dbSNP
start: 73350726
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350728
feature_type: variation
id: rs1173065634
seq_region_name: 17
source: dbSNP
start: 73350728
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350731
feature_type: variation
id: rs1019949009
seq_region_name: 17
source: dbSNP
start: 73350731
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350732
feature_type: variation
id: rs79391654
seq_region_name: 17
source: dbSNP
start: 73350732
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350734
feature_type: variation
id: rs969004153
seq_region_name: 17
source: dbSNP
start: 73350734
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350735
feature_type: variation
id: rs1249416949
seq_region_name: 17
source: dbSNP
start: 73350735
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350737
feature_type: variation
id: rs978695707
seq_region_name: 17
source: dbSNP
start: 73350737
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350738
feature_type: variation
id: rs1233819195
seq_region_name: 17
source: dbSNP
start: 73350738
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350739
feature_type: variation
id: rs774979076
seq_region_name: 17
source: dbSNP
start: 73350739
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350740
feature_type: variation
id: rs921886029
seq_region_name: 17
source: dbSNP
start: 73350740
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350744
feature_type: variation
id: rs1369647985
seq_region_name: 17
source: dbSNP
start: 73350744
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350747
feature_type: variation
id: rs2062530458
seq_region_name: 17
source: dbSNP
start: 73350747
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350749
feature_type: variation
id: rs2062530496
seq_region_name: 17
source: dbSNP
start: 73350749
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350750
feature_type: variation
id: rs183083087
seq_region_name: 17
source: dbSNP
start: 73350750
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350751
feature_type: variation
id: rs745365412
seq_region_name: 17
source: dbSNP
start: 73350751
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350753
feature_type: variation
id: rs953174501
seq_region_name: 17
source: dbSNP
start: 73350753
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73350762
feature_type: variation
id: rs1280296336
seq_region_name: 17
source: dbSNP
start: 73350762
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350767
feature_type: variation
id: rs2062530681
seq_region_name: 17
source: dbSNP
start: 73350767
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73350777
feature_type: variation
id: rs1209486264
seq_region_name: 17
source: dbSNP
start: 73350774
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350778
feature_type: variation
id: rs769454639
seq_region_name: 17
source: dbSNP
start: 73350778
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73350782
feature_type: variation
id: rs370520611
seq_region_name: 17
source: dbSNP
start: 73350782
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73350783
feature_type: variation
id: rs147438025
seq_region_name: 17
source: dbSNP
start: 73350783
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350793
feature_type: variation
id: rs2062530831
seq_region_name: 17
source: dbSNP
start: 73350793
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350796
feature_type: variation
id: rs2145396048
seq_region_name: 17
source: dbSNP
start: 73350796
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350797
feature_type: variation
id: rs1369103245
seq_region_name: 17
source: dbSNP
start: 73350797
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73350798
feature_type: variation
id: rs1372564935
seq_region_name: 17
source: dbSNP
start: 73350798
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350800
feature_type: variation
id: rs2062530915
seq_region_name: 17
source: dbSNP
start: 73350800
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350804
feature_type: variation
id: rs4969107
seq_region_name: 17
source: dbSNP
start: 73350804
strand: 1
-
alleles:
- AGTCAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350809
feature_type: variation
id: rs1221729794
seq_region_name: 17
source: dbSNP
start: 73350804
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73350805
feature_type: variation
id: rs1302720646
seq_region_name: 17
source: dbSNP
start: 73350805
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350808
feature_type: variation
id: rs201242790
seq_region_name: 17
source: dbSNP
start: 73350808
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350809
feature_type: variation
id: rs761727474
seq_region_name: 17
source: dbSNP
start: 73350809
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350810
feature_type: variation
id: rs765084920
seq_region_name: 17
source: dbSNP
start: 73350810
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350811
feature_type: variation
id: rs1411486131
seq_region_name: 17
source: dbSNP
start: 73350811
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350815
feature_type: variation
id: rs750381784
seq_region_name: 17
source: dbSNP
start: 73350815
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350818
feature_type: variation
id: rs1342773532
seq_region_name: 17
source: dbSNP
start: 73350818
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350819
feature_type: variation
id: rs1568361333
seq_region_name: 17
source: dbSNP
start: 73350819
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350823
feature_type: variation
id: rs2062531292
seq_region_name: 17
source: dbSNP
start: 73350823
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350827
feature_type: variation
id: rs754958761
seq_region_name: 17
source: dbSNP
start: 73350827
strand: 1
-
alleles:
- CCCCC
- CC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350831
feature_type: variation
id: rs762626556
seq_region_name: 17
source: dbSNP
start: 73350827
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350828
feature_type: variation
id: rs1482621156
seq_region_name: 17
source: dbSNP
start: 73350828
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350829
feature_type: variation
id: rs920615125
seq_region_name: 17
source: dbSNP
start: 73350829
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350832
feature_type: variation
id: rs1312273733
seq_region_name: 17
source: dbSNP
start: 73350832
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350833
feature_type: variation
id: rs2062531453
seq_region_name: 17
source: dbSNP
start: 73350833
strand: 1
-
alleles:
- CCTCCCTCC
- CCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350841
feature_type: variation
id: rs1466608636
seq_region_name: 17
source: dbSNP
start: 73350833
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350834
feature_type: variation
id: rs2145396169
seq_region_name: 17
source: dbSNP
start: 73350834
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350836
feature_type: variation
id: rs2062531512
seq_region_name: 17
source: dbSNP
start: 73350836
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350838
feature_type: variation
id: rs766088843
seq_region_name: 17
source: dbSNP
start: 73350836
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350839
feature_type: variation
id: rs1365784356
seq_region_name: 17
source: dbSNP
start: 73350839
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350846
feature_type: variation
id: rs187936625
seq_region_name: 17
source: dbSNP
start: 73350846
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350848
feature_type: variation
id: rs2062531626
seq_region_name: 17
source: dbSNP
start: 73350848
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350851
feature_type: variation
id: rs2062531650
seq_region_name: 17
source: dbSNP
start: 73350851
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350855
feature_type: variation
id: rs1386448830
seq_region_name: 17
source: dbSNP
start: 73350855
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350860
feature_type: variation
id: rs1418749562
seq_region_name: 17
source: dbSNP
start: 73350860
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350866
feature_type: variation
id: rs2062531742
seq_region_name: 17
source: dbSNP
start: 73350866
strand: 1
-
alleles:
- CTAACTGCTA
- CTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350878
feature_type: variation
id: rs1409107332
seq_region_name: 17
source: dbSNP
start: 73350869
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73350874
feature_type: variation
id: rs1184752316
seq_region_name: 17
source: dbSNP
start: 73350874
strand: 1
-
alleles:
- C
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351000
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73351009
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351013
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351020
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351023
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351024
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351026
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351029
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351033
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351037
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73351040
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73351045
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351052
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351053
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351054
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351057
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351064
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351066
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351068
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351069
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351071
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351073
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73351074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351075
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351076
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351078
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351080
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351081
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1438990099
seq_region_name: 17
source: dbSNP
start: 73351083
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351085
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351086
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs889291612
seq_region_name: 17
source: dbSNP
start: 73351089
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73351091
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351091
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351092
feature_type: variation
id: rs2145396776
seq_region_name: 17
source: dbSNP
start: 73351092
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351094
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351097
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351097
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351104
feature_type: variation
id: rs2062534006
seq_region_name: 17
source: dbSNP
start: 73351104
strand: 1
-
alleles:
- TTTTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351108
feature_type: variation
id: rs140083285
seq_region_name: 17
source: dbSNP
start: 73351104
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- TTTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062534439
seq_region_name: 17
source: dbSNP
start: 73351114
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs796314694
seq_region_name: 17
source: dbSNP
start: 73351114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351116
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351118
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351119
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351120
strand: 1
-
alleles:
- TT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351120
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351126
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1384736824
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1394795951
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062534767
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351129
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351134
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351141
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351145
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351162
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73351164
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351167
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351181
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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id: rs930647170
seq_region_name: 17
source: dbSNP
start: 73351185
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568361511
seq_region_name: 17
source: dbSNP
start: 73351186
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs557795879
seq_region_name: 17
source: dbSNP
start: 73351190
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1195115660
seq_region_name: 17
source: dbSNP
start: 73351191
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062535303
seq_region_name: 17
source: dbSNP
start: 73351192
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062535338
seq_region_name: 17
source: dbSNP
start: 73351195
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs572829904
seq_region_name: 17
source: dbSNP
start: 73351198
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs981192699
seq_region_name: 17
source: dbSNP
start: 73351200
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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end: 73351201
feature_type: variation
id: rs2062535415
seq_region_name: 17
source: dbSNP
start: 73351201
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351202
feature_type: variation
id: rs1276736866
seq_region_name: 17
source: dbSNP
start: 73351202
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs535383596
seq_region_name: 17
source: dbSNP
start: 73351203
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351206
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062535527
seq_region_name: 17
source: dbSNP
start: 73351207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1347316810
seq_region_name: 17
source: dbSNP
start: 73351208
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062535587
seq_region_name: 17
source: dbSNP
start: 73351209
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351214
feature_type: variation
id: rs1275600110
seq_region_name: 17
source: dbSNP
start: 73351214
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351218
feature_type: variation
id: rs1599473584
seq_region_name: 17
source: dbSNP
start: 73351218
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351219
feature_type: variation
id: rs1256128888
seq_region_name: 17
source: dbSNP
start: 73351219
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351225
feature_type: variation
id: rs2062535687
seq_region_name: 17
source: dbSNP
start: 73351225
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351228
feature_type: variation
id: rs2062535711
seq_region_name: 17
source: dbSNP
start: 73351228
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351236
feature_type: variation
id: rs2062535739
seq_region_name: 17
source: dbSNP
start: 73351236
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351242
feature_type: variation
id: rs2062535765
seq_region_name: 17
source: dbSNP
start: 73351242
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351244
feature_type: variation
id: rs1334305305
seq_region_name: 17
source: dbSNP
start: 73351244
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351245
feature_type: variation
id: rs1306760260
seq_region_name: 17
source: dbSNP
start: 73351245
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351248
feature_type: variation
id: rs1410885171
seq_region_name: 17
source: dbSNP
start: 73351248
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351253
feature_type: variation
id: rs1420238744
seq_region_name: 17
source: dbSNP
start: 73351253
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351254
feature_type: variation
id: rs2145397209
seq_region_name: 17
source: dbSNP
start: 73351254
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351255
feature_type: variation
id: rs1599473602
seq_region_name: 17
source: dbSNP
start: 73351255
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351256
feature_type: variation
id: rs2062535916
seq_region_name: 17
source: dbSNP
start: 73351256
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351261
feature_type: variation
id: rs2062535941
seq_region_name: 17
source: dbSNP
start: 73351256
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351257
feature_type: variation
id: rs1311667119
seq_region_name: 17
source: dbSNP
start: 73351257
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351266
feature_type: variation
id: rs926851853
seq_region_name: 17
source: dbSNP
start: 73351266
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351268
feature_type: variation
id: rs2062535988
seq_region_name: 17
source: dbSNP
start: 73351268
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351270
feature_type: variation
id: rs541810387
seq_region_name: 17
source: dbSNP
start: 73351270
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351271
feature_type: variation
id: rs755137965
seq_region_name: 17
source: dbSNP
start: 73351271
strand: 1
-
alleles:
- AA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351276
feature_type: variation
id: rs2062536085
seq_region_name: 17
source: dbSNP
start: 73351275
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351280
feature_type: variation
id: rs2062536120
seq_region_name: 17
source: dbSNP
start: 73351280
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351282
feature_type: variation
id: rs2062536145
seq_region_name: 17
source: dbSNP
start: 73351282
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351284
feature_type: variation
id: rs2062536165
seq_region_name: 17
source: dbSNP
start: 73351284
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351289
feature_type: variation
id: rs373134979
seq_region_name: 17
source: dbSNP
start: 73351289
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351296
feature_type: variation
id: rs1599473647
seq_region_name: 17
source: dbSNP
start: 73351296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351298
feature_type: variation
id: rs1177509416
seq_region_name: 17
source: dbSNP
start: 73351298
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351299
feature_type: variation
id: rs1888574997
seq_region_name: 17
source: dbSNP
start: 73351299
strand: 1
-
alleles:
- GGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351302
feature_type: variation
id: rs2062536274
seq_region_name: 17
source: dbSNP
start: 73351299
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351303
feature_type: variation
id: rs966475171
seq_region_name: 17
source: dbSNP
start: 73351303
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351306
feature_type: variation
id: rs945577655
seq_region_name: 17
source: dbSNP
start: 73351306
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73351421
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73351448
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73351453
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351456
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73351462
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73351464
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73351469
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351471
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73351472
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs923350176
seq_region_name: 17
source: dbSNP
start: 73351477
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73351483
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351484
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351489
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351493
strand: 1
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alleles:
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- "-"
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73351498
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351501
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351502
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351505
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351507
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351512
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351514
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351519
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351520
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351521
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs1296447360
seq_region_name: 17
source: dbSNP
start: 73351530
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1366873937
seq_region_name: 17
source: dbSNP
start: 73351534
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351537
feature_type: variation
id: rs115672714
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs929428608
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1049167397
seq_region_name: 17
source: dbSNP
start: 73351579
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062538877
seq_region_name: 17
source: dbSNP
start: 73351582
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1478521829
seq_region_name: 17
source: dbSNP
start: 73351592
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062538934
seq_region_name: 17
source: dbSNP
start: 73351598
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs775083627
seq_region_name: 17
source: dbSNP
start: 73351599
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1248850000
seq_region_name: 17
source: dbSNP
start: 73351606
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1202974215
seq_region_name: 17
source: dbSNP
start: 73351607
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062539050
seq_region_name: 17
source: dbSNP
start: 73351608
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351612
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs768637639
seq_region_name: 17
source: dbSNP
start: 73351614
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351615
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351621
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351621
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351622
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351630
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351634
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351637
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062539390
seq_region_name: 17
source: dbSNP
start: 73351638
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351640
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351642
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351646
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351650
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351654
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351655
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351662
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351667
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062539664
seq_region_name: 17
source: dbSNP
start: 73351672
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351673
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351678
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73351679
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs761607540
seq_region_name: 17
source: dbSNP
start: 73351681
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1373715095
seq_region_name: 17
source: dbSNP
start: 73351682
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351697
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351698
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351707
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs992150980
seq_region_name: 17
source: dbSNP
start: 73351708
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062540029
seq_region_name: 17
source: dbSNP
start: 73351711
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145398361
seq_region_name: 17
source: dbSNP
start: 73351712
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs914131274
seq_region_name: 17
source: dbSNP
start: 73351721
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs967384887
seq_region_name: 17
source: dbSNP
start: 73351727
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs566512197
seq_region_name: 17
source: dbSNP
start: 73351731
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062540179
seq_region_name: 17
source: dbSNP
start: 73351735
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs374089194
seq_region_name: 17
source: dbSNP
start: 73351736
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062540263
seq_region_name: 17
source: dbSNP
start: 73351739
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062540306
seq_region_name: 17
source: dbSNP
start: 73351741
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351742
feature_type: variation
id: rs2062540342
seq_region_name: 17
source: dbSNP
start: 73351742
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1472505186
seq_region_name: 17
source: dbSNP
start: 73351745
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs976367948
seq_region_name: 17
source: dbSNP
start: 73351746
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062540487
seq_region_name: 17
source: dbSNP
start: 73351751
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1184993974
seq_region_name: 17
source: dbSNP
start: 73351751
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351752
feature_type: variation
id: rs2062540577
seq_region_name: 17
source: dbSNP
start: 73351752
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062540619
seq_region_name: 17
source: dbSNP
start: 73351756
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351759
feature_type: variation
id: rs1483713413
seq_region_name: 17
source: dbSNP
start: 73351759
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1253774071
seq_region_name: 17
source: dbSNP
start: 73351760
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351763
feature_type: variation
id: rs919492352
seq_region_name: 17
source: dbSNP
start: 73351763
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1312389620
seq_region_name: 17
source: dbSNP
start: 73351765
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351766
feature_type: variation
id: rs2062540786
seq_region_name: 17
source: dbSNP
start: 73351766
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599474090
seq_region_name: 17
source: dbSNP
start: 73351767
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351769
feature_type: variation
id: rs1280347512
seq_region_name: 17
source: dbSNP
start: 73351769
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351770
feature_type: variation
id: rs533535682
seq_region_name: 17
source: dbSNP
start: 73351770
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351771
feature_type: variation
id: rs1328238848
seq_region_name: 17
source: dbSNP
start: 73351771
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351775
feature_type: variation
id: rs2062540912
seq_region_name: 17
source: dbSNP
start: 73351775
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351778
feature_type: variation
id: rs1288833056
seq_region_name: 17
source: dbSNP
start: 73351778
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351781
feature_type: variation
id: rs1487592917
seq_region_name: 17
source: dbSNP
start: 73351781
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351782
feature_type: variation
id: rs1190830892
seq_region_name: 17
source: dbSNP
start: 73351782
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351785
feature_type: variation
id: rs2062541007
seq_region_name: 17
source: dbSNP
start: 73351785
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351786
feature_type: variation
id: rs2062541040
seq_region_name: 17
source: dbSNP
start: 73351786
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351787
feature_type: variation
id: rs1411616544
seq_region_name: 17
source: dbSNP
start: 73351787
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351788
feature_type: variation
id: rs984904008
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source: dbSNP
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-
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351868
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351879
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351881
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351886
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351889
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351891
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73351897
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73351899
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351900
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73351900
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351901
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351902
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351903
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351905
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73351908
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73351910
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062542210
seq_region_name: 17
source: dbSNP
start: 73351911
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351918
feature_type: variation
id: rs887602945
seq_region_name: 17
source: dbSNP
start: 73351918
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351921
feature_type: variation
id: rs1166183795
seq_region_name: 17
source: dbSNP
start: 73351921
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351922
feature_type: variation
id: rs7342840
seq_region_name: 17
source: dbSNP
start: 73351922
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351927
feature_type: variation
id: rs1033713953
seq_region_name: 17
source: dbSNP
start: 73351927
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351928
feature_type: variation
id: rs2062542354
seq_region_name: 17
source: dbSNP
start: 73351927
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351932
feature_type: variation
id: rs1342007652
seq_region_name: 17
source: dbSNP
start: 73351932
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351933
feature_type: variation
id: rs1568361762
seq_region_name: 17
source: dbSNP
start: 73351933
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351935
feature_type: variation
id: rs2062542422
seq_region_name: 17
source: dbSNP
start: 73351935
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1247360122
seq_region_name: 17
source: dbSNP
start: 73351936
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351939
feature_type: variation
id: rs1464143997
seq_region_name: 17
source: dbSNP
start: 73351939
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351943
feature_type: variation
id: rs1248299786
seq_region_name: 17
source: dbSNP
start: 73351943
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351947
feature_type: variation
id: rs572936700
seq_region_name: 17
source: dbSNP
start: 73351947
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351951
feature_type: variation
id: rs2062542547
seq_region_name: 17
source: dbSNP
start: 73351951
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351952
feature_type: variation
id: rs1450006596
seq_region_name: 17
source: dbSNP
start: 73351952
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351955
feature_type: variation
id: rs1264728805
seq_region_name: 17
source: dbSNP
start: 73351955
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351957
feature_type: variation
id: rs748240875
seq_region_name: 17
source: dbSNP
start: 73351955
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351959
feature_type: variation
id: rs1242962684
seq_region_name: 17
source: dbSNP
start: 73351959
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351961
feature_type: variation
id: rs2145399021
seq_region_name: 17
source: dbSNP
start: 73351961
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351968
feature_type: variation
id: rs2062542668
seq_region_name: 17
source: dbSNP
start: 73351968
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351969
feature_type: variation
id: rs2062542696
seq_region_name: 17
source: dbSNP
start: 73351969
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351970
feature_type: variation
id: rs1323542517
seq_region_name: 17
source: dbSNP
start: 73351970
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351977
feature_type: variation
id: rs2145399048
seq_region_name: 17
source: dbSNP
start: 73351978
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351978
feature_type: variation
id: rs761018384
seq_region_name: 17
source: dbSNP
start: 73351978
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351979
feature_type: variation
id: rs1013518876
seq_region_name: 17
source: dbSNP
start: 73351979
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351980
feature_type: variation
id: rs1247197638
seq_region_name: 17
source: dbSNP
start: 73351980
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351983
feature_type: variation
id: rs2062542824
seq_region_name: 17
source: dbSNP
start: 73351983
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351986
feature_type: variation
id: rs2062542851
seq_region_name: 17
source: dbSNP
start: 73351986
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351989
feature_type: variation
id: rs2062542876
seq_region_name: 17
source: dbSNP
start: 73351989
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351994
feature_type: variation
id: rs2062542909
seq_region_name: 17
source: dbSNP
start: 73351994
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73351995
feature_type: variation
id: rs2062542932
seq_region_name: 17
source: dbSNP
start: 73351995
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352002
feature_type: variation
id: rs965104775
seq_region_name: 17
source: dbSNP
start: 73352002
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352006
feature_type: variation
id: rs1568361790
seq_region_name: 17
source: dbSNP
start: 73352006
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352008
feature_type: variation
id: rs2062542983
seq_region_name: 17
source: dbSNP
start: 73352008
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352011
feature_type: variation
id: rs2062543004
seq_region_name: 17
source: dbSNP
start: 73352011
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352014
feature_type: variation
id: rs2062543029
seq_region_name: 17
source: dbSNP
start: 73352014
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352020
feature_type: variation
id: rs192353004
seq_region_name: 17
source: dbSNP
start: 73352020
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352105
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1330835051
seq_region_name: 17
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start: 73352114
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73352115
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73352117
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352128
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73352134
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1040003301
seq_region_name: 17
source: dbSNP
start: 73352137
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73352137
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352142
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352148
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1169248337
seq_region_name: 17
source: dbSNP
start: 73352149
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352150
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352156
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352157
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352158
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352162
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352163
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1886905467
seq_region_name: 17
source: dbSNP
start: 73352170
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352172
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1481334264
seq_region_name: 17
source: dbSNP
start: 73352173
strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352180
feature_type: variation
id: rs201553880
seq_region_name: 17
source: dbSNP
start: 73352180
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1318906862
seq_region_name: 17
source: dbSNP
start: 73352182
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1254097295
seq_region_name: 17
source: dbSNP
start: 73352184
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062544589
seq_region_name: 17
source: dbSNP
start: 73352187
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1198848696
seq_region_name: 17
source: dbSNP
start: 73352191
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs755334426
seq_region_name: 17
source: dbSNP
start: 73352192
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062544664
seq_region_name: 17
source: dbSNP
start: 73352197
strand: 1
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alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352198
feature_type: variation
id: rs1256879233
seq_region_name: 17
source: dbSNP
start: 73352198
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062544714
seq_region_name: 17
source: dbSNP
start: 73352202
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352203
feature_type: variation
id: rs1235864849
seq_region_name: 17
source: dbSNP
start: 73352203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352206
feature_type: variation
id: rs1296551727
seq_region_name: 17
source: dbSNP
start: 73352206
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352210
feature_type: variation
id: rs551532638
seq_region_name: 17
source: dbSNP
start: 73352210
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352212
feature_type: variation
id: rs2062544803
seq_region_name: 17
source: dbSNP
start: 73352212
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352213
feature_type: variation
id: rs2062544828
seq_region_name: 17
source: dbSNP
start: 73352213
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs889630828
seq_region_name: 17
source: dbSNP
start: 73352218
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352220
feature_type: variation
id: rs2062544873
seq_region_name: 17
source: dbSNP
start: 73352220
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352224
feature_type: variation
id: rs2062544897
seq_region_name: 17
source: dbSNP
start: 73352224
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352228
feature_type: variation
id: rs2062544925
seq_region_name: 17
source: dbSNP
start: 73352228
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352229
feature_type: variation
id: rs2062544942
seq_region_name: 17
source: dbSNP
start: 73352229
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352235
feature_type: variation
id: rs1006718745
seq_region_name: 17
source: dbSNP
start: 73352235
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352236
feature_type: variation
id: rs1350517569
seq_region_name: 17
source: dbSNP
start: 73352236
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352239
feature_type: variation
id: rs1054905144
seq_region_name: 17
source: dbSNP
start: 73352239
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352241
feature_type: variation
id: rs2062545053
seq_region_name: 17
source: dbSNP
start: 73352241
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352244
feature_type: variation
id: rs1040838240
seq_region_name: 17
source: dbSNP
start: 73352244
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352248
feature_type: variation
id: rs896538067
seq_region_name: 17
source: dbSNP
start: 73352248
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352251
feature_type: variation
id: rs73343836
seq_region_name: 17
source: dbSNP
start: 73352251
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352252
feature_type: variation
id: rs1172859921
seq_region_name: 17
source: dbSNP
start: 73352252
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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start: 73352256
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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start: 73352260
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs76751539
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source: dbSNP
start: 73352265
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73352266
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1365506051
seq_region_name: 17
source: dbSNP
start: 73352269
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062545315
seq_region_name: 17
source: dbSNP
start: 73352273
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062545339
seq_region_name: 17
source: dbSNP
start: 73352279
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs571828237
seq_region_name: 17
source: dbSNP
start: 73352280
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352283
feature_type: variation
id: rs1441970995
seq_region_name: 17
source: dbSNP
start: 73352283
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1006433456
seq_region_name: 17
source: dbSNP
start: 73352284
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1205809972
seq_region_name: 17
source: dbSNP
start: 73352297
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352298
feature_type: variation
id: rs1016438397
seq_region_name: 17
source: dbSNP
start: 73352298
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352304
feature_type: variation
id: rs2062545479
seq_region_name: 17
source: dbSNP
start: 73352304
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352305
feature_type: variation
id: rs567215072
seq_region_name: 17
source: dbSNP
start: 73352305
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352309
feature_type: variation
id: rs1267922117
seq_region_name: 17
source: dbSNP
start: 73352309
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352311
feature_type: variation
id: rs1229452893
seq_region_name: 17
source: dbSNP
start: 73352311
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352315
feature_type: variation
id: rs2062545557
seq_region_name: 17
source: dbSNP
start: 73352315
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352317
feature_type: variation
id: rs2062545591
seq_region_name: 17
source: dbSNP
start: 73352317
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352325
feature_type: variation
id: rs2062545615
seq_region_name: 17
source: dbSNP
start: 73352325
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352326
feature_type: variation
id: rs2062545638
seq_region_name: 17
source: dbSNP
start: 73352326
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352330
feature_type: variation
id: rs1331805084
seq_region_name: 17
source: dbSNP
start: 73352330
strand: 1
-
alleles:
- ACAGCCCCGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352340
feature_type: variation
id: rs2062545687
seq_region_name: 17
source: dbSNP
start: 73352331
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352335
feature_type: variation
id: rs2062545705
seq_region_name: 17
source: dbSNP
start: 73352335
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352338
feature_type: variation
id: rs1283016238
seq_region_name: 17
source: dbSNP
start: 73352335
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352336
feature_type: variation
id: rs2062545759
seq_region_name: 17
source: dbSNP
start: 73352336
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs368983415
seq_region_name: 17
source: dbSNP
start: 73352337
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352338
feature_type: variation
id: rs991393910
seq_region_name: 17
source: dbSNP
start: 73352338
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352339
feature_type: variation
id: rs111595834
seq_region_name: 17
source: dbSNP
start: 73352339
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352340
feature_type: variation
id: rs184649364
seq_region_name: 17
source: dbSNP
start: 73352340
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352341
feature_type: variation
id: rs2145399846
seq_region_name: 17
source: dbSNP
start: 73352341
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352344
feature_type: variation
id: rs971208084
seq_region_name: 17
source: dbSNP
start: 73352344
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352346
feature_type: variation
id: rs1454277342
seq_region_name: 17
source: dbSNP
start: 73352346
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1455260093
seq_region_name: 17
source: dbSNP
start: 73352348
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352353
feature_type: variation
id: rs1319606699
seq_region_name: 17
source: dbSNP
start: 73352349
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352351
feature_type: variation
id: rs2145399873
seq_region_name: 17
source: dbSNP
start: 73352351
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352352
feature_type: variation
id: rs1457632478
seq_region_name: 17
source: dbSNP
start: 73352352
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352357
feature_type: variation
id: rs1158051982
seq_region_name: 17
source: dbSNP
start: 73352357
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352358
feature_type: variation
id: rs569149146
seq_region_name: 17
source: dbSNP
start: 73352358
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352359
feature_type: variation
id: rs2062546015
seq_region_name: 17
source: dbSNP
start: 73352359
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352362
feature_type: variation
id: rs1472468080
seq_region_name: 17
source: dbSNP
start: 73352362
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352363
feature_type: variation
id: rs539631135
seq_region_name: 17
source: dbSNP
start: 73352363
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352364
feature_type: variation
id: rs2062546096
seq_region_name: 17
source: dbSNP
start: 73352364
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352365
feature_type: variation
id: rs2145399927
seq_region_name: 17
source: dbSNP
start: 73352365
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352366
feature_type: variation
id: rs1185604318
seq_region_name: 17
source: dbSNP
start: 73352366
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352368
feature_type: variation
id: rs965567760
seq_region_name: 17
source: dbSNP
start: 73352368
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352370
feature_type: variation
id: rs1447866918
seq_region_name: 17
source: dbSNP
start: 73352370
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352372
feature_type: variation
id: rs936622958
seq_region_name: 17
source: dbSNP
start: 73352372
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352373
feature_type: variation
id: rs2145399957
seq_region_name: 17
source: dbSNP
start: 73352373
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352376
feature_type: variation
id: rs2062546226
seq_region_name: 17
source: dbSNP
start: 73352376
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352378
feature_type: variation
id: rs2062546252
seq_region_name: 17
source: dbSNP
start: 73352378
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352381
feature_type: variation
id: rs2062546286
seq_region_name: 17
source: dbSNP
start: 73352381
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352382
feature_type: variation
id: rs557859613
seq_region_name: 17
source: dbSNP
start: 73352382
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352391
feature_type: variation
id: rs2145399991
seq_region_name: 17
source: dbSNP
start: 73352391
strand: 1
-
alleles:
- CTCCTCCT
- CTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352399
feature_type: variation
id: rs142335113
seq_region_name: 17
source: dbSNP
start: 73352392
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352402
feature_type: variation
id: rs976232621
seq_region_name: 17
source: dbSNP
start: 73352402
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352403
feature_type: variation
id: rs2062546415
seq_region_name: 17
source: dbSNP
start: 73352403
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352404
feature_type: variation
id: rs1209774960
seq_region_name: 17
source: dbSNP
start: 73352404
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352406
feature_type: variation
id: rs2062546440
seq_region_name: 17
source: dbSNP
start: 73352406
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352408
feature_type: variation
id: rs942570062
seq_region_name: 17
source: dbSNP
start: 73352408
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352409
feature_type: variation
id: rs919035301
seq_region_name: 17
source: dbSNP
start: 73352409
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352410
feature_type: variation
id: rs2062546526
seq_region_name: 17
source: dbSNP
start: 73352410
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352412
feature_type: variation
id: rs1568361981
seq_region_name: 17
source: dbSNP
start: 73352412
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352414
feature_type: variation
id: rs2062546576
seq_region_name: 17
source: dbSNP
start: 73352414
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352420
feature_type: variation
id: rs2062546592
seq_region_name: 17
source: dbSNP
start: 73352420
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352423
feature_type: variation
id: rs1257806335
seq_region_name: 17
source: dbSNP
start: 73352423
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352428
feature_type: variation
id: rs1041262768
seq_region_name: 17
source: dbSNP
start: 73352428
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352429
feature_type: variation
id: rs1388850083
seq_region_name: 17
source: dbSNP
start: 73352429
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352430
feature_type: variation
id: rs2062546707
seq_region_name: 17
source: dbSNP
start: 73352430
strand: 1
-
alleles:
- CTGCTGTGGGGCTCCCCCACTCCCT
- CTGCTGTGGGGCTCCCCCACTCCCTGCTGTGGGGCTCCCCCACTCCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352454
feature_type: variation
id: rs751124832
seq_region_name: 17
source: dbSNP
start: 73352430
strand: 1
-
alleles:
- CTGCTGTGGGGCTCCCCCACTCCCTCAGCCCCCAGGCC
- CTGCTGTGGGGCTCCCCCACTCCCTCAGCCCCCAGGCCCTGCTGTGGGGCTCCCCCACTCCCTCAGCCCCCAGGCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73352467
feature_type: variation
id: rs2062546748
seq_region_name: 17
source: dbSNP
start: 73352430
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352436
feature_type: variation
id: rs2145400102
seq_region_name: 17
source: dbSNP
start: 73352436
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352441
feature_type: variation
id: rs767602704
seq_region_name: 17
source: dbSNP
start: 73352441
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352443
feature_type: variation
id: rs752872759
seq_region_name: 17
source: dbSNP
start: 73352443
strand: 1
-
alleles:
- CCCCC
- CCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352447
feature_type: variation
id: rs35218144
seq_region_name: 17
source: dbSNP
start: 73352443
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352444
feature_type: variation
id: rs367557009
seq_region_name: 17
source: dbSNP
start: 73352444
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352445
feature_type: variation
id: rs1247583873
seq_region_name: 17
source: dbSNP
start: 73352445
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352447
feature_type: variation
id: rs370202582
seq_region_name: 17
source: dbSNP
start: 73352447
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352448
feature_type: variation
id: rs984489076
seq_region_name: 17
source: dbSNP
start: 73352448
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352451
feature_type: variation
id: rs1303835883
seq_region_name: 17
source: dbSNP
start: 73352451
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352453
feature_type: variation
id: rs752330801
seq_region_name: 17
source: dbSNP
start: 73352453
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352456
feature_type: variation
id: rs1321461149
seq_region_name: 17
source: dbSNP
start: 73352456
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352458
feature_type: variation
id: rs1394570948
seq_region_name: 17
source: dbSNP
start: 73352458
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352461
feature_type: variation
id: rs779220046
seq_region_name: 17
source: dbSNP
start: 73352461
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73352466
feature_type: variation
id: rs1366023213
seq_region_name: 17
source: dbSNP
start: 73352466
strand: 1
-
alleles:
- CCGGTACC
- CCGGTACCGGTACC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73352473
feature_type: variation
id: rs2062547088
seq_region_name: 17
source: dbSNP
start: 73352466
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73352467
feature_type: variation
id: rs757337230
seq_region_name: 17
source: dbSNP
start: 73352467
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73352468
feature_type: variation
id: rs909111033
seq_region_name: 17
source: dbSNP
start: 73352468
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73352469
feature_type: variation
id: rs1599474765
seq_region_name: 17
source: dbSNP
start: 73352468
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73352469
feature_type: variation
id: rs1341427015
seq_region_name: 17
source: dbSNP
start: 73352469
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73352470
feature_type: variation
id: rs1233661842
seq_region_name: 17
source: dbSNP
start: 73352470
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73352472
feature_type: variation
id: rs1257613629
seq_region_name: 17
source: dbSNP
start: 73352472
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352473
feature_type: variation
id: rs1482063204
seq_region_name: 17
source: dbSNP
start: 73352473
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352475
feature_type: variation
id: rs779681558
seq_region_name: 17
source: dbSNP
start: 73352475
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352477
feature_type: variation
id: rs2062547301
seq_region_name: 17
source: dbSNP
start: 73352477
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73352479
feature_type: variation
id: rs540680710
seq_region_name: 17
source: dbSNP
start: 73352479
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352483
feature_type: variation
id: rs555480208
seq_region_name: 17
source: dbSNP
start: 73352483
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352486
feature_type: variation
id: rs1189471983
seq_region_name: 17
source: dbSNP
start: 73352486
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352491
feature_type: variation
id: rs1186181136
seq_region_name: 17
source: dbSNP
start: 73352491
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352492
feature_type: variation
id: rs937935545
seq_region_name: 17
source: dbSNP
start: 73352492
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352495
feature_type: variation
id: rs2062547582
seq_region_name: 17
source: dbSNP
start: 73352495
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352498
feature_type: variation
id: rs776415249
seq_region_name: 17
source: dbSNP
start: 73352498
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352502
feature_type: variation
id: rs1476556516
seq_region_name: 17
source: dbSNP
start: 73352502
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352503
feature_type: variation
id: rs1599474834
seq_region_name: 17
source: dbSNP
start: 73352503
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352506
feature_type: variation
id: rs761451844
seq_region_name: 17
source: dbSNP
start: 73352506
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73352507
feature_type: variation
id: rs373715499
seq_region_name: 17
source: dbSNP
start: 73352507
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352510
feature_type: variation
id: rs2145400341
seq_region_name: 17
source: dbSNP
start: 73352510
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352511
feature_type: variation
id: rs1599474848
seq_region_name: 17
source: dbSNP
start: 73352511
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352513
feature_type: variation
id: rs2145400353
seq_region_name: 17
source: dbSNP
start: 73352513
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352514
feature_type: variation
id: rs1046773682
seq_region_name: 17
source: dbSNP
start: 73352514
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352518
feature_type: variation
id: rs772978916
seq_region_name: 17
source: dbSNP
start: 73352518
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352519
feature_type: variation
id: rs780134066
seq_region_name: 17
source: dbSNP
start: 73352519
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352520
feature_type: variation
id: rs2062547884
seq_region_name: 17
source: dbSNP
start: 73352520
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352521
feature_type: variation
id: rs1224052915
seq_region_name: 17
source: dbSNP
start: 73352521
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352524
feature_type: variation
id: rs1054851364
seq_region_name: 17
source: dbSNP
start: 73352524
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352525
feature_type: variation
id: rs112644023
seq_region_name: 17
source: dbSNP
start: 73352525
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352526
feature_type: variation
id: rs375433539
seq_region_name: 17
source: dbSNP
start: 73352526
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352527
feature_type: variation
id: rs2062548039
seq_region_name: 17
source: dbSNP
start: 73352527
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352528
feature_type: variation
id: rs752748221
seq_region_name: 17
source: dbSNP
start: 73352528
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352531
feature_type: variation
id: rs1318664205
seq_region_name: 17
source: dbSNP
start: 73352531
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352534
feature_type: variation
id: rs1191521349
seq_region_name: 17
source: dbSNP
start: 73352534
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352536
feature_type: variation
id: rs764294571
seq_region_name: 17
source: dbSNP
start: 73352536
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352537
feature_type: variation
id: rs1361559416
seq_region_name: 17
source: dbSNP
start: 73352537
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352540
feature_type: variation
id: rs949287872
seq_region_name: 17
source: dbSNP
start: 73352540
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352543
feature_type: variation
id: rs754096472
seq_region_name: 17
source: dbSNP
start: 73352543
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352544
feature_type: variation
id: rs2062548296
seq_region_name: 17
source: dbSNP
start: 73352544
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352550
feature_type: variation
id: rs1303061948
seq_region_name: 17
source: dbSNP
start: 73352550
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352551
feature_type: variation
id: rs142293180
seq_region_name: 17
source: dbSNP
start: 73352551
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352552
feature_type: variation
id: rs573974183
seq_region_name: 17
source: dbSNP
start: 73352552
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352553
feature_type: variation
id: rs780763384
seq_region_name: 17
source: dbSNP
start: 73352553
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352555
feature_type: variation
id: rs189560899
seq_region_name: 17
source: dbSNP
start: 73352555
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352556
feature_type: variation
id: rs569708798
seq_region_name: 17
source: dbSNP
start: 73352556
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352561
feature_type: variation
id: rs562752695
seq_region_name: 17
source: dbSNP
start: 73352561
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352564
feature_type: variation
id: rs747854779
seq_region_name: 17
source: dbSNP
start: 73352564
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352570
feature_type: variation
id: rs1032346718
seq_region_name: 17
source: dbSNP
start: 73352570
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352572
feature_type: variation
id: rs200966106
seq_region_name: 17
source: dbSNP
start: 73352572
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352574
feature_type: variation
id: rs2062548650
seq_region_name: 17
source: dbSNP
start: 73352574
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352579
feature_type: variation
id: rs150849724
seq_region_name: 17
source: dbSNP
start: 73352579
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352580
feature_type: variation
id: rs770844185
seq_region_name: 17
source: dbSNP
start: 73352580
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352586
feature_type: variation
id: rs2062548780
seq_region_name: 17
source: dbSNP
start: 73352586
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352588
feature_type: variation
id: rs2062548812
seq_region_name: 17
source: dbSNP
start: 73352588
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73352589
feature_type: variation
id: rs1007137800
seq_region_name: 17
source: dbSNP
start: 73352589
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352590
feature_type: variation
id: rs2145400620
seq_region_name: 17
source: dbSNP
start: 73352590
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352593
feature_type: variation
id: rs2062548874
seq_region_name: 17
source: dbSNP
start: 73352593
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352594
feature_type: variation
id: rs1172353927
seq_region_name: 17
source: dbSNP
start: 73352594
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352598
feature_type: variation
id: rs371504437
seq_region_name: 17
source: dbSNP
start: 73352598
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352599
feature_type: variation
id: rs866286253
seq_region_name: 17
source: dbSNP
start: 73352599
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352600
feature_type: variation
id: rs764248419
seq_region_name: 17
source: dbSNP
start: 73352600
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352602
feature_type: variation
id: rs753957711
seq_region_name: 17
source: dbSNP
start: 73352602
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352603
feature_type: variation
id: rs2062549074
seq_region_name: 17
source: dbSNP
start: 73352603
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352606
feature_type: variation
id: rs2062549101
seq_region_name: 17
source: dbSNP
start: 73352606
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352610
feature_type: variation
id: rs1019914501
seq_region_name: 17
source: dbSNP
start: 73352610
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352611
feature_type: variation
id: rs762064426
seq_region_name: 17
source: dbSNP
start: 73352611
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352613
feature_type: variation
id: rs2062549172
seq_region_name: 17
source: dbSNP
start: 73352613
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352615
feature_type: variation
id: rs139282907
seq_region_name: 17
source: dbSNP
start: 73352615
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352617
feature_type: variation
id: rs750802289
seq_region_name: 17
source: dbSNP
start: 73352617
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352618
feature_type: variation
id: rs2062549234
seq_region_name: 17
source: dbSNP
start: 73352618
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352620
feature_type: variation
id: rs758897122
seq_region_name: 17
source: dbSNP
start: 73352620
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73352625
feature_type: variation
id: rs2062549304
seq_region_name: 17
source: dbSNP
start: 73352625
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73352627
feature_type: variation
id: rs1288824521
seq_region_name: 17
source: dbSNP
start: 73352627
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352631
feature_type: variation
id: rs780638775
seq_region_name: 17
source: dbSNP
start: 73352631
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352633
feature_type: variation
id: rs2062549387
seq_region_name: 17
source: dbSNP
start: 73352633
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73352634
feature_type: variation
id: rs35562089
seq_region_name: 17
source: dbSNP
start: 73352634
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352635
feature_type: variation
id: rs752122954
seq_region_name: 17
source: dbSNP
start: 73352635
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73352636
feature_type: variation
id: rs768549467
seq_region_name: 17
source: dbSNP
start: 73352636
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73352641
feature_type: variation
id: rs138870611
seq_region_name: 17
source: dbSNP
start: 73352641
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73352642
feature_type: variation
id: rs371671236
seq_region_name: 17
source: dbSNP
start: 73352642
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73352644
feature_type: variation
id: rs199515214
seq_region_name: 17
source: dbSNP
start: 73352644
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73352646
feature_type: variation
id: rs201219749
seq_region_name: 17
source: dbSNP
start: 73352646
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73352647
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73352823
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73352844
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73352861
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73352862
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73352881
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73352884
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73352889
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73352890
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73352893
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73352894
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73352900
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1599475331
seq_region_name: 17
source: dbSNP
start: 73352901
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73352907
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73352907
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73353144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353145
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353146
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353147
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353152
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353158
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353160
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353162
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs911336773
seq_region_name: 17
source: dbSNP
start: 73353164
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353165
feature_type: variation
id: rs866566964
seq_region_name: 17
source: dbSNP
start: 73353165
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353169
feature_type: variation
id: rs1390382813
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062553909
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062553957
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1041086719
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1350863643
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs556567238
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1481366915
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs901384768
seq_region_name: 17
source: dbSNP
start: 73353207
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1052615930
seq_region_name: 17
source: dbSNP
start: 73353208
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs994440488
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs578009016
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1047800232
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1018339605
seq_region_name: 17
source: dbSNP
start: 73353225
strand: 1
-
alleles:
- CAAGGAATTAGCAC
- CAAGGAATTAGCACAAGGAATTAGCAC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1483099016
seq_region_name: 17
source: dbSNP
start: 73353225
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1187216672
seq_region_name: 17
source: dbSNP
start: 73353228
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs964428069
seq_region_name: 17
source: dbSNP
start: 73353241
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062554328
seq_region_name: 17
source: dbSNP
start: 73353243
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs998197499
seq_region_name: 17
source: dbSNP
start: 73353244
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145402319
seq_region_name: 17
source: dbSNP
start: 73353246
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs765258276
seq_region_name: 17
source: dbSNP
start: 73353256
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145402337
seq_region_name: 17
source: dbSNP
start: 73353259
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353260
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062554438
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1426109867
seq_region_name: 17
source: dbSNP
start: 73353272
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353273
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1005698748
seq_region_name: 17
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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id: rs1599475629
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353294
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353296
strand: 1
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alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062554739
seq_region_name: 17
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start: 73353297
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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feature_type: variation
id: rs2062554777
seq_region_name: 17
source: dbSNP
start: 73353298
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353301
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73353302
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1393950906
seq_region_name: 17
source: dbSNP
start: 73353305
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1404965055
seq_region_name: 17
source: dbSNP
start: 73353313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs959129205
seq_region_name: 17
source: dbSNP
start: 73353314
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353315
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1024649826
seq_region_name: 17
source: dbSNP
start: 73353318
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353319
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353322
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs750680151
seq_region_name: 17
source: dbSNP
start: 73353323
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1456544452
seq_region_name: 17
source: dbSNP
start: 73353325
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs970833824
seq_region_name: 17
source: dbSNP
start: 73353326
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062555163
seq_region_name: 17
source: dbSNP
start: 73353330
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1365623549
seq_region_name: 17
source: dbSNP
start: 73353331
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062555227
seq_region_name: 17
source: dbSNP
start: 73353332
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353333
feature_type: variation
id: rs1185569102
seq_region_name: 17
source: dbSNP
start: 73353333
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145402590
seq_region_name: 17
source: dbSNP
start: 73353339
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353340
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1444202859
seq_region_name: 17
source: dbSNP
start: 73353342
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1244044966
seq_region_name: 17
source: dbSNP
start: 73353349
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs74789090
seq_region_name: 17
source: dbSNP
start: 73353357
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062555392
seq_region_name: 17
source: dbSNP
start: 73353359
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs978032211
seq_region_name: 17
source: dbSNP
start: 73353360
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353361
feature_type: variation
id: rs2062555455
seq_region_name: 17
source: dbSNP
start: 73353361
strand: 1
-
alleles:
- CCTTTCCT
- CCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353368
feature_type: variation
id: rs1568362397
seq_region_name: 17
source: dbSNP
start: 73353361
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353362
feature_type: variation
id: rs991232310
seq_region_name: 17
source: dbSNP
start: 73353362
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1284104667
seq_region_name: 17
source: dbSNP
start: 73353365
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353369
feature_type: variation
id: rs2062555600
seq_region_name: 17
source: dbSNP
start: 73353369
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353370
feature_type: variation
id: rs923875207
seq_region_name: 17
source: dbSNP
start: 73353370
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353374
feature_type: variation
id: rs2062555679
seq_region_name: 17
source: dbSNP
start: 73353374
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353377
feature_type: variation
id: rs560394632
seq_region_name: 17
source: dbSNP
start: 73353377
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353378
feature_type: variation
id: rs957880983
seq_region_name: 17
source: dbSNP
start: 73353378
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353382
feature_type: variation
id: rs989324678
seq_region_name: 17
source: dbSNP
start: 73353382
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353383
feature_type: variation
id: rs2062555811
seq_region_name: 17
source: dbSNP
start: 73353383
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353384
feature_type: variation
id: rs529655992
seq_region_name: 17
source: dbSNP
start: 73353384
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353385
feature_type: variation
id: rs2062555877
seq_region_name: 17
source: dbSNP
start: 73353385
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353388
feature_type: variation
id: rs1242036785
seq_region_name: 17
source: dbSNP
start: 73353388
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353392
feature_type: variation
id: rs949777348
seq_region_name: 17
source: dbSNP
start: 73353392
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353398
feature_type: variation
id: rs2062555958
seq_region_name: 17
source: dbSNP
start: 73353398
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353410
feature_type: variation
id: rs1315380836
seq_region_name: 17
source: dbSNP
start: 73353410
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353411
feature_type: variation
id: rs911284374
seq_region_name: 17
source: dbSNP
start: 73353411
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353412
feature_type: variation
id: rs1454327839
seq_region_name: 17
source: dbSNP
start: 73353412
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353413
feature_type: variation
id: rs1045387408
seq_region_name: 17
source: dbSNP
start: 73353413
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353416
feature_type: variation
id: rs1317490184
seq_region_name: 17
source: dbSNP
start: 73353416
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353418
feature_type: variation
id: rs2062556084
seq_region_name: 17
source: dbSNP
start: 73353418
strand: 1
-
alleles:
- TCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353423
feature_type: variation
id: rs1401192179
seq_region_name: 17
source: dbSNP
start: 73353421
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353423
feature_type: variation
id: rs1161530499
seq_region_name: 17
source: dbSNP
start: 73353423
strand: 1
-
alleles:
- TTTTTT
- TTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353428
feature_type: variation
id: rs924241088
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source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353524
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353541
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353546
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353553
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353556
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73353560
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353562
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353563
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353565
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353570
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353587
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353588
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599475944
seq_region_name: 17
source: dbSNP
start: 73353588
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568362475
seq_region_name: 17
source: dbSNP
start: 73353596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353597
feature_type: variation
id: rs1599475950
seq_region_name: 17
source: dbSNP
start: 73353597
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73353599
feature_type: variation
id: rs2062558381
seq_region_name: 17
source: dbSNP
start: 73353599
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2881284
seq_region_name: 17
source: dbSNP
start: 73353607
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353618
feature_type: variation
id: rs922702372
seq_region_name: 17
source: dbSNP
start: 73353618
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353619
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353619
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353622
feature_type: variation
id: rs1664506021
seq_region_name: 17
source: dbSNP
start: 73353622
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353624
feature_type: variation
id: rs2062558514
seq_region_name: 17
source: dbSNP
start: 73353624
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353625
feature_type: variation
id: rs983202141
seq_region_name: 17
source: dbSNP
start: 73353625
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353626
feature_type: variation
id: rs910112921
seq_region_name: 17
source: dbSNP
start: 73353626
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353627
feature_type: variation
id: rs2062558586
seq_region_name: 17
source: dbSNP
start: 73353627
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353633
feature_type: variation
id: rs2062558605
seq_region_name: 17
source: dbSNP
start: 73353633
strand: 1
-
alleles:
- AG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353634
feature_type: variation
id: rs2062558623
seq_region_name: 17
source: dbSNP
start: 73353633
strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353703
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353704
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353707
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73353712
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1051578036
seq_region_name: 17
source: dbSNP
start: 73353714
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062559739
seq_region_name: 17
source: dbSNP
start: 73353714
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73353720
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353720
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353720
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062559840
seq_region_name: 17
source: dbSNP
start: 73353721
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353722
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1264859584
seq_region_name: 17
source: dbSNP
start: 73353722
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1271485976
seq_region_name: 17
source: dbSNP
start: 73353722
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353723
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73353723
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1199337937
seq_region_name: 17
source: dbSNP
start: 73353724
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599476108
seq_region_name: 17
source: dbSNP
start: 73353729
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062560012
seq_region_name: 17
source: dbSNP
start: 73353731
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062560033
seq_region_name: 17
source: dbSNP
start: 73353732
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353733
feature_type: variation
id: rs2062560062
seq_region_name: 17
source: dbSNP
start: 73353733
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353734
feature_type: variation
id: rs1285006628
seq_region_name: 17
source: dbSNP
start: 73353734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353735
feature_type: variation
id: rs1599476115
seq_region_name: 17
source: dbSNP
start: 73353735
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353737
feature_type: variation
id: rs1225599723
seq_region_name: 17
source: dbSNP
start: 73353737
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs534387542
seq_region_name: 17
source: dbSNP
start: 73353738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353744
feature_type: variation
id: rs1380834669
seq_region_name: 17
source: dbSNP
start: 73353744
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353749
feature_type: variation
id: rs887142928
seq_region_name: 17
source: dbSNP
start: 73353749
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062560227
seq_region_name: 17
source: dbSNP
start: 73353752
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353757
feature_type: variation
id: rs1599476134
seq_region_name: 17
source: dbSNP
start: 73353757
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353758
feature_type: variation
id: rs1231692915
seq_region_name: 17
source: dbSNP
start: 73353758
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353761
feature_type: variation
id: rs1385475757
seq_region_name: 17
source: dbSNP
start: 73353761
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353765
feature_type: variation
id: rs2062560333
seq_region_name: 17
source: dbSNP
start: 73353765
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1004166251
seq_region_name: 17
source: dbSNP
start: 73353766
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353770
feature_type: variation
id: rs1453649518
seq_region_name: 17
source: dbSNP
start: 73353770
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353777
feature_type: variation
id: rs2346016
seq_region_name: 17
source: dbSNP
start: 73353777
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353789
feature_type: variation
id: rs567766930
seq_region_name: 17
source: dbSNP
start: 73353789
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353790
feature_type: variation
id: rs1159191661
seq_region_name: 17
source: dbSNP
start: 73353790
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353791
feature_type: variation
id: rs898404682
seq_region_name: 17
source: dbSNP
start: 73353791
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353794
feature_type: variation
id: rs181838472
seq_region_name: 17
source: dbSNP
start: 73353794
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353797
feature_type: variation
id: rs1162546515
seq_region_name: 17
source: dbSNP
start: 73353797
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353798
feature_type: variation
id: rs2062560762
seq_region_name: 17
source: dbSNP
start: 73353798
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353799
feature_type: variation
id: rs2145403880
seq_region_name: 17
source: dbSNP
start: 73353799
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353802
feature_type: variation
id: rs1046132418
seq_region_name: 17
source: dbSNP
start: 73353802
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353805
feature_type: variation
id: rs528259440
seq_region_name: 17
source: dbSNP
start: 73353805
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353808
feature_type: variation
id: rs1184599397
seq_region_name: 17
source: dbSNP
start: 73353808
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73353815
feature_type: variation
id: rs2062560920
seq_region_name: 17
source: dbSNP
start: 73353815
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354000
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73354004
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354009
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73354012
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354013
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354016
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354017
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354018
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73354020
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73354021
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354022
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354027
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354030
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1046337303
seq_region_name: 17
source: dbSNP
start: 73354031
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs906242047
seq_region_name: 17
source: dbSNP
start: 73354032
strand: 1
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354120
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73354129
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354144
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73354153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354155
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354162
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354164
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354171
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354174
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354180
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354182
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354184
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354185
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs560814248
seq_region_name: 17
source: dbSNP
start: 73354191
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs117711775
seq_region_name: 17
source: dbSNP
start: 73354196
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354197
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354198
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354199
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062566038
seq_region_name: 17
source: dbSNP
start: 73354202
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1183038275
seq_region_name: 17
source: dbSNP
start: 73354204
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354205
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354211
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354213
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354221
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354225
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1244103513
seq_region_name: 17
source: dbSNP
start: 73354230
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354233
feature_type: variation
id: rs1190097661
seq_region_name: 17
source: dbSNP
start: 73354233
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354234
feature_type: variation
id: rs1422871558
seq_region_name: 17
source: dbSNP
start: 73354234
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354241
feature_type: variation
id: rs1599476695
seq_region_name: 17
source: dbSNP
start: 73354241
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354244
feature_type: variation
id: rs778782899
seq_region_name: 17
source: dbSNP
start: 73354244
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354253
feature_type: variation
id: rs1389810389
seq_region_name: 17
source: dbSNP
start: 73354253
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354254
feature_type: variation
id: rs191190109
seq_region_name: 17
source: dbSNP
start: 73354254
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599476710
seq_region_name: 17
source: dbSNP
start: 73354256
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354260
feature_type: variation
id: rs2062566408
seq_region_name: 17
source: dbSNP
start: 73354260
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs955589439
seq_region_name: 17
source: dbSNP
start: 73354261
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062566450
seq_region_name: 17
source: dbSNP
start: 73354265
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354267
feature_type: variation
id: rs1353806093
seq_region_name: 17
source: dbSNP
start: 73354267
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354275
feature_type: variation
id: rs1052597932
seq_region_name: 17
source: dbSNP
start: 73354275
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354277
feature_type: variation
id: rs2062566519
seq_region_name: 17
source: dbSNP
start: 73354277
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354278
feature_type: variation
id: rs549568779
seq_region_name: 17
source: dbSNP
start: 73354278
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354280
feature_type: variation
id: rs2062566561
seq_region_name: 17
source: dbSNP
start: 73354280
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73354282
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354288
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
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feature_type: variation
id: rs2062566691
seq_region_name: 17
source: dbSNP
start: 73354295
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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feature_type: variation
id: rs2062566712
seq_region_name: 17
source: dbSNP
start: 73354296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs899712933
seq_region_name: 17
source: dbSNP
start: 73354301
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354303
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062566792
seq_region_name: 17
source: dbSNP
start: 73354309
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
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id: rs531847652
seq_region_name: 17
source: dbSNP
start: 73354313
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs1568362715
seq_region_name: 17
source: dbSNP
start: 73354314
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599476763
seq_region_name: 17
source: dbSNP
start: 73354315
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- CTCTGGGCCTTGCCCTCGTGGGACATAATTCACCTTCA
- "-"
assembly_name: GRCh38
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consequence_type: intron_variant
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id: rs1386170206
seq_region_name: 17
source: dbSNP
start: 73354320
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1372942864
seq_region_name: 17
source: dbSNP
start: 73354329
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354334
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1038377239
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354337
strand: 1
-
alleles:
- GGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354339
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- ATA
- ATATA
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354344
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1051059355
seq_region_name: 17
source: dbSNP
start: 73354346
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1206535025
seq_region_name: 17
source: dbSNP
start: 73354350
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354351
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354358
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354364
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354365
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354366
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs373061024
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354377
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354378
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs907097025
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source: dbSNP
start: 73354379
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354380
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs186187773
seq_region_name: 17
source: dbSNP
start: 73354385
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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id: rs554760818
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354391
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062567573
seq_region_name: 17
source: dbSNP
start: 73354392
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1413658534
seq_region_name: 17
source: dbSNP
start: 73354393
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs982100233
seq_region_name: 17
source: dbSNP
start: 73354397
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354401
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73354404
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354410
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs956393059
seq_region_name: 17
source: dbSNP
start: 73354412
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145405371
seq_region_name: 17
source: dbSNP
start: 73354416
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062567766
seq_region_name: 17
source: dbSNP
start: 73354422
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1246883357
seq_region_name: 17
source: dbSNP
start: 73354424
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354425
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062567831
seq_region_name: 17
source: dbSNP
start: 73354427
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1157327063
seq_region_name: 17
source: dbSNP
start: 73354436
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062567876
seq_region_name: 17
source: dbSNP
start: 73354439
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs373344835
seq_region_name: 17
source: dbSNP
start: 73354440
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354444
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867010465
seq_region_name: 17
source: dbSNP
start: 73354447
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145405440
seq_region_name: 17
source: dbSNP
start: 73354448
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062567964
seq_region_name: 17
source: dbSNP
start: 73354452
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062567983
seq_region_name: 17
source: dbSNP
start: 73354453
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354455
feature_type: variation
id: rs1407726621
seq_region_name: 17
source: dbSNP
start: 73354455
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062568025
seq_region_name: 17
source: dbSNP
start: 73354456
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354459
feature_type: variation
id: rs2062568051
seq_region_name: 17
source: dbSNP
start: 73354459
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354461
feature_type: variation
id: rs1255367647
seq_region_name: 17
source: dbSNP
start: 73354461
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1415546649
seq_region_name: 17
source: dbSNP
start: 73354472
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354473
feature_type: variation
id: rs59552028
seq_region_name: 17
source: dbSNP
start: 73354473
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354475
feature_type: variation
id: rs1261191952
seq_region_name: 17
source: dbSNP
start: 73354475
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062568192
seq_region_name: 17
source: dbSNP
start: 73354476
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354478
feature_type: variation
id: rs2062568208
seq_region_name: 17
source: dbSNP
start: 73354478
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062568227
seq_region_name: 17
source: dbSNP
start: 73354482
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354487
feature_type: variation
id: rs2145405548
seq_region_name: 17
source: dbSNP
start: 73354487
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354493
feature_type: variation
id: rs1222910243
seq_region_name: 17
source: dbSNP
start: 73354493
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354494
feature_type: variation
id: rs576455613
seq_region_name: 17
source: dbSNP
start: 73354494
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354495
feature_type: variation
id: rs541043554
seq_region_name: 17
source: dbSNP
start: 73354495
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062568343
seq_region_name: 17
source: dbSNP
start: 73354496
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354503
feature_type: variation
id: rs147586487
seq_region_name: 17
source: dbSNP
start: 73354503
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354506
feature_type: variation
id: rs1414290224
seq_region_name: 17
source: dbSNP
start: 73354506
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354507
feature_type: variation
id: rs527996340
seq_region_name: 17
source: dbSNP
start: 73354507
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354509
feature_type: variation
id: rs542904174
seq_region_name: 17
source: dbSNP
start: 73354509
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354510
feature_type: variation
id: rs1335442546
seq_region_name: 17
source: dbSNP
start: 73354510
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354512
feature_type: variation
id: rs2062568472
seq_region_name: 17
source: dbSNP
start: 73354512
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354513
feature_type: variation
id: rs975042865
seq_region_name: 17
source: dbSNP
start: 73354513
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354514
feature_type: variation
id: rs2062568514
seq_region_name: 17
source: dbSNP
start: 73354514
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354516
feature_type: variation
id: rs2062568538
seq_region_name: 17
source: dbSNP
start: 73354516
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354678
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354680
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354694
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354700
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354705
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73354706
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354708
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354720
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354721
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354723
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354724
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599477231
seq_region_name: 17
source: dbSNP
start: 73354727
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599477235
seq_region_name: 17
source: dbSNP
start: 73354730
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73354732
feature_type: variation
id: rs1772492064
seq_region_name: 17
source: dbSNP
start: 73354732
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73354738
feature_type: variation
id: rs1381898963
seq_region_name: 17
source: dbSNP
start: 73354738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354742
feature_type: variation
id: rs1408216724
seq_region_name: 17
source: dbSNP
start: 73354742
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354744
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id: rs368927373
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73354871
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354872
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354878
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354881
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354883
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs955153928
seq_region_name: 17
source: dbSNP
start: 73354887
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73354892
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73354894
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354895
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062573498
seq_region_name: 17
source: dbSNP
start: 73354896
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145406609
seq_region_name: 17
source: dbSNP
start: 73354898
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2145406611
seq_region_name: 17
source: dbSNP
start: 73354905
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354909
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354910
feature_type: variation
id: rs1435714432
seq_region_name: 17
source: dbSNP
start: 73354910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062573580
seq_region_name: 17
source: dbSNP
start: 73354912
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354913
feature_type: variation
id: rs2062573606
seq_region_name: 17
source: dbSNP
start: 73354913
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354915
feature_type: variation
id: rs750534488
seq_region_name: 17
source: dbSNP
start: 73354915
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354916
feature_type: variation
id: rs754904744
seq_region_name: 17
source: dbSNP
start: 73354916
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs778979157
seq_region_name: 17
source: dbSNP
start: 73354918
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062573716
seq_region_name: 17
source: dbSNP
start: 73354919
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354924
feature_type: variation
id: rs1296239240
seq_region_name: 17
source: dbSNP
start: 73354924
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354925
feature_type: variation
id: rs973943679
seq_region_name: 17
source: dbSNP
start: 73354925
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354929
feature_type: variation
id: rs1226011536
seq_region_name: 17
source: dbSNP
start: 73354929
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354933
feature_type: variation
id: rs2062573887
seq_region_name: 17
source: dbSNP
start: 73354933
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354935
feature_type: variation
id: rs1464913504
seq_region_name: 17
source: dbSNP
start: 73354935
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73354939
feature_type: variation
id: rs2062573967
seq_region_name: 17
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs558299655
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354959
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73354962
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062574453
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1202356506
seq_region_name: 17
source: dbSNP
start: 73354968
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062574539
seq_region_name: 17
source: dbSNP
start: 73354973
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73354979
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599477554
seq_region_name: 17
source: dbSNP
start: 73354981
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062574653
seq_region_name: 17
source: dbSNP
start: 73354983
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1043299332
seq_region_name: 17
source: dbSNP
start: 73354987
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1323511804
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145406783
seq_region_name: 17
source: dbSNP
start: 73354991
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1250398786
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1254892944
seq_region_name: 17
source: dbSNP
start: 73354999
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1233429039
seq_region_name: 17
source: dbSNP
start: 73355001
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355003
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355004
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs900771099
seq_region_name: 17
source: dbSNP
start: 73355007
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062574879
seq_region_name: 17
source: dbSNP
start: 73355018
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs996306105
seq_region_name: 17
source: dbSNP
start: 73355019
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062574926
seq_region_name: 17
source: dbSNP
start: 73355025
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs183324532
seq_region_name: 17
source: dbSNP
start: 73355026
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs12938296
seq_region_name: 17
source: dbSNP
start: 73355028
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1007973683
seq_region_name: 17
source: dbSNP
start: 73355029
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1161742444
seq_region_name: 17
source: dbSNP
start: 73355040
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599477605
seq_region_name: 17
source: dbSNP
start: 73355046
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1393434593
seq_region_name: 17
source: dbSNP
start: 73355048
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1450328956
seq_region_name: 17
source: dbSNP
start: 73355052
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs897400667
seq_region_name: 17
source: dbSNP
start: 73355053
strand: 1
-
alleles:
- CCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1173229096
seq_region_name: 17
source: dbSNP
start: 73355057
strand: 1
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alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355058
feature_type: variation
id: rs1015784012
seq_region_name: 17
source: dbSNP
start: 73355058
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs961016925
seq_region_name: 17
source: dbSNP
start: 73355060
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs543346871
seq_region_name: 17
source: dbSNP
start: 73355061
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1440654926
seq_region_name: 17
source: dbSNP
start: 73355063
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs970214033
seq_region_name: 17
source: dbSNP
start: 73355068
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs919819451
seq_region_name: 17
source: dbSNP
start: 73355069
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs980604085
seq_region_name: 17
source: dbSNP
start: 73355075
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs969953124
seq_region_name: 17
source: dbSNP
start: 73355077
strand: 1
-
alleles:
- TT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1257490968
seq_region_name: 17
source: dbSNP
start: 73355080
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355081
feature_type: variation
id: rs1035773632
seq_region_name: 17
source: dbSNP
start: 73355081
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs980311089
seq_region_name: 17
source: dbSNP
start: 73355082
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355083
feature_type: variation
id: rs561550153
seq_region_name: 17
source: dbSNP
start: 73355083
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355084
feature_type: variation
id: rs12948429
seq_region_name: 17
source: dbSNP
start: 73355084
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355086
feature_type: variation
id: rs1354032807
seq_region_name: 17
source: dbSNP
start: 73355086
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1311164629
seq_region_name: 17
source: dbSNP
start: 73355091
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355092
feature_type: variation
id: rs2062575559
seq_region_name: 17
source: dbSNP
start: 73355092
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355093
feature_type: variation
id: rs1243583274
seq_region_name: 17
source: dbSNP
start: 73355093
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355094
feature_type: variation
id: rs367802120
seq_region_name: 17
source: dbSNP
start: 73355094
strand: 1
-
alleles:
- GGGG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355097
feature_type: variation
id: rs1312799669
seq_region_name: 17
source: dbSNP
start: 73355094
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355096
feature_type: variation
id: rs1242132519
seq_region_name: 17
source: dbSNP
start: 73355096
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355098
feature_type: variation
id: rs2145406997
seq_region_name: 17
source: dbSNP
start: 73355098
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355101
feature_type: variation
id: rs544054566
seq_region_name: 17
source: dbSNP
start: 73355101
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355105
feature_type: variation
id: rs565447359
seq_region_name: 17
source: dbSNP
start: 73355105
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355107
feature_type: variation
id: rs913330642
seq_region_name: 17
source: dbSNP
start: 73355107
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355108
feature_type: variation
id: rs947345323
seq_region_name: 17
source: dbSNP
start: 73355108
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355109
feature_type: variation
id: rs947302956
seq_region_name: 17
source: dbSNP
start: 73355109
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355113
feature_type: variation
id: rs2062575818
seq_region_name: 17
source: dbSNP
start: 73355113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355124
feature_type: variation
id: rs1270432719
seq_region_name: 17
source: dbSNP
start: 73355124
strand: 1
-
alleles:
- CTTACTT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355130
feature_type: variation
id: rs1161989593
seq_region_name: 17
source: dbSNP
start: 73355124
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355136
feature_type: variation
id: rs1485142467
seq_region_name: 17
source: dbSNP
start: 73355136
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355140
feature_type: variation
id: rs1043078194
seq_region_name: 17
source: dbSNP
start: 73355140
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355143
feature_type: variation
id: rs1599477749
seq_region_name: 17
source: dbSNP
start: 73355143
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355145
feature_type: variation
id: rs2062575924
seq_region_name: 17
source: dbSNP
start: 73355145
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355146
feature_type: variation
id: rs1205130312
seq_region_name: 17
source: dbSNP
start: 73355146
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355147
feature_type: variation
id: rs2062575968
seq_region_name: 17
source: dbSNP
start: 73355147
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355151
feature_type: variation
id: rs900721836
seq_region_name: 17
source: dbSNP
start: 73355151
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355152
feature_type: variation
id: rs2062576026
seq_region_name: 17
source: dbSNP
start: 73355152
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355154
feature_type: variation
id: rs1260378956
seq_region_name: 17
source: dbSNP
start: 73355154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355155
feature_type: variation
id: rs2062576078
seq_region_name: 17
source: dbSNP
start: 73355155
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355156
feature_type: variation
id: rs1599477771
seq_region_name: 17
source: dbSNP
start: 73355156
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355157
feature_type: variation
id: rs2062576128
seq_region_name: 17
source: dbSNP
start: 73355157
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355158
feature_type: variation
id: rs2062576145
seq_region_name: 17
source: dbSNP
start: 73355158
strand: 1
-
alleles:
- "-"
- AATATATATATATATATATATATATATATATATATA
- TATATATATATATATATATATATATATATA
- TATATATATATATATATATATATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355158
feature_type: variation
id: rs1444251376
seq_region_name: 17
source: dbSNP
start: 73355159
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355159
feature_type: variation
id: rs1301550701
seq_region_name: 17
source: dbSNP
start: 73355159
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355160
feature_type: variation
id: rs1751647445
seq_region_name: 17
source: dbSNP
start: 73355160
strand: 1
-
alleles:
- ATATATA
- ATATATACATATATATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355166
feature_type: variation
id: rs2062576214
seq_region_name: 17
source: dbSNP
start: 73355160
strand: 1
-
alleles:
- ATATATATAT
- ATATATATATGTATATATATAT
- ATATATATATGTATATATATATAT
- ATATATATATGTATATATATATATAT
- ATATATATATGTATATATATATATATAT
- ATATATATATGTATATATATATATATATATATATAT
- ATATATATATGTATATATATATATATATATATATATATATGTATATATATATATATAT
- ATATATATATGTATATATATATATATATATATATATATGTATATATATATATATAT
- ATATATATATGTATATATATATATATATATATATGTATATATATATAT
- ATATATATATGTATATATATATATATATATATATGTATATATATATATAT
- ATATATATATGTATATATATATATATATATATATGTATATATATATATATAT
- ATATATATATGTATATATATATATATATATATGTATATATATATAT
- ATATATATATGTATATATATATATATATATATGTATATATATATATAT
- ATATATATATGTATATATATATATATATATATGTATATATATATATATAT
- ATATATATATGTATATATATATATATATATATGTATATATATATATATATAT
- ATATATATATGTATATATATATATATATATATGTATATATATATATATATATAT
- ATATATATATGTATATATATATATATATATATGTGTATATATATATAT
- ATATATATATGTGTATATATATATATAT
- ATATATATATGTGTATATATATATATATATATGTATATATATATAT
- ATATATATATGTGTATATATATATATATATATGTATATATATATATAT
- ATATATATATGTGTATATATATATATATATATGTATATATATATATATAT
- ATATATATATTTATATATATATATATATATATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355169
feature_type: variation
id: rs1355689208
seq_region_name: 17
source: dbSNP
start: 73355160
strand: 1
-
alleles:
- ATATATATATATATAT
- ATATATAT
- ATATATATAT
- ATATATATATAT
- ATATATATATATAT
- ATATATATATATATATAT
- ATATATATATATATATATAT
- ATATATATATATATATATATAT
- ATATATATATATATATATATATACATATATATATATATATATATAT
- ATATATATATATATATATATATAT
- ATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATATATATATATAT
- ATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs1555750469
seq_region_name: 17
source: dbSNP
start: 73355160
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355161
feature_type: variation
id: rs2062576642
seq_region_name: 17
source: dbSNP
start: 73355161
strand: 1
-
alleles:
- TATATATAT
- TATATATATGTATATATATATATATATATATGTATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355169
feature_type: variation
id: rs1491097590
seq_region_name: 17
source: dbSNP
start: 73355161
strand: 1
-
alleles:
- TATATATATATATAT
- TATATATATATATATATATATATATATATATATCTATATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs2145407184
seq_region_name: 17
source: dbSNP
start: 73355161
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355162
feature_type: variation
id: rs2062576712
seq_region_name: 17
source: dbSNP
start: 73355162
strand: 1
-
alleles:
- A
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355162
feature_type: variation
id: rs2062576748
seq_region_name: 17
source: dbSNP
start: 73355162
strand: 1
-
alleles:
- ATATATATATAT
- ATATATATATATATATATATATATATATACATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs1417370502
seq_region_name: 17
source: dbSNP
start: 73355164
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355165
feature_type: variation
id: rs2062576839
seq_region_name: 17
source: dbSNP
start: 73355165
strand: 1
-
alleles:
- TATAT
- TATATGTATAT
- TATATGTATATATATATATATATATATGTATATATATATGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355169
feature_type: variation
id: rs1473054985
seq_region_name: 17
source: dbSNP
start: 73355165
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355166
feature_type: variation
id: rs2062576933
seq_region_name: 17
source: dbSNP
start: 73355166
strand: 1
-
alleles:
- ATATATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355174
feature_type: variation
id: rs559672703
seq_region_name: 17
source: dbSNP
start: 73355166
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355167
feature_type: variation
id: rs1423628287
seq_region_name: 17
source: dbSNP
start: 73355167
strand: 1
-
alleles:
- TATATATAT
- TATATATATATATATATATATATATATATATATGTATATATAT
- TATATATATATATATATATATATATCTATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs1161037415
seq_region_name: 17
source: dbSNP
start: 73355167
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355168
feature_type: variation
id: rs2062577084
seq_region_name: 17
source: dbSNP
start: 73355168
strand: 1
-
alleles:
- ATATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355174
feature_type: variation
id: rs2062577113
seq_region_name: 17
source: dbSNP
start: 73355168
strand: 1
-
alleles:
- T
- TGT
- TGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355169
feature_type: variation
id: rs1599477828
seq_region_name: 17
source: dbSNP
start: 73355169
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355170
feature_type: variation
id: rs111979464
seq_region_name: 17
source: dbSNP
start: 73355170
strand: 1
-
alleles:
- ATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355174
feature_type: variation
id: rs2062577273
seq_region_name: 17
source: dbSNP
start: 73355170
strand: 1
-
alleles:
- ATATAT
- ATATATATATATATATATATATATATATATAGATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs1409564437
seq_region_name: 17
source: dbSNP
start: 73355170
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355171
feature_type: variation
id: rs2062577306
seq_region_name: 17
source: dbSNP
start: 73355171
strand: 1
-
alleles:
- T
- TT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355171
feature_type: variation
id: rs2062577349
seq_region_name: 17
source: dbSNP
start: 73355171
strand: 1
-
alleles:
- TATAT
- TATATATATATATATATATATATATATATATATATATATTTATAT
- TATATATATATATATATATATATATATATCTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs2062577388
seq_region_name: 17
source: dbSNP
start: 73355171
strand: 1
-
alleles:
- TATATTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355177
feature_type: variation
id: rs2062577432
seq_region_name: 17
source: dbSNP
start: 73355171
strand: 1
-
alleles:
- TATATTTTTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355180
feature_type: variation
id: rs1477868627
seq_region_name: 17
source: dbSNP
start: 73355171
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355172
feature_type: variation
id: rs1257364403
seq_region_name: 17
source: dbSNP
start: 73355172
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355172
feature_type: variation
id: rs1264817542
seq_region_name: 17
source: dbSNP
start: 73355172
strand: 1
-
alleles:
- ATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355174
feature_type: variation
id: rs1196340992
seq_region_name: 17
source: dbSNP
start: 73355172
strand: 1
-
alleles:
- T
- TCTTTTTTTTT
- TT
- TTT
- TTTT
- TTTTTT
- TTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355173
feature_type: variation
id: rs1450719562
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TAT
- TATATATATATATATATATATATATATATTTAT
- TATATATATATATATGTAT
- TATATATATATATGTAT
- TATATATATATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs1555750484
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TATT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355176
feature_type: variation
id: rs2062577741
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TATTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355177
feature_type: variation
id: rs2062577759
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TATTTTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355179
feature_type: variation
id: rs1454890646
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TATTTTTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355180
feature_type: variation
id: rs1281502854
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TATTTTTTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355181
feature_type: variation
id: rs1568363041
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- TATTTTTTTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355182
feature_type: variation
id: rs1568363043
seq_region_name: 17
source: dbSNP
start: 73355173
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355174
feature_type: variation
id: rs1303406896
seq_region_name: 17
source: dbSNP
start: 73355174
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355174
feature_type: variation
id: rs1490625849
seq_region_name: 17
source: dbSNP
start: 73355174
strand: 1
-
alleles:
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355195
feature_type: variation
id: rs770032791
seq_region_name: 17
source: dbSNP
start: 73355175
strand: 1
-
alleles:
- "-"
- A
- ATA
- ATATA
- ATATACATATATA
- ATATATA
- ATATATATA
- ATATATATATA
- ATATATATATATA
- ATATATATATATATA
- ATATATATATATATATA
- ATATATATATATATATATA
- ATATATATATATATATATATA
- ATATATATATATATATATATATA
- ATATATATATATATATATATATATA
- ATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATGTATATATATATATATATACG
- ATATATATATGTA
- ATATATATGTA
- ATATATGTA
- ATATGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355175
feature_type: variation
id: rs1555750470
seq_region_name: 17
source: dbSNP
start: 73355176
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355176
feature_type: variation
id: rs1229372788
seq_region_name: 17
source: dbSNP
start: 73355176
strand: 1
-
alleles:
- "-"
- A
- ATA
- ATATA
- ATATATA
- ATATATATA
- ATATATATATA
- ATATATATATATA
- ATATATATATATATA
- ATATATATATATATATA
- ATATATATATATATATATA
- ATATATATATATATATATATA
- ATATATATATATATATATATATA
- ATATATATATATATATATATATATA
- ATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATA
- ATATATATATATATGTA
- ATATATATGTA
- ATATATGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355176
feature_type: variation
id: rs1568363071
seq_region_name: 17
source: dbSNP
start: 73355177
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355177
feature_type: variation
id: rs1403683199
seq_region_name: 17
source: dbSNP
start: 73355177
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355178
feature_type: variation
id: rs1393746335
seq_region_name: 17
source: dbSNP
start: 73355178
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355179
feature_type: variation
id: rs1311766843
seq_region_name: 17
source: dbSNP
start: 73355179
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355180
feature_type: variation
id: rs1350662596
seq_region_name: 17
source: dbSNP
start: 73355180
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355181
feature_type: variation
id: rs1229854879
seq_region_name: 17
source: dbSNP
start: 73355181
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355182
feature_type: variation
id: rs866728193
seq_region_name: 17
source: dbSNP
start: 73355182
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355183
feature_type: variation
id: rs1315568019
seq_region_name: 17
source: dbSNP
start: 73355183
strand: 1
-
alleles:
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTTTCTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355195
feature_type: variation
id: rs2062580544
seq_region_name: 17
source: dbSNP
start: 73355183
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355184
feature_type: variation
id: rs1393353517
seq_region_name: 17
source: dbSNP
start: 73355184
strand: 1
-
alleles:
- TTTT
- TTTTCTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355188
feature_type: variation
id: rs1415952656
seq_region_name: 17
source: dbSNP
start: 73355185
strand: 1
-
alleles:
- TTTTTTTTT
- TTTTTTTTTCTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355193
feature_type: variation
id: rs2062580637
seq_region_name: 17
source: dbSNP
start: 73355185
strand: 1
-
alleles:
- TTTTTTTTTTT
- TTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTCTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTCTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355195
feature_type: variation
id: rs1568363079
seq_region_name: 17
source: dbSNP
start: 73355185
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355186
feature_type: variation
id: rs1257141474
seq_region_name: 17
source: dbSNP
start: 73355186
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355188
feature_type: variation
id: rs1347790116
seq_region_name: 17
source: dbSNP
start: 73355188
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355192
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1483501515
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1184680631
seq_region_name: 17
source: dbSNP
start: 73355195
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355195
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355196
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355196
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1418326352
seq_region_name: 17
source: dbSNP
start: 73355197
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145407829
seq_region_name: 17
source: dbSNP
start: 73355198
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1176556439
seq_region_name: 17
source: dbSNP
start: 73355199
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1379244220
seq_region_name: 17
source: dbSNP
start: 73355200
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355201
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs111252423
seq_region_name: 17
source: dbSNP
start: 73355202
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1222856972
seq_region_name: 17
source: dbSNP
start: 73355203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599478077
seq_region_name: 17
source: dbSNP
start: 73355205
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062581560
seq_region_name: 17
source: dbSNP
start: 73355207
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062581585
seq_region_name: 17
source: dbSNP
start: 73355209
strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062581606
seq_region_name: 17
source: dbSNP
start: 73355209
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1464493107
seq_region_name: 17
source: dbSNP
start: 73355210
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568363104
seq_region_name: 17
source: dbSNP
start: 73355212
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355213
feature_type: variation
id: rs1256731959
seq_region_name: 17
source: dbSNP
start: 73355213
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1172399839
seq_region_name: 17
source: dbSNP
start: 73355215
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs371248723
seq_region_name: 17
source: dbSNP
start: 73355216
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs550338929
seq_region_name: 17
source: dbSNP
start: 73355217
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355220
feature_type: variation
id: rs1221238665
seq_region_name: 17
source: dbSNP
start: 73355220
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062581818
seq_region_name: 17
source: dbSNP
start: 73355222
strand: 1
-
alleles:
- GCTG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355225
feature_type: variation
id: rs1599478109
seq_region_name: 17
source: dbSNP
start: 73355222
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355223
feature_type: variation
id: rs2062581873
seq_region_name: 17
source: dbSNP
start: 73355223
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062581895
seq_region_name: 17
source: dbSNP
start: 73355227
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355229
feature_type: variation
id: rs2062581918
seq_region_name: 17
source: dbSNP
start: 73355229
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355231
feature_type: variation
id: rs2062581943
seq_region_name: 17
source: dbSNP
start: 73355231
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599478113
seq_region_name: 17
source: dbSNP
start: 73355235
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355237
feature_type: variation
id: rs2062581988
seq_region_name: 17
source: dbSNP
start: 73355237
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355238
feature_type: variation
id: rs2062582018
seq_region_name: 17
source: dbSNP
start: 73355238
strand: 1
-
alleles:
- ATGAT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062582042
seq_region_name: 17
source: dbSNP
start: 73355238
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355239
feature_type: variation
id: rs1365115939
seq_region_name: 17
source: dbSNP
start: 73355239
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1292723472
seq_region_name: 17
source: dbSNP
start: 73355245
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355246
feature_type: variation
id: rs1566293
seq_region_name: 17
source: dbSNP
start: 73355246
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1168487602
seq_region_name: 17
source: dbSNP
start: 73355251
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355254
feature_type: variation
id: rs1465080085
seq_region_name: 17
source: dbSNP
start: 73355254
strand: 1
-
alleles:
- CAACCTCC
- CAACCTCCAACCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355262
feature_type: variation
id: rs1424403798
seq_region_name: 17
source: dbSNP
start: 73355255
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355262
feature_type: variation
id: rs547529565
seq_region_name: 17
source: dbSNP
start: 73355262
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355263
feature_type: variation
id: rs1431653506
seq_region_name: 17
source: dbSNP
start: 73355263
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355264
feature_type: variation
id: rs978659863
seq_region_name: 17
source: dbSNP
start: 73355264
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355265
feature_type: variation
id: rs2062582313
seq_region_name: 17
source: dbSNP
start: 73355265
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355269
feature_type: variation
id: rs1391140952
seq_region_name: 17
source: dbSNP
start: 73355269
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355270
feature_type: variation
id: rs746624478
seq_region_name: 17
source: dbSNP
start: 73355270
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355271
feature_type: variation
id: rs2062582378
seq_region_name: 17
source: dbSNP
start: 73355271
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355273
feature_type: variation
id: rs2062582396
seq_region_name: 17
source: dbSNP
start: 73355273
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355275
feature_type: variation
id: rs1489683576
seq_region_name: 17
source: dbSNP
start: 73355275
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355276
feature_type: variation
id: rs1302440236
seq_region_name: 17
source: dbSNP
start: 73355276
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355278
feature_type: variation
id: rs2145408061
seq_region_name: 17
source: dbSNP
start: 73355278
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355282
feature_type: variation
id: rs2062582445
seq_region_name: 17
source: dbSNP
start: 73355282
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355283
feature_type: variation
id: rs921769194
seq_region_name: 17
source: dbSNP
start: 73355283
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355284
feature_type: variation
id: rs931825967
seq_region_name: 17
source: dbSNP
start: 73355284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355287
feature_type: variation
id: rs1258123137
seq_region_name: 17
source: dbSNP
start: 73355287
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355292
feature_type: variation
id: rs2062582551
seq_region_name: 17
source: dbSNP
start: 73355291
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355292
feature_type: variation
id: rs996434571
seq_region_name: 17
source: dbSNP
start: 73355292
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355296
feature_type: variation
id: rs1232749168
seq_region_name: 17
source: dbSNP
start: 73355296
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355299
feature_type: variation
id: rs559736281
seq_region_name: 17
source: dbSNP
start: 73355299
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355301
feature_type: variation
id: rs1343022287
seq_region_name: 17
source: dbSNP
start: 73355301
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355302
feature_type: variation
id: rs1219550640
seq_region_name: 17
source: dbSNP
start: 73355302
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355303
feature_type: variation
id: rs2062582700
seq_region_name: 17
source: dbSNP
start: 73355303
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355311
feature_type: variation
id: rs2062582724
seq_region_name: 17
source: dbSNP
start: 73355311
strand: 1
-
alleles:
- TATAGGCACCCGC
- TATAGGCACCCGCTATAGGCACCCGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355328
feature_type: variation
id: rs2062582747
seq_region_name: 17
source: dbSNP
start: 73355316
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355319
feature_type: variation
id: rs1207522142
seq_region_name: 17
source: dbSNP
start: 73355319
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355322
feature_type: variation
id: rs1249796953
seq_region_name: 17
source: dbSNP
start: 73355322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355326
feature_type: variation
id: rs1480440307
seq_region_name: 17
source: dbSNP
start: 73355326
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355327
feature_type: variation
id: rs2062582852
seq_region_name: 17
source: dbSNP
start: 73355327
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355331
feature_type: variation
id: rs763226745
seq_region_name: 17
source: dbSNP
start: 73355331
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355332
feature_type: variation
id: rs1568363150
seq_region_name: 17
source: dbSNP
start: 73355332
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355334
feature_type: variation
id: rs890609173
seq_region_name: 17
source: dbSNP
start: 73355334
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355335
feature_type: variation
id: rs530024214
seq_region_name: 17
source: dbSNP
start: 73355335
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355336
feature_type: variation
id: rs2145408183
seq_region_name: 17
source: dbSNP
start: 73355336
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355338
feature_type: variation
id: rs548489084
seq_region_name: 17
source: dbSNP
start: 73355338
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355339
feature_type: variation
id: rs961130553
seq_region_name: 17
source: dbSNP
start: 73355339
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355340
feature_type: variation
id: rs995095069
seq_region_name: 17
source: dbSNP
start: 73355340
strand: 1
-
alleles:
- TTATTTATTTATTTATTTA
- TTATTTATTTATTTA
- TTATTTATTTATTTATTTATTTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355364
feature_type: variation
id: rs1177091887
seq_region_name: 17
source: dbSNP
start: 73355346
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355348
feature_type: variation
id: rs1455778453
seq_region_name: 17
source: dbSNP
start: 73355348
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355351
feature_type: variation
id: rs1026618052
seq_region_name: 17
source: dbSNP
start: 73355351
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355354
feature_type: variation
id: rs2062583128
seq_region_name: 17
source: dbSNP
start: 73355354
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355360
feature_type: variation
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73355372
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062583450
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source: dbSNP
start: 73355395
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062583472
seq_region_name: 17
source: dbSNP
start: 73355397
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs369732966
seq_region_name: 17
source: dbSNP
start: 73355402
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs187274230
seq_region_name: 17
source: dbSNP
start: 73355403
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs906061914
seq_region_name: 17
source: dbSNP
start: 73355403
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs551961788
seq_region_name: 17
source: dbSNP
start: 73355409
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1036211669
seq_region_name: 17
source: dbSNP
start: 73355410
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1303547264
seq_region_name: 17
source: dbSNP
start: 73355418
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1166213322
seq_region_name: 17
source: dbSNP
start: 73355419
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1353512785
seq_region_name: 17
source: dbSNP
start: 73355424
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355425
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355426
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062583814
seq_region_name: 17
source: dbSNP
start: 73355428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062583905
seq_region_name: 17
source: dbSNP
start: 73355432
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355433
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1440708967
seq_region_name: 17
source: dbSNP
start: 73355433
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145408404
seq_region_name: 17
source: dbSNP
start: 73355434
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1186011530
seq_region_name: 17
source: dbSNP
start: 73355439
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs978874506
seq_region_name: 17
source: dbSNP
start: 73355440
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355441
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs73343850
seq_region_name: 17
source: dbSNP
start: 73355449
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062584161
seq_region_name: 17
source: dbSNP
start: 73355454
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355455
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs144989884
seq_region_name: 17
source: dbSNP
start: 73355460
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1052009505
seq_region_name: 17
source: dbSNP
start: 73355461
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs375694422
seq_region_name: 17
source: dbSNP
start: 73355462
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1215563621
seq_region_name: 17
source: dbSNP
start: 73355463
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs940845801
seq_region_name: 17
source: dbSNP
start: 73355465
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062584348
seq_region_name: 17
source: dbSNP
start: 73355466
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062584377
seq_region_name: 17
source: dbSNP
start: 73355471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs921868755
seq_region_name: 17
source: dbSNP
start: 73355474
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062584429
seq_region_name: 17
source: dbSNP
start: 73355475
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062584450
seq_region_name: 17
source: dbSNP
start: 73355476
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355481
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355484
feature_type: variation
id: rs1036492154
seq_region_name: 17
source: dbSNP
start: 73355484
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355485
feature_type: variation
id: rs2145408532
seq_region_name: 17
source: dbSNP
start: 73355485
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355486
feature_type: variation
id: rs896878184
seq_region_name: 17
source: dbSNP
start: 73355486
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1242489824
seq_region_name: 17
source: dbSNP
start: 73355487
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1339862728
seq_region_name: 17
source: dbSNP
start: 73355489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs995211163
seq_region_name: 17
source: dbSNP
start: 73355490
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062584599
seq_region_name: 17
source: dbSNP
start: 73355491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs953356258
seq_region_name: 17
source: dbSNP
start: 73355496
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1416700509
seq_region_name: 17
source: dbSNP
start: 73355497
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73355501
feature_type: variation
id: rs1338632624
seq_region_name: 17
source: dbSNP
start: 73355501
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355503
feature_type: variation
id: rs2062584705
seq_region_name: 17
source: dbSNP
start: 73355503
strand: 1
-
alleles:
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- TTTTATTTTTTATTTTT
- TTTTATTTTTTATTTTTTATTTTTTATTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355527
feature_type: variation
id: rs987309428
seq_region_name: 17
source: dbSNP
start: 73355504
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355514
feature_type: variation
id: rs2062584771
seq_region_name: 17
source: dbSNP
start: 73355509
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062584785
seq_region_name: 17
source: dbSNP
start: 73355516
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293536059
seq_region_name: 17
source: dbSNP
start: 73355516
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355528
feature_type: variation
id: rs2062584827
seq_region_name: 17
source: dbSNP
start: 73355517
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355521
feature_type: variation
id: rs796532031
seq_region_name: 17
source: dbSNP
start: 73355521
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355521
feature_type: variation
id: rs1026732353
seq_region_name: 17
source: dbSNP
start: 73355521
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355522
feature_type: variation
id: rs911697955
seq_region_name: 17
source: dbSNP
start: 73355522
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355523
feature_type: variation
id: rs1599478413
seq_region_name: 17
source: dbSNP
start: 73355523
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355529
feature_type: variation
id: rs2062584953
seq_region_name: 17
source: dbSNP
start: 73355529
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355530
feature_type: variation
id: rs4482356
seq_region_name: 17
source: dbSNP
start: 73355530
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355535
feature_type: variation
id: rs2062585029
seq_region_name: 17
source: dbSNP
start: 73355535
strand: 1
-
alleles:
- GGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355540
feature_type: variation
id: rs1036031760
seq_region_name: 17
source: dbSNP
start: 73355537
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355539
feature_type: variation
id: rs2062585115
seq_region_name: 17
source: dbSNP
start: 73355539
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355540
feature_type: variation
id: rs576826705
seq_region_name: 17
source: dbSNP
start: 73355540
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355541
feature_type: variation
id: rs2062585173
seq_region_name: 17
source: dbSNP
start: 73355541
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355544
feature_type: variation
id: rs2145408696
seq_region_name: 17
source: dbSNP
start: 73355544
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355547
feature_type: variation
id: rs2062585198
seq_region_name: 17
source: dbSNP
start: 73355547
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355548
feature_type: variation
id: rs2062585224
seq_region_name: 17
source: dbSNP
start: 73355548
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355549
feature_type: variation
id: rs2062585256
seq_region_name: 17
source: dbSNP
start: 73355549
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355551
feature_type: variation
id: rs1260540126
seq_region_name: 17
source: dbSNP
start: 73355551
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355555
feature_type: variation
id: rs544090916
seq_region_name: 17
source: dbSNP
start: 73355555
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355556
feature_type: variation
id: rs192104076
seq_region_name: 17
source: dbSNP
start: 73355556
strand: 1
-
alleles:
- GAG
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355558
feature_type: variation
id: rs386799012
seq_region_name: 17
source: dbSNP
start: 73355556
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73355705
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73355719
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73355720
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73355725
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73355729
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73355730
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73355734
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73355744
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73355755
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73355755
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73355756
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73355757
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355759
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355762
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355768
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355772
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355774
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355783
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355787
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73355790
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355941
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355945
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1599478774
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355966
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355967
strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs1353738845
seq_region_name: 17
source: dbSNP
start: 73355973
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355976
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs927025659
seq_region_name: 17
source: dbSNP
start: 73355989
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs773625006
seq_region_name: 17
source: dbSNP
start: 73355990
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73355992
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355994
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355996
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73355998
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs557909112
seq_region_name: 17
source: dbSNP
start: 73355999
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1029014231
seq_region_name: 17
source: dbSNP
start: 73356000
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062589504
seq_region_name: 17
source: dbSNP
start: 73356001
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1056921094
seq_region_name: 17
source: dbSNP
start: 73356003
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599478813
seq_region_name: 17
source: dbSNP
start: 73356022
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs889076431
seq_region_name: 17
source: dbSNP
start: 73356023
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062589605
seq_region_name: 17
source: dbSNP
start: 73356028
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs537789316
seq_region_name: 17
source: dbSNP
start: 73356030
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356031
feature_type: variation
id: rs373065295
seq_region_name: 17
source: dbSNP
start: 73356031
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356032
feature_type: variation
id: rs1211540064
seq_region_name: 17
source: dbSNP
start: 73356032
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062589693
seq_region_name: 17
source: dbSNP
start: 73356035
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1334887863
seq_region_name: 17
source: dbSNP
start: 73356040
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356043
feature_type: variation
id: rs1009933902
seq_region_name: 17
source: dbSNP
start: 73356043
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356044
feature_type: variation
id: rs2062589764
seq_region_name: 17
source: dbSNP
start: 73356044
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356051
feature_type: variation
id: rs2062589792
seq_region_name: 17
source: dbSNP
start: 73356051
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356052
feature_type: variation
id: rs961895045
seq_region_name: 17
source: dbSNP
start: 73356052
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73356194
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73356208
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73356218
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73356218
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73356219
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356223
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356228
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs7207820
seq_region_name: 17
source: dbSNP
start: 73356229
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356230
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356234
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356235
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356237
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356240
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356245
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356249
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145410199
seq_region_name: 17
source: dbSNP
start: 73356253
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356263
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062591429
seq_region_name: 17
source: dbSNP
start: 73356264
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1276287567
seq_region_name: 17
source: dbSNP
start: 73356265
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356266
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356269
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs545727521
seq_region_name: 17
source: dbSNP
start: 73356270
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145410265
seq_region_name: 17
source: dbSNP
start: 73356273
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1041408041
seq_region_name: 17
source: dbSNP
start: 73356284
strand: 1
-
alleles:
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- CCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062591535
seq_region_name: 17
source: dbSNP
start: 73356284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs564205539
seq_region_name: 17
source: dbSNP
start: 73356285
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73356286
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id: rs528359708
seq_region_name: 17
source: dbSNP
start: 73356286
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs78918305
seq_region_name: 17
source: dbSNP
start: 73356288
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1478642970
seq_region_name: 17
source: dbSNP
start: 73356289
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1000106780
seq_region_name: 17
source: dbSNP
start: 73356290
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73356292
feature_type: variation
id: rs1050406977
seq_region_name: 17
source: dbSNP
start: 73356292
strand: 1
-
alleles:
- G
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73356481
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73356482
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73356492
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356495
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356497
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73356497
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356498
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356510
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356512
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356513
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73356518
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356519
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145410823
seq_region_name: 17
source: dbSNP
start: 73356524
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356525
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356527
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356528
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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end: 73356534
feature_type: variation
id: rs1337626779
seq_region_name: 17
source: dbSNP
start: 73356534
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73356705
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73356706
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356710
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356714
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73356716
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73356719
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356720
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73356722
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356723
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356726
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356734
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356742
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356747
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356748
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356749
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356751
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356753
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356757
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356760
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356761
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73356771
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356773
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73356776
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id: rs1210559959
seq_region_name: 17
source: dbSNP
start: 73356776
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73356980
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73356982
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73356985
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73357001
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357003
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357011
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs896512294
seq_region_name: 17
source: dbSNP
start: 73357012
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357016
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1258321215
seq_region_name: 17
source: dbSNP
start: 73357019
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357022
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357026
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145411782
seq_region_name: 17
source: dbSNP
start: 73357027
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1270660059
seq_region_name: 17
source: dbSNP
start: 73357035
strand: 1
-
alleles:
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- AGGG
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357035
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357036
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1212541195
seq_region_name: 17
source: dbSNP
start: 73357038
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs957871523
seq_region_name: 17
source: dbSNP
start: 73357041
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1021242194
seq_region_name: 17
source: dbSNP
start: 73357043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs966856492
seq_region_name: 17
source: dbSNP
start: 73357046
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1212487601
seq_region_name: 17
source: dbSNP
start: 73357050
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73357173
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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start: 73357179
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73357207
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73357208
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357210
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357213
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357215
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357217
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357218
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357222
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357224
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs902787961
seq_region_name: 17
source: dbSNP
start: 73357228
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357231
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357233
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357236
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1467967997
seq_region_name: 17
source: dbSNP
start: 73357237
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1032501861
seq_region_name: 17
source: dbSNP
start: 73357242
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357244
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062599644
seq_region_name: 17
source: dbSNP
start: 73357245
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357248
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357249
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357254
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357256
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357257
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357260
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357263
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062599840
seq_region_name: 17
source: dbSNP
start: 73357265
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062599855
seq_region_name: 17
source: dbSNP
start: 73357266
strand: 1
-
alleles:
- "-"
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357271
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357271
feature_type: variation
id: rs1017798379
seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73357463
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73357489
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73357489
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73357501
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357509
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357513
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357517
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73357531
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73357532
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73357534
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357545
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357549
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357550
feature_type: variation
id: rs1453784172
seq_region_name: 17
source: dbSNP
start: 73357550
strand: 1
-
alleles:
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assembly_name: GRCh38
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-
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-
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357682
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357686
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357688
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357691
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145413201
seq_region_name: 17
source: dbSNP
start: 73357699
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357703
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357704
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357708
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357709
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357713
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357719
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357721
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357722
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357723
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599480343
seq_region_name: 17
source: dbSNP
start: 73357724
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357727
feature_type: variation
id: rs2145413259
seq_region_name: 17
source: dbSNP
start: 73357727
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1398941832
seq_region_name: 17
source: dbSNP
start: 73357730
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357734
feature_type: variation
id: rs2145413273
seq_region_name: 17
source: dbSNP
start: 73357734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357737
feature_type: variation
id: rs2062603488
seq_region_name: 17
source: dbSNP
start: 73357737
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357740
feature_type: variation
id: rs977966489
seq_region_name: 17
source: dbSNP
start: 73357737
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357738
feature_type: variation
id: rs901383713
seq_region_name: 17
source: dbSNP
start: 73357738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1473664723
seq_region_name: 17
source: dbSNP
start: 73357741
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357745
feature_type: variation
id: rs936513729
seq_region_name: 17
source: dbSNP
start: 73357745
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357746
feature_type: variation
id: rs2062603661
seq_region_name: 17
source: dbSNP
start: 73357746
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357750
feature_type: variation
id: rs2062603706
seq_region_name: 17
source: dbSNP
start: 73357750
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357755
feature_type: variation
id: rs2062603758
seq_region_name: 17
source: dbSNP
start: 73357755
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599480359
seq_region_name: 17
source: dbSNP
start: 73357757
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs535715636
seq_region_name: 17
source: dbSNP
start: 73357758
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357760
feature_type: variation
id: rs2145413338
seq_region_name: 17
source: dbSNP
start: 73357760
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357761
feature_type: variation
id: rs2062603878
seq_region_name: 17
source: dbSNP
start: 73357761
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357767
feature_type: variation
id: rs942414491
seq_region_name: 17
source: dbSNP
start: 73357767
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357770
feature_type: variation
id: rs1214256064
seq_region_name: 17
source: dbSNP
start: 73357770
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357771
feature_type: variation
id: rs2062603931
seq_region_name: 17
source: dbSNP
start: 73357771
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357772
feature_type: variation
id: rs1026044042
seq_region_name: 17
source: dbSNP
start: 73357772
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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feature_type: variation
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357858
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062604946
seq_region_name: 17
source: dbSNP
start: 73357859
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs769984739
seq_region_name: 17
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start: 73357861
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357870
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357873
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs752069681
seq_region_name: 17
source: dbSNP
start: 73357876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs554281055
seq_region_name: 17
source: dbSNP
start: 73357879
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357882
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357883
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357884
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357886
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1484254257
seq_region_name: 17
source: dbSNP
start: 73357887
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062605357
seq_region_name: 17
source: dbSNP
start: 73357889
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73357892
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062605410
seq_region_name: 17
source: dbSNP
start: 73357894
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs752242400
seq_region_name: 17
source: dbSNP
start: 73357899
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs755649486
seq_region_name: 17
source: dbSNP
start: 73357900
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs777342083
seq_region_name: 17
source: dbSNP
start: 73357910
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357911
feature_type: variation
id: rs748955167
seq_region_name: 17
source: dbSNP
start: 73357911
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568364200
seq_region_name: 17
source: dbSNP
start: 73357912
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357913
feature_type: variation
id: rs756997726
seq_region_name: 17
source: dbSNP
start: 73357913
strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357918
feature_type: variation
id: rs1568364207
seq_region_name: 17
source: dbSNP
start: 73357913
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357914
feature_type: variation
id: rs1165664551
seq_region_name: 17
source: dbSNP
start: 73357914
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357915
feature_type: variation
id: rs778711874
seq_region_name: 17
source: dbSNP
start: 73357915
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357916
feature_type: variation
id: rs1169181401
seq_region_name: 17
source: dbSNP
start: 73357916
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357918
feature_type: variation
id: rs930175058
seq_region_name: 17
source: dbSNP
start: 73357918
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357920
feature_type: variation
id: rs1391728493
seq_region_name: 17
source: dbSNP
start: 73357920
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357921
feature_type: variation
id: rs1047442132
seq_region_name: 17
source: dbSNP
start: 73357921
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357926
feature_type: variation
id: rs1427552610
seq_region_name: 17
source: dbSNP
start: 73357926
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357929
feature_type: variation
id: rs2062605780
seq_region_name: 17
source: dbSNP
start: 73357929
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357933
feature_type: variation
id: rs1568364224
seq_region_name: 17
source: dbSNP
start: 73357933
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357933
feature_type: variation
id: rs2145413780
seq_region_name: 17
source: dbSNP
start: 73357933
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357935
feature_type: variation
id: rs745712009
seq_region_name: 17
source: dbSNP
start: 73357935
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357936
feature_type: variation
id: rs2062605840
seq_region_name: 17
source: dbSNP
start: 73357936
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357940
feature_type: variation
id: rs774247323
seq_region_name: 17
source: dbSNP
start: 73357940
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357941
feature_type: variation
id: rs775356038
seq_region_name: 17
source: dbSNP
start: 73357941
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357943
feature_type: variation
id: rs1250521987
seq_region_name: 17
source: dbSNP
start: 73357943
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357945
feature_type: variation
id: rs1300506835
seq_region_name: 17
source: dbSNP
start: 73357945
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357946
feature_type: variation
id: rs1377811776
seq_region_name: 17
source: dbSNP
start: 73357946
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357950
feature_type: variation
id: rs1245831155
seq_region_name: 17
source: dbSNP
start: 73357950
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357953
feature_type: variation
id: rs2062605994
seq_region_name: 17
source: dbSNP
start: 73357953
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357955
feature_type: variation
id: rs1190133451
seq_region_name: 17
source: dbSNP
start: 73357955
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357958
feature_type: variation
id: rs1599480631
seq_region_name: 17
source: dbSNP
start: 73357958
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357959
feature_type: variation
id: rs748190436
seq_region_name: 17
source: dbSNP
start: 73357959
strand: 1
-
alleles:
- TGTA
- TGTATGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357964
feature_type: variation
id: rs2062606053
seq_region_name: 17
source: dbSNP
start: 73357961
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357962
feature_type: variation
id: rs2062606075
seq_region_name: 17
source: dbSNP
start: 73357962
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357963
feature_type: variation
id: rs1248122460
seq_region_name: 17
source: dbSNP
start: 73357963
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357964
feature_type: variation
id: rs1568364245
seq_region_name: 17
source: dbSNP
start: 73357964
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357965
feature_type: variation
id: rs761757663
seq_region_name: 17
source: dbSNP
start: 73357965
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357966
feature_type: variation
id: rs1226645360
seq_region_name: 17
source: dbSNP
start: 73357966
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357969
feature_type: variation
id: rs773516499
seq_region_name: 17
source: dbSNP
start: 73357969
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357971
feature_type: variation
id: rs1312935297
seq_region_name: 17
source: dbSNP
start: 73357971
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357973
feature_type: variation
id: rs989339915
seq_region_name: 17
source: dbSNP
start: 73357972
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357975
feature_type: variation
id: rs73343872
seq_region_name: 17
source: dbSNP
start: 73357975
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357976
feature_type: variation
id: rs774838976
seq_region_name: 17
source: dbSNP
start: 73357976
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357977
feature_type: variation
id: rs2062606285
seq_region_name: 17
source: dbSNP
start: 73357977
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357983
feature_type: variation
id: rs2062606311
seq_region_name: 17
source: dbSNP
start: 73357983
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357987
feature_type: variation
id: rs750219142
seq_region_name: 17
source: dbSNP
start: 73357987
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357988
feature_type: variation
id: rs753151747
seq_region_name: 17
source: dbSNP
start: 73357988
strand: 1
-
alleles:
- ACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357995
feature_type: variation
id: rs1452609157
seq_region_name: 17
source: dbSNP
start: 73357993
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73357998
feature_type: variation
id: rs755594009
seq_region_name: 17
source: dbSNP
start: 73357998
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358004
feature_type: variation
id: rs1219910521
seq_region_name: 17
source: dbSNP
start: 73358004
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358006
feature_type: variation
id: rs763617474
seq_region_name: 17
source: dbSNP
start: 73358006
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358009
feature_type: variation
id: rs1447650135
seq_region_name: 17
source: dbSNP
start: 73358006
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358007
feature_type: variation
id: rs1425623422
seq_region_name: 17
source: dbSNP
start: 73358007
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358009
feature_type: variation
id: rs138950824
seq_region_name: 17
source: dbSNP
start: 73358009
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358011
feature_type: variation
id: rs778593502
seq_region_name: 17
source: dbSNP
start: 73358011
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358012
feature_type: variation
id: rs1404965102
seq_region_name: 17
source: dbSNP
start: 73358012
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358017
feature_type: variation
id: rs750226379
seq_region_name: 17
source: dbSNP
start: 73358017
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358019
feature_type: variation
id: rs1380627139
seq_region_name: 17
source: dbSNP
start: 73358019
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358021
feature_type: variation
id: rs1310240954
seq_region_name: 17
source: dbSNP
start: 73358021
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358022
feature_type: variation
id: rs2062606708
seq_region_name: 17
source: dbSNP
start: 73358022
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358023
feature_type: variation
id: rs1322052925
seq_region_name: 17
source: dbSNP
start: 73358023
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358024
feature_type: variation
id: rs1433337205
seq_region_name: 17
source: dbSNP
start: 73358024
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358025
feature_type: variation
id: rs779980931
seq_region_name: 17
source: dbSNP
start: 73358025
strand: 1
-
alleles:
- GA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358027
feature_type: variation
id: rs2062606775
seq_region_name: 17
source: dbSNP
start: 73358026
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358028
feature_type: variation
id: rs746938622
seq_region_name: 17
source: dbSNP
start: 73358028
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358029
feature_type: variation
id: rs7216718
seq_region_name: 17
source: dbSNP
start: 73358029
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358032
feature_type: variation
id: rs2062606896
seq_region_name: 17
source: dbSNP
start: 73358032
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358033
feature_type: variation
id: rs372008625
seq_region_name: 17
source: dbSNP
start: 73358033
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358034
feature_type: variation
id: rs1568364296
seq_region_name: 17
source: dbSNP
start: 73358034
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358036
feature_type: variation
id: rs376912577
seq_region_name: 17
source: dbSNP
start: 73358036
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358037
feature_type: variation
id: rs369489196
seq_region_name: 17
source: dbSNP
start: 73358037
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358038
feature_type: variation
id: rs774783981
seq_region_name: 17
source: dbSNP
start: 73358038
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358041
feature_type: variation
id: rs373185379
seq_region_name: 17
source: dbSNP
start: 73358041
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358043
feature_type: variation
id: rs866312038
seq_region_name: 17
source: dbSNP
start: 73358043
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358044
feature_type: variation
id: rs2062607079
seq_region_name: 17
source: dbSNP
start: 73358044
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358046
feature_type: variation
id: rs772338770
seq_region_name: 17
source: dbSNP
start: 73358046
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358048
feature_type: variation
id: rs776017866
seq_region_name: 17
source: dbSNP
start: 73358048
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358049
feature_type: variation
id: rs761118648
seq_region_name: 17
source: dbSNP
start: 73358049
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358050
feature_type: variation
id: rs1247026159
seq_region_name: 17
source: dbSNP
start: 73358050
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358056
feature_type: variation
id: rs1478899225
seq_region_name: 17
source: dbSNP
start: 73358056
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358059
feature_type: variation
id: rs764625780
seq_region_name: 17
source: dbSNP
start: 73358059
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358060
feature_type: variation
id: rs2062607252
seq_region_name: 17
source: dbSNP
start: 73358060
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358061
feature_type: variation
id: rs753333014
seq_region_name: 17
source: dbSNP
start: 73358061
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358066
feature_type: variation
id: rs377432222
seq_region_name: 17
source: dbSNP
start: 73358066
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358067
feature_type: variation
id: rs369906390
seq_region_name: 17
source: dbSNP
start: 73358067
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358068
feature_type: variation
id: rs2062607349
seq_region_name: 17
source: dbSNP
start: 73358068
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358069
feature_type: variation
id: rs374087560
seq_region_name: 17
source: dbSNP
start: 73358069
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358070
feature_type: variation
id: rs764801679
seq_region_name: 17
source: dbSNP
start: 73358070
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73358072
feature_type: variation
id: rs200499035
seq_region_name: 17
source: dbSNP
start: 73358072
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73358073
feature_type: variation
id: rs370247077
seq_region_name: 17
source: dbSNP
start: 73358073
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73358074
feature_type: variation
id: rs112549542
seq_region_name: 17
source: dbSNP
start: 73358074
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73358075
feature_type: variation
id: rs376714866
seq_region_name: 17
source: dbSNP
start: 73358075
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73358077
feature_type: variation
id: rs1599480860
seq_region_name: 17
source: dbSNP
start: 73358077
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358085
feature_type: variation
id: rs1439008909
seq_region_name: 17
source: dbSNP
start: 73358085
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358086
feature_type: variation
id: rs1281844987
seq_region_name: 17
source: dbSNP
start: 73358086
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358089
feature_type: variation
id: rs1345102610
seq_region_name: 17
source: dbSNP
start: 73358089
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358090
feature_type: variation
id: rs2062607590
seq_region_name: 17
source: dbSNP
start: 73358090
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73358091
feature_type: variation
id: rs1229256041
seq_region_name: 17
source: dbSNP
start: 73358091
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358092
feature_type: variation
id: rs1413352267
seq_region_name: 17
source: dbSNP
start: 73358092
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358095
feature_type: variation
id: rs754940512
seq_region_name: 17
source: dbSNP
start: 73358095
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73358097
feature_type: variation
id: rs781340211
seq_region_name: 17
source: dbSNP
start: 73358097
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358098
feature_type: variation
id: rs1303916928
seq_region_name: 17
source: dbSNP
start: 73358098
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358100
feature_type: variation
id: rs1468085082
seq_region_name: 17
source: dbSNP
start: 73358100
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73358101
feature_type: variation
id: rs895267442
seq_region_name: 17
source: dbSNP
start: 73358101
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358105
feature_type: variation
id: rs1290467976
seq_region_name: 17
source: dbSNP
start: 73358105
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358106
feature_type: variation
id: rs371296779
seq_region_name: 17
source: dbSNP
start: 73358106
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358108
feature_type: variation
id: rs1161794946
seq_region_name: 17
source: dbSNP
start: 73358108
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358113
feature_type: variation
id: rs1219094490
seq_region_name: 17
source: dbSNP
start: 73358113
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73358115
feature_type: variation
id: rs1568364360
seq_region_name: 17
source: dbSNP
start: 73358113
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358114
feature_type: variation
id: rs771142129
seq_region_name: 17
source: dbSNP
start: 73358114
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358115
feature_type: variation
id: rs1472677698
seq_region_name: 17
source: dbSNP
start: 73358115
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358116
feature_type: variation
id: rs1184033126
seq_region_name: 17
source: dbSNP
start: 73358116
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358117
feature_type: variation
id: rs1413247614
seq_region_name: 17
source: dbSNP
start: 73358117
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358120
feature_type: variation
id: rs1183941451
seq_region_name: 17
source: dbSNP
start: 73358120
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358124
feature_type: variation
id: rs764879893
seq_region_name: 17
source: dbSNP
start: 73358124
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358125
feature_type: variation
id: rs376014699
seq_region_name: 17
source: dbSNP
start: 73358125
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358126
feature_type: variation
id: rs370149165
seq_region_name: 17
source: dbSNP
start: 73358126
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358128
feature_type: variation
id: rs1258977518
seq_region_name: 17
source: dbSNP
start: 73358128
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358133
feature_type: variation
id: rs1163372107
seq_region_name: 17
source: dbSNP
start: 73358133
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358134
feature_type: variation
id: rs144308459
seq_region_name: 17
source: dbSNP
start: 73358134
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358135
feature_type: variation
id: rs1330037710
seq_region_name: 17
source: dbSNP
start: 73358135
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73358140
feature_type: variation
id: rs2062608293
seq_region_name: 17
source: dbSNP
start: 73358140
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358143
feature_type: variation
id: rs199537367
seq_region_name: 17
source: dbSNP
start: 73358143
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358146
feature_type: variation
id: rs1301613588
seq_region_name: 17
source: dbSNP
start: 73358146
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358148
feature_type: variation
id: rs761159020
seq_region_name: 17
source: dbSNP
start: 73358148
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358151
feature_type: variation
id: rs769147060
seq_region_name: 17
source: dbSNP
start: 73358151
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358152
feature_type: variation
id: rs777125372
seq_region_name: 17
source: dbSNP
start: 73358152
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358154
feature_type: variation
id: rs2062608492
seq_region_name: 17
source: dbSNP
start: 73358154
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358156
feature_type: variation
id: rs761254539
seq_region_name: 17
source: dbSNP
start: 73358156
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358158
feature_type: variation
id: rs764745965
seq_region_name: 17
source: dbSNP
start: 73358158
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358160
feature_type: variation
id: rs750050320
seq_region_name: 17
source: dbSNP
start: 73358160
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358163
feature_type: variation
id: rs1358311174
seq_region_name: 17
source: dbSNP
start: 73358163
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73358168
feature_type: variation
id: rs762478016
seq_region_name: 17
source: dbSNP
start: 73358168
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73358169
feature_type: variation
id: rs766101018
seq_region_name: 17
source: dbSNP
start: 73358169
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358172
feature_type: variation
id: rs751302864
seq_region_name: 17
source: dbSNP
start: 73358172
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358173
feature_type: variation
id: rs2062608755
seq_region_name: 17
source: dbSNP
start: 73358173
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358174
feature_type: variation
id: rs1599481050
seq_region_name: 17
source: dbSNP
start: 73358174
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358175
feature_type: variation
id: rs2145414486
seq_region_name: 17
source: dbSNP
start: 73358175
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358176
feature_type: variation
id: rs754413721
seq_region_name: 17
source: dbSNP
start: 73358176
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358182
feature_type: variation
id: rs922871587
seq_region_name: 17
source: dbSNP
start: 73358182
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358184
feature_type: variation
id: rs146597384
seq_region_name: 17
source: dbSNP
start: 73358184
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358185
feature_type: variation
id: rs999511365
seq_region_name: 17
source: dbSNP
start: 73358185
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358186
feature_type: variation
id: rs1456127006
seq_region_name: 17
source: dbSNP
start: 73358186
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358191
feature_type: variation
id: rs367842935
seq_region_name: 17
source: dbSNP
start: 73358191
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358192
feature_type: variation
id: rs1187620267
seq_region_name: 17
source: dbSNP
start: 73358192
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358193
feature_type: variation
id: rs2062609097
seq_region_name: 17
source: dbSNP
start: 73358193
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358199
feature_type: variation
id: rs2062609128
seq_region_name: 17
source: dbSNP
start: 73358199
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73358200
feature_type: variation
id: rs1369708601
seq_region_name: 17
source: dbSNP
start: 73358200
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73358202
feature_type: variation
id: rs757365277
seq_region_name: 17
source: dbSNP
start: 73358202
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73358203
feature_type: variation
id: rs1165232295
seq_region_name: 17
source: dbSNP
start: 73358203
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73358205
feature_type: variation
id: rs1162255913
seq_region_name: 17
source: dbSNP
start: 73358205
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73358208
feature_type: variation
id: rs1384947429
seq_region_name: 17
source: dbSNP
start: 73358208
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73358212
feature_type: variation
id: rs1425432876
seq_region_name: 17
source: dbSNP
start: 73358212
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358214
feature_type: variation
id: rs1568364459
seq_region_name: 17
source: dbSNP
start: 73358214
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358215
feature_type: variation
id: rs746000714
seq_region_name: 17
source: dbSNP
start: 73358215
strand: 1
-
alleles:
- CACACA
- CACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358220
feature_type: variation
id: rs754531365
seq_region_name: 17
source: dbSNP
start: 73358215
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358216
feature_type: variation
id: rs2062609407
seq_region_name: 17
source: dbSNP
start: 73358216
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358217
feature_type: variation
id: rs143271650
seq_region_name: 17
source: dbSNP
start: 73358217
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358218
feature_type: variation
id: rs1394588167
seq_region_name: 17
source: dbSNP
start: 73358218
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358219
feature_type: variation
id: rs1391053448
seq_region_name: 17
source: dbSNP
start: 73358219
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73358221
feature_type: variation
id: rs1334842570
seq_region_name: 17
source: dbSNP
start: 73358221
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358222
feature_type: variation
id: rs1342377779
seq_region_name: 17
source: dbSNP
start: 73358222
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358225
feature_type: variation
id: rs199795619
seq_region_name: 17
source: dbSNP
start: 73358225
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358226
feature_type: variation
id: rs747307311
seq_region_name: 17
source: dbSNP
start: 73358226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358228
feature_type: variation
id: rs1280587669
seq_region_name: 17
source: dbSNP
start: 73358228
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358230
feature_type: variation
id: rs769020230
seq_region_name: 17
source: dbSNP
start: 73358230
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358231
feature_type: variation
id: rs1230326133
seq_region_name: 17
source: dbSNP
start: 73358231
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358237
feature_type: variation
id: rs1249457028
seq_region_name: 17
source: dbSNP
start: 73358237
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358241
feature_type: variation
id: rs989763354
seq_region_name: 17
source: dbSNP
start: 73358241
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358243
feature_type: variation
id: rs1355922509
seq_region_name: 17
source: dbSNP
start: 73358241
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358242
feature_type: variation
id: rs1200684044
seq_region_name: 17
source: dbSNP
start: 73358242
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358244
feature_type: variation
id: rs1018114439
seq_region_name: 17
source: dbSNP
start: 73358244
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358248
feature_type: variation
id: rs777072226
seq_region_name: 17
source: dbSNP
start: 73358248
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358252
feature_type: variation
id: rs2062609848
seq_region_name: 17
source: dbSNP
start: 73358252
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358254
feature_type: variation
id: rs2062609871
seq_region_name: 17
source: dbSNP
start: 73358254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358256
feature_type: variation
id: rs1306230868
seq_region_name: 17
source: dbSNP
start: 73358256
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358258
feature_type: variation
id: rs1297472944
seq_region_name: 17
source: dbSNP
start: 73358258
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358259
feature_type: variation
id: rs941769593
seq_region_name: 17
source: dbSNP
start: 73358259
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358260
feature_type: variation
id: rs2145414756
seq_region_name: 17
source: dbSNP
start: 73358260
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358261
feature_type: variation
id: rs201914146
seq_region_name: 17
source: dbSNP
start: 73358261
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358262
feature_type: variation
id: rs147535994
seq_region_name: 17
source: dbSNP
start: 73358262
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358264
feature_type: variation
id: rs1011925742
seq_region_name: 17
source: dbSNP
start: 73358264
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358265
feature_type: variation
id: rs2062610036
seq_region_name: 17
source: dbSNP
start: 73358265
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358266
feature_type: variation
id: rs1599481202
seq_region_name: 17
source: dbSNP
start: 73358266
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358267
feature_type: variation
id: rs2062610085
seq_region_name: 17
source: dbSNP
start: 73358267
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358268
feature_type: variation
id: rs2062610112
seq_region_name: 17
source: dbSNP
start: 73358268
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358270
feature_type: variation
id: rs2062610139
seq_region_name: 17
source: dbSNP
start: 73358270
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358275
feature_type: variation
id: rs1389591710
seq_region_name: 17
source: dbSNP
start: 73358275
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358276
feature_type: variation
id: rs139499309
seq_region_name: 17
source: dbSNP
start: 73358276
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358280
feature_type: variation
id: rs1459218333
seq_region_name: 17
source: dbSNP
start: 73358280
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358285
feature_type: variation
id: rs1388138188
seq_region_name: 17
source: dbSNP
start: 73358285
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358286
feature_type: variation
id: rs1167874665
seq_region_name: 17
source: dbSNP
start: 73358286
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358289
feature_type: variation
id: rs2062610226
seq_region_name: 17
source: dbSNP
start: 73358289
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358290
feature_type: variation
id: rs929674571
seq_region_name: 17
source: dbSNP
start: 73358290
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358291
feature_type: variation
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73358416
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358421
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358422
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358426
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358428
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358440
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358447
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358460
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1275001965
seq_region_name: 17
source: dbSNP
start: 73358462
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358465
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358467
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358468
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358475
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145415209
seq_region_name: 17
source: dbSNP
start: 73358476
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs916349746
seq_region_name: 17
source: dbSNP
start: 73358477
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599481396
seq_region_name: 17
source: dbSNP
start: 73358481
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062612022
seq_region_name: 17
source: dbSNP
start: 73358487
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062612069
seq_region_name: 17
source: dbSNP
start: 73358490
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062612128
seq_region_name: 17
source: dbSNP
start: 73358492
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs77971918
seq_region_name: 17
source: dbSNP
start: 73358498
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062612216
seq_region_name: 17
source: dbSNP
start: 73358502
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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end: 73358503
feature_type: variation
id: rs1337067882
seq_region_name: 17
source: dbSNP
start: 73358503
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358504
feature_type: variation
id: rs145012700
seq_region_name: 17
source: dbSNP
start: 73358504
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358506
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358511
feature_type: variation
id: rs935233177
seq_region_name: 17
source: dbSNP
start: 73358511
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062612436
seq_region_name: 17
source: dbSNP
start: 73358513
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1455795374
seq_region_name: 17
source: dbSNP
start: 73358515
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062612492
seq_region_name: 17
source: dbSNP
start: 73358516
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358521
feature_type: variation
id: rs2062612515
seq_region_name: 17
source: dbSNP
start: 73358521
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358522
feature_type: variation
id: rs2062612536
seq_region_name: 17
source: dbSNP
start: 73358522
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358525
feature_type: variation
id: rs1052375290
seq_region_name: 17
source: dbSNP
start: 73358525
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358531
feature_type: variation
id: rs1183210524
seq_region_name: 17
source: dbSNP
start: 73358531
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358534
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id: rs2062612596
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358697
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358699
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358701
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73358706
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358707
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358708
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358711
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358712
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358715
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358716
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1437531026
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73358819
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73358820
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358821
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73358822
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73358823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358824
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358825
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358830
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358832
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358833
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358834
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73358835
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358837
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73358839
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358842
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358844
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358850
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73358854
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358855
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358856
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73358860
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73358861
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358863
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs981844249
seq_region_name: 17
source: dbSNP
start: 73358865
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs553936852
seq_region_name: 17
source: dbSNP
start: 73358866
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs72853930
seq_region_name: 17
source: dbSNP
start: 73358867
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358868
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358869
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599481852
seq_region_name: 17
source: dbSNP
start: 73358876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062616375
seq_region_name: 17
source: dbSNP
start: 73358879
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358884
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73358884
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358886
feature_type: variation
id: rs1266448419
seq_region_name: 17
source: dbSNP
start: 73358886
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358887
feature_type: variation
id: rs1255298495
seq_region_name: 17
source: dbSNP
start: 73358887
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358888
feature_type: variation
id: rs534168261
seq_region_name: 17
source: dbSNP
start: 73358888
strand: 1
-
alleles:
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs987828580
seq_region_name: 17
source: dbSNP
start: 73358893
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358899
feature_type: variation
id: rs915110176
seq_region_name: 17
source: dbSNP
start: 73358899
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358901
feature_type: variation
id: rs2145416217
seq_region_name: 17
source: dbSNP
start: 73358901
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73358903
feature_type: variation
id: rs946648823
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source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359049
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359058
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73359059
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359060
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359062
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73359063
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359074
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359078
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359082
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359086
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359087
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359088
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359089
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359090
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359095
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359100
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2055039488
seq_region_name: 17
source: dbSNP
start: 73359101
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs956455252
seq_region_name: 17
source: dbSNP
start: 73359111
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs988323314
seq_region_name: 17
source: dbSNP
start: 73359112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1374922885
seq_region_name: 17
source: dbSNP
start: 73359113
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1174963121
seq_region_name: 17
source: dbSNP
start: 73359115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1845727067
seq_region_name: 17
source: dbSNP
start: 73359118
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062618967
seq_region_name: 17
source: dbSNP
start: 73359119
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359122
feature_type: variation
id: rs2062619004
seq_region_name: 17
source: dbSNP
start: 73359122
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359123
feature_type: variation
id: rs2062619032
seq_region_name: 17
source: dbSNP
start: 73359123
strand: 1
-
alleles:
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- GTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062619064
seq_region_name: 17
source: dbSNP
start: 73359123
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359124
feature_type: variation
id: rs2062619079
seq_region_name: 17
source: dbSNP
start: 73359124
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359126
feature_type: variation
id: rs2062619104
seq_region_name: 17
source: dbSNP
start: 73359126
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359128
feature_type: variation
id: rs2062619136
seq_region_name: 17
source: dbSNP
start: 73359128
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359129
feature_type: variation
id: rs988371502
seq_region_name: 17
source: dbSNP
start: 73359129
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359137
feature_type: variation
id: rs2062619215
seq_region_name: 17
source: dbSNP
start: 73359137
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062619253
seq_region_name: 17
source: dbSNP
start: 73359142
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359147
feature_type: variation
id: rs756359323
seq_region_name: 17
source: dbSNP
start: 73359147
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359149
feature_type: variation
id: rs914892567
seq_region_name: 17
source: dbSNP
start: 73359149
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599482112
seq_region_name: 17
source: dbSNP
start: 73359151
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359153
feature_type: variation
id: rs1022895028
seq_region_name: 17
source: dbSNP
start: 73359153
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062619451
seq_region_name: 17
source: dbSNP
start: 73359154
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359155
feature_type: variation
id: rs2062619473
seq_region_name: 17
source: dbSNP
start: 73359155
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359157
feature_type: variation
id: rs2062619493
seq_region_name: 17
source: dbSNP
start: 73359157
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359158
feature_type: variation
id: rs1274520917
seq_region_name: 17
source: dbSNP
start: 73359158
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359159
feature_type: variation
id: rs968237690
seq_region_name: 17
source: dbSNP
start: 73359159
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359160
feature_type: variation
id: rs2062619569
seq_region_name: 17
source: dbSNP
start: 73359160
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359163
feature_type: variation
id: rs1170022630
seq_region_name: 17
source: dbSNP
start: 73359163
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359165
feature_type: variation
id: rs2062619610
seq_region_name: 17
source: dbSNP
start: 73359165
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062619632
seq_region_name: 17
source: dbSNP
start: 73359166
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359167
feature_type: variation
id: rs2145416825
seq_region_name: 17
source: dbSNP
start: 73359167
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1339469683
seq_region_name: 17
source: dbSNP
start: 73359170
strand: 1
-
alleles:
- GGG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359173
feature_type: variation
id: rs548569028
seq_region_name: 17
source: dbSNP
start: 73359171
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359173
feature_type: variation
id: rs1230536679
seq_region_name: 17
source: dbSNP
start: 73359173
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359174
feature_type: variation
id: rs968155566
seq_region_name: 17
source: dbSNP
start: 73359174
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359180
feature_type: variation
id: rs1283637603
seq_region_name: 17
source: dbSNP
start: 73359180
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359183
feature_type: variation
id: rs2062619786
seq_region_name: 17
source: dbSNP
start: 73359183
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359184
feature_type: variation
id: rs975346128
seq_region_name: 17
source: dbSNP
start: 73359184
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359192
feature_type: variation
id: rs2062619820
seq_region_name: 17
source: dbSNP
start: 73359192
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359193
feature_type: variation
id: rs142174864
seq_region_name: 17
source: dbSNP
start: 73359193
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359194
feature_type: variation
id: rs2062619886
seq_region_name: 17
source: dbSNP
start: 73359194
strand: 1
-
alleles:
- GGGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359199
feature_type: variation
id: rs2062619910
seq_region_name: 17
source: dbSNP
start: 73359194
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359197
feature_type: variation
id: rs574074803
seq_region_name: 17
source: dbSNP
start: 73359197
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359198
feature_type: variation
id: rs1385280927
seq_region_name: 17
source: dbSNP
start: 73359198
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359199
feature_type: variation
id: rs1398650067
seq_region_name: 17
source: dbSNP
start: 73359199
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359200
feature_type: variation
id: rs1756161839
seq_region_name: 17
source: dbSNP
start: 73359200
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359201
feature_type: variation
id: rs376806251
seq_region_name: 17
source: dbSNP
start: 73359201
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359209
feature_type: variation
id: rs1201917387
seq_region_name: 17
source: dbSNP
start: 73359209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359210
feature_type: variation
id: rs908414312
seq_region_name: 17
source: dbSNP
start: 73359210
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359217
feature_type: variation
id: rs1471805950
seq_region_name: 17
source: dbSNP
start: 73359217
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359219
feature_type: variation
id: rs1675537923
seq_region_name: 17
source: dbSNP
start: 73359219
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359222
feature_type: variation
id: rs2145416929
seq_region_name: 17
source: dbSNP
start: 73359222
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359227
feature_type: variation
id: rs2062620118
seq_region_name: 17
source: dbSNP
start: 73359227
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359234
feature_type: variation
id: rs1251630369
seq_region_name: 17
source: dbSNP
start: 73359234
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359235
feature_type: variation
id: rs1444722932
seq_region_name: 17
source: dbSNP
start: 73359235
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359238
feature_type: variation
id: rs2062620193
seq_region_name: 17
source: dbSNP
start: 73359238
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359240
feature_type: variation
id: rs1229248890
seq_region_name: 17
source: dbSNP
start: 73359240
strand: 1
-
alleles:
- GGCCCTGGAGGGCCAGCAGGCCCT
- GGCCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359266
feature_type: variation
id: rs1440072525
seq_region_name: 17
source: dbSNP
start: 73359243
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359244
feature_type: variation
id: rs1251983941
seq_region_name: 17
source: dbSNP
start: 73359244
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359245
feature_type: variation
id: rs1198258647
seq_region_name: 17
source: dbSNP
start: 73359245
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359247
feature_type: variation
id: rs2062620293
seq_region_name: 17
source: dbSNP
start: 73359247
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359248
feature_type: variation
id: rs2145416984
seq_region_name: 17
source: dbSNP
start: 73359248
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359249
feature_type: variation
id: rs2062620313
seq_region_name: 17
source: dbSNP
start: 73359249
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359253
feature_type: variation
id: rs2062620338
seq_region_name: 17
source: dbSNP
start: 73359253
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359254
feature_type: variation
id: rs2062620362
seq_region_name: 17
source: dbSNP
start: 73359254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359256
feature_type: variation
id: rs2062620384
seq_region_name: 17
source: dbSNP
start: 73359256
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359257
feature_type: variation
id: rs2062620409
seq_region_name: 17
source: dbSNP
start: 73359257
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359258
feature_type: variation
id: rs2062620429
seq_region_name: 17
source: dbSNP
start: 73359258
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359259
feature_type: variation
id: rs1322264280
seq_region_name: 17
source: dbSNP
start: 73359259
strand: 1
-
alleles:
- CCC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359265
feature_type: variation
id: rs2062620477
seq_region_name: 17
source: dbSNP
start: 73359263
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359267
feature_type: variation
id: rs940101856
seq_region_name: 17
source: dbSNP
start: 73359267
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359268
feature_type: variation
id: rs2145417038
seq_region_name: 17
source: dbSNP
start: 73359268
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359270
feature_type: variation
id: rs1225031713
seq_region_name: 17
source: dbSNP
start: 73359270
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359274
feature_type: variation
id: rs1326813949
seq_region_name: 17
source: dbSNP
start: 73359274
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359277
feature_type: variation
id: rs527865371
seq_region_name: 17
source: dbSNP
start: 73359277
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359278
feature_type: variation
id: rs939939548
seq_region_name: 17
source: dbSNP
start: 73359278
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359284
feature_type: variation
id: rs549525324
seq_region_name: 17
source: dbSNP
start: 73359284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359286
feature_type: variation
id: rs898489100
seq_region_name: 17
source: dbSNP
start: 73359286
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359289
feature_type: variation
id: rs1599482225
seq_region_name: 17
source: dbSNP
start: 73359289
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359289
feature_type: variation
id: rs2145417073
seq_region_name: 17
source: dbSNP
start: 73359289
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359292
feature_type: variation
id: rs567782313
seq_region_name: 17
source: dbSNP
start: 73359292
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359293
feature_type: variation
id: rs2062620816
seq_region_name: 17
source: dbSNP
start: 73359293
strand: 1
-
alleles:
- GGCCACTATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359302
feature_type: variation
id: rs2145417090
seq_region_name: 17
source: dbSNP
start: 73359293
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359294
feature_type: variation
id: rs2062620843
seq_region_name: 17
source: dbSNP
start: 73359294
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359295
feature_type: variation
id: rs2062620868
seq_region_name: 17
source: dbSNP
start: 73359295
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359298
feature_type: variation
id: rs1332232628
seq_region_name: 17
source: dbSNP
start: 73359298
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359299
feature_type: variation
id: rs2062620929
seq_region_name: 17
source: dbSNP
start: 73359299
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359304
feature_type: variation
id: rs2145417114
seq_region_name: 17
source: dbSNP
start: 73359304
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1254299449
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source: dbSNP
start: 73359314
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1178845273
seq_region_name: 17
source: dbSNP
start: 73359316
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599482255
seq_region_name: 17
source: dbSNP
start: 73359318
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359320
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359324
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145417165
seq_region_name: 17
source: dbSNP
start: 73359325
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359332
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1044612308
seq_region_name: 17
source: dbSNP
start: 73359334
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1367201107
seq_region_name: 17
source: dbSNP
start: 73359334
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs151183210
seq_region_name: 17
source: dbSNP
start: 73359335
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs571503607
seq_region_name: 17
source: dbSNP
start: 73359336
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145417212
seq_region_name: 17
source: dbSNP
start: 73359339
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062621544
seq_region_name: 17
source: dbSNP
start: 73359343
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062621583
seq_region_name: 17
source: dbSNP
start: 73359351
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1261928329
seq_region_name: 17
source: dbSNP
start: 73359352
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs66884550
seq_region_name: 17
source: dbSNP
start: 73359353
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs140293146
seq_region_name: 17
source: dbSNP
start: 73359354
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565903691
seq_region_name: 17
source: dbSNP
start: 73359356
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1463282707
seq_region_name: 17
source: dbSNP
start: 73359361
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145417249
seq_region_name: 17
source: dbSNP
start: 73359363
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359370
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1283237037
seq_region_name: 17
source: dbSNP
start: 73359371
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1044196379
seq_region_name: 17
source: dbSNP
start: 73359373
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1031829351
seq_region_name: 17
source: dbSNP
start: 73359374
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs891990695
seq_region_name: 17
source: dbSNP
start: 73359377
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs776522852
seq_region_name: 17
source: dbSNP
start: 73359380
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062622083
seq_region_name: 17
source: dbSNP
start: 73359383
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145417278
seq_region_name: 17
source: dbSNP
start: 73359384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062622123
seq_region_name: 17
source: dbSNP
start: 73359385
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1009314022
seq_region_name: 17
source: dbSNP
start: 73359386
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1022496193
seq_region_name: 17
source: dbSNP
start: 73359388
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359390
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359392
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359395
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062622325
seq_region_name: 17
source: dbSNP
start: 73359401
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359402
feature_type: variation
id: rs2062622365
seq_region_name: 17
source: dbSNP
start: 73359402
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359413
feature_type: variation
id: rs2062622391
seq_region_name: 17
source: dbSNP
start: 73359413
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359416
feature_type: variation
id: rs554318714
seq_region_name: 17
source: dbSNP
start: 73359416
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359422
feature_type: variation
id: rs575739177
seq_region_name: 17
source: dbSNP
start: 73359422
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359423
feature_type: variation
id: rs759044155
seq_region_name: 17
source: dbSNP
start: 73359423
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359429
feature_type: variation
id: rs764996163
seq_region_name: 17
source: dbSNP
start: 73359429
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359431
feature_type: variation
id: rs1362913055
seq_region_name: 17
source: dbSNP
start: 73359431
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs955279759
seq_region_name: 17
source: dbSNP
start: 73359432
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359435
feature_type: variation
id: rs2062622562
seq_region_name: 17
source: dbSNP
start: 73359432
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359434
feature_type: variation
id: rs1163186245
seq_region_name: 17
source: dbSNP
start: 73359434
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359440
feature_type: variation
id: rs2062622591
seq_region_name: 17
source: dbSNP
start: 73359440
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359442
feature_type: variation
id: rs1445775271
seq_region_name: 17
source: dbSNP
start: 73359442
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359443
feature_type: variation
id: rs2062622654
seq_region_name: 17
source: dbSNP
start: 73359443
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359444
feature_type: variation
id: rs986704752
seq_region_name: 17
source: dbSNP
start: 73359444
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359450
feature_type: variation
id: rs2145417394
seq_region_name: 17
source: dbSNP
start: 73359450
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359451
feature_type: variation
id: rs2145417403
seq_region_name: 17
source: dbSNP
start: 73359451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359452
feature_type: variation
id: rs1184925219
seq_region_name: 17
source: dbSNP
start: 73359452
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359453
feature_type: variation
id: rs968212415
seq_region_name: 17
source: dbSNP
start: 73359453
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359456
feature_type: variation
id: rs536698230
seq_region_name: 17
source: dbSNP
start: 73359456
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359457
feature_type: variation
id: rs908381815
seq_region_name: 17
source: dbSNP
start: 73359457
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359458
feature_type: variation
id: rs2062622850
seq_region_name: 17
source: dbSNP
start: 73359458
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359460
feature_type: variation
id: rs2062622881
seq_region_name: 17
source: dbSNP
start: 73359460
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359464
feature_type: variation
id: rs2145417437
seq_region_name: 17
source: dbSNP
start: 73359464
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359465
feature_type: variation
id: rs2145417443
seq_region_name: 17
source: dbSNP
start: 73359465
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359466
feature_type: variation
id: rs1599482404
seq_region_name: 17
source: dbSNP
start: 73359466
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359470
feature_type: variation
id: rs2145417454
seq_region_name: 17
source: dbSNP
start: 73359470
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359474
feature_type: variation
id: rs1599482411
seq_region_name: 17
source: dbSNP
start: 73359474
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359478
feature_type: variation
id: rs1599482418
seq_region_name: 17
source: dbSNP
start: 73359478
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359480
feature_type: variation
id: rs2062623023
seq_region_name: 17
source: dbSNP
start: 73359480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359481
feature_type: variation
id: rs2062623049
seq_region_name: 17
source: dbSNP
start: 73359481
strand: 1
-
alleles:
- CTCAGGACCCTGTACTCA
- CTCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359500
feature_type: variation
id: rs1241127684
seq_region_name: 17
source: dbSNP
start: 73359483
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359485
feature_type: variation
id: rs1216126623
seq_region_name: 17
source: dbSNP
start: 73359485
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359490
feature_type: variation
id: rs1384191525
seq_region_name: 17
source: dbSNP
start: 73359490
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359491
feature_type: variation
id: rs939884029
seq_region_name: 17
source: dbSNP
start: 73359491
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359492
feature_type: variation
id: rs558567635
seq_region_name: 17
source: dbSNP
start: 73359492
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359493
feature_type: variation
id: rs2062623175
seq_region_name: 17
source: dbSNP
start: 73359493
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359499
feature_type: variation
id: rs2062623203
seq_region_name: 17
source: dbSNP
start: 73359499
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359505
feature_type: variation
id: rs2062623221
seq_region_name: 17
source: dbSNP
start: 73359505
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359509
feature_type: variation
id: rs768179836
seq_region_name: 17
source: dbSNP
start: 73359509
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359512
feature_type: variation
id: rs920008559
seq_region_name: 17
source: dbSNP
start: 73359512
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359513
feature_type: variation
id: rs948725757
seq_region_name: 17
source: dbSNP
start: 73359513
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359516
feature_type: variation
id: rs1226232103
seq_region_name: 17
source: dbSNP
start: 73359516
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359519
feature_type: variation
id: rs1044429347
seq_region_name: 17
source: dbSNP
start: 73359519
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359520
feature_type: variation
id: rs907230424
seq_region_name: 17
source: dbSNP
start: 73359520
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73359699
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359701
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359708
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73359711
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73359720
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73359722
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359724
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359727
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359729
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359731
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359732
feature_type: variation
id: rs1599482600
seq_region_name: 17
source: dbSNP
start: 73359732
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359870
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359882
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359888
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359889
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359894
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359895
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73359896
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359901
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359903
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73359906
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359907
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359911
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359912
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73359913
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73359921
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs890758012
seq_region_name: 17
source: dbSNP
start: 73359922
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1384427420
seq_region_name: 17
source: dbSNP
start: 73359926
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73359928
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs900150637
seq_region_name: 17
source: dbSNP
start: 73359929
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062627273
seq_region_name: 17
source: dbSNP
start: 73359933
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359937
feature_type: variation
id: rs547700292
seq_region_name: 17
source: dbSNP
start: 73359937
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1362318219
seq_region_name: 17
source: dbSNP
start: 73359938
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1290432851
seq_region_name: 17
source: dbSNP
start: 73359939
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062627370
seq_region_name: 17
source: dbSNP
start: 73359941
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1422620533
seq_region_name: 17
source: dbSNP
start: 73359943
strand: 1
-
alleles:
- TTCTTTCTTTCT
- TTCTTTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359955
feature_type: variation
id: rs1281145185
seq_region_name: 17
source: dbSNP
start: 73359944
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1007852748
seq_region_name: 17
source: dbSNP
start: 73359946
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359947
feature_type: variation
id: rs1426611811
seq_region_name: 17
source: dbSNP
start: 73359947
strand: 1
-
alleles:
- TTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359949
feature_type: variation
id: rs997085969
seq_region_name: 17
source: dbSNP
start: 73359947
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359955
feature_type: variation
id: rs1371474855
seq_region_name: 17
source: dbSNP
start: 73359955
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73359956
feature_type: variation
id: rs1192658754
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360182
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360199
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360205
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360210
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360214
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360216
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360217
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360219
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360224
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360225
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360227
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360228
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360229
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360230
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73360231
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seq_region_name: 17
source: dbSNP
start: 73360231
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73360234
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360234
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360265
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360267
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1821953945
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360291
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360293
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360294
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs944249231
seq_region_name: 17
source: dbSNP
start: 73360298
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1037219748
seq_region_name: 17
source: dbSNP
start: 73360302
strand: 1
-
alleles:
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- AGAAAGTGACTGGCCAGAAAGAGAAAGTGACTGGCCAGAAAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062629752
seq_region_name: 17
source: dbSNP
start: 73360303
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360306
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360307
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs543298058
seq_region_name: 17
source: dbSNP
start: 73360308
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360309
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs995826148
seq_region_name: 17
source: dbSNP
start: 73360310
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062629871
seq_region_name: 17
source: dbSNP
start: 73360311
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1407069218
seq_region_name: 17
source: dbSNP
start: 73360316
strand: 1
-
alleles:
- AGAAAGAAA
- AGAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs751024636
seq_region_name: 17
source: dbSNP
start: 73360318
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1338996530
seq_region_name: 17
source: dbSNP
start: 73360324
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360325
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs969842632
seq_region_name: 17
source: dbSNP
start: 73360327
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360330
strand: 1
-
alleles:
- AAGC
- AAGCAAGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs995631670
seq_region_name: 17
source: dbSNP
start: 73360332
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360335
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs149154670
seq_region_name: 17
source: dbSNP
start: 73360336
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360340
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360342
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360349
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1186887180
seq_region_name: 17
source: dbSNP
start: 73360352
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1181249907
seq_region_name: 17
source: dbSNP
start: 73360356
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360359
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360362
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062630327
seq_region_name: 17
source: dbSNP
start: 73360364
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062630348
seq_region_name: 17
source: dbSNP
start: 73360365
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062630377
seq_region_name: 17
source: dbSNP
start: 73360366
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145419184
seq_region_name: 17
source: dbSNP
start: 73360367
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360372
feature_type: variation
id: rs1463982489
seq_region_name: 17
source: dbSNP
start: 73360372
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360373
feature_type: variation
id: rs1599483129
seq_region_name: 17
source: dbSNP
start: 73360373
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1169813968
seq_region_name: 17
source: dbSNP
start: 73360374
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062630436
seq_region_name: 17
source: dbSNP
start: 73360380
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062630460
seq_region_name: 17
source: dbSNP
start: 73360381
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360383
feature_type: variation
id: rs2062630488
seq_region_name: 17
source: dbSNP
start: 73360383
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360386
feature_type: variation
id: rs756525626
seq_region_name: 17
source: dbSNP
start: 73360386
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360390
feature_type: variation
id: rs988919697
seq_region_name: 17
source: dbSNP
start: 73360390
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360393
feature_type: variation
id: rs2062630550
seq_region_name: 17
source: dbSNP
start: 73360393
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360394
feature_type: variation
id: rs532612806
seq_region_name: 17
source: dbSNP
start: 73360394
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs143345258
seq_region_name: 17
source: dbSNP
start: 73360397
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360402
feature_type: variation
id: rs1245307382
seq_region_name: 17
source: dbSNP
start: 73360402
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360404
feature_type: variation
id: rs989108743
seq_region_name: 17
source: dbSNP
start: 73360404
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360406
feature_type: variation
id: rs968784246
seq_region_name: 17
source: dbSNP
start: 73360406
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360413
feature_type: variation
id: rs1406537311
seq_region_name: 17
source: dbSNP
start: 73360413
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360414
feature_type: variation
id: rs780249893
seq_region_name: 17
source: dbSNP
start: 73360414
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360415
feature_type: variation
id: rs1319416678
seq_region_name: 17
source: dbSNP
start: 73360415
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360418
feature_type: variation
id: rs4969111
seq_region_name: 17
source: dbSNP
start: 73360418
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360421
feature_type: variation
id: rs1364218310
seq_region_name: 17
source: dbSNP
start: 73360421
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360423
feature_type: variation
id: rs12452120
seq_region_name: 17
source: dbSNP
start: 73360423
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360424
feature_type: variation
id: rs2062630869
seq_region_name: 17
source: dbSNP
start: 73360424
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360431
feature_type: variation
id: rs978521628
seq_region_name: 17
source: dbSNP
start: 73360431
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360432
feature_type: variation
id: rs1385390513
seq_region_name: 17
source: dbSNP
start: 73360432
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360433
feature_type: variation
id: rs2062630935
seq_region_name: 17
source: dbSNP
start: 73360433
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360434
feature_type: variation
id: rs932128948
seq_region_name: 17
source: dbSNP
start: 73360434
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360435
feature_type: variation
id: rs1599483201
seq_region_name: 17
source: dbSNP
start: 73360435
strand: 1
-
alleles:
- GAGGAGGAG
- GAGGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360449
feature_type: variation
id: rs2062631010
seq_region_name: 17
source: dbSNP
start: 73360441
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360443
feature_type: variation
id: rs1474232202
seq_region_name: 17
source: dbSNP
start: 73360443
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360444
feature_type: variation
id: rs1279200602
seq_region_name: 17
source: dbSNP
start: 73360444
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360445
feature_type: variation
id: rs1051893783
seq_region_name: 17
source: dbSNP
start: 73360445
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360447
feature_type: variation
id: rs867213694
seq_region_name: 17
source: dbSNP
start: 73360447
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360449
feature_type: variation
id: rs2062631125
seq_region_name: 17
source: dbSNP
start: 73360449
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360451
feature_type: variation
id: rs1599483217
seq_region_name: 17
source: dbSNP
start: 73360450
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360453
feature_type: variation
id: rs2145419363
seq_region_name: 17
source: dbSNP
start: 73360453
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360464
feature_type: variation
id: rs943771563
seq_region_name: 17
source: dbSNP
start: 73360464
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73360669
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360675
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360680
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73360682
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360683
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73360687
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360688
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360697
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360699
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360703
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360708
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360709
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360710
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360712
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360715
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360721
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360723
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360729
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs905953093
seq_region_name: 17
source: dbSNP
start: 73360732
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73360734
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360734
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360742
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360742
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360743
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360743
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360744
feature_type: variation
id: rs1001483194
seq_region_name: 17
source: dbSNP
start: 73360744
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73360895
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360912
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360919
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73360919
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360921
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360921
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360922
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360923
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360924
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360927
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360927
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73360932
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360934
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360935
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1367840406
seq_region_name: 17
source: dbSNP
start: 73360936
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062634516
seq_region_name: 17
source: dbSNP
start: 73360937
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360938
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73360938
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1265957951
seq_region_name: 17
source: dbSNP
start: 73360939
strand: 1
-
alleles:
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- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1262851160
seq_region_name: 17
source: dbSNP
start: 73360939
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs80331697
seq_region_name: 17
source: dbSNP
start: 73360940
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062634704
seq_region_name: 17
source: dbSNP
start: 73360947
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360954
feature_type: variation
id: rs1599483568
seq_region_name: 17
source: dbSNP
start: 73360954
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360959
feature_type: variation
id: rs2062634744
seq_region_name: 17
source: dbSNP
start: 73360959
strand: 1
-
alleles:
- AACAACAACAACA
- AACAACAACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73360971
feature_type: variation
id: rs973047075
seq_region_name: 17
source: dbSNP
start: 73360959
strand: 1
-
alleles:
- A
- G
- T
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73361081
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73361101
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73361103
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73361104
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361105
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361106
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73361111
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73361116
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73361123
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361128
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73361128
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73361130
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361135
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73361138
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seq_region_name: 17
source: dbSNP
start: 73361138
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361139
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1235331715
seq_region_name: 17
source: dbSNP
start: 73361141
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73361327
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73361336
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73361339
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73361342
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73361343
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361348
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361349
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361350
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361351
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73361501
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73361510
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73361514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73361516
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73361517
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73361521
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361525
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1027744694
seq_region_name: 17
source: dbSNP
start: 73361529
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73361530
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062640027
seq_region_name: 17
source: dbSNP
start: 73361530
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73361532
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73361535
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73361536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1008854172
seq_region_name: 17
source: dbSNP
start: 73361537
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1175256888
seq_region_name: 17
source: dbSNP
start: 73361541
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361541
feature_type: variation
id: rs2062640185
seq_region_name: 17
source: dbSNP
start: 73361541
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361543
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73361543
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361545
feature_type: variation
id: rs1427317623
seq_region_name: 17
source: dbSNP
start: 73361545
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361547
feature_type: variation
id: rs1176812470
seq_region_name: 17
source: dbSNP
start: 73361547
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361548
feature_type: variation
id: rs1439188613
seq_region_name: 17
source: dbSNP
start: 73361548
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361549
feature_type: variation
id: rs1238957488
seq_region_name: 17
source: dbSNP
start: 73361549
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361552
feature_type: variation
id: rs2062640320
seq_region_name: 17
source: dbSNP
start: 73361552
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361555
feature_type: variation
id: rs2062640340
seq_region_name: 17
source: dbSNP
start: 73361555
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361558
feature_type: variation
id: rs1019129989
seq_region_name: 17
source: dbSNP
start: 73361558
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361572
feature_type: variation
id: rs1460254619
seq_region_name: 17
source: dbSNP
start: 73361572
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361574
feature_type: variation
id: rs1237321981
seq_region_name: 17
source: dbSNP
start: 73361574
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361575
feature_type: variation
id: rs993408947
seq_region_name: 17
source: dbSNP
start: 73361575
strand: 1
-
alleles:
- CTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361583
feature_type: variation
id: rs35151121
seq_region_name: 17
source: dbSNP
start: 73361580
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361581
feature_type: variation
id: rs1599484126
seq_region_name: 17
source: dbSNP
start: 73361581
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361587
feature_type: variation
id: rs962331061
seq_region_name: 17
source: dbSNP
start: 73361587
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361588
feature_type: variation
id: rs977520754
seq_region_name: 17
source: dbSNP
start: 73361588
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361590
feature_type: variation
id: rs4969112
seq_region_name: 17
source: dbSNP
start: 73361590
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361597
feature_type: variation
id: rs994181880
seq_region_name: 17
source: dbSNP
start: 73361597
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361599
feature_type: variation
id: rs1263483972
seq_region_name: 17
source: dbSNP
start: 73361599
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361601
feature_type: variation
id: rs1352343578
seq_region_name: 17
source: dbSNP
start: 73361601
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361603
feature_type: variation
id: rs2145421776
seq_region_name: 17
source: dbSNP
start: 73361603
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361604
feature_type: variation
id: rs1027822070
seq_region_name: 17
source: dbSNP
start: 73361604
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361610
feature_type: variation
id: rs2062640755
seq_region_name: 17
source: dbSNP
start: 73361610
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361614
feature_type: variation
id: rs556969712
seq_region_name: 17
source: dbSNP
start: 73361614
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361615
feature_type: variation
id: rs2062640810
seq_region_name: 17
source: dbSNP
start: 73361615
strand: 1
-
alleles:
- GGGGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361619
feature_type: variation
id: rs2145421800
seq_region_name: 17
source: dbSNP
start: 73361615
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361617
feature_type: variation
id: rs983839734
seq_region_name: 17
source: dbSNP
start: 73361617
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361618
feature_type: variation
id: rs1568365695
seq_region_name: 17
source: dbSNP
start: 73361618
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361622
feature_type: variation
id: rs2145421821
seq_region_name: 17
source: dbSNP
start: 73361622
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361623
feature_type: variation
id: rs2062640889
seq_region_name: 17
source: dbSNP
start: 73361623
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361624
feature_type: variation
id: rs1376673438
seq_region_name: 17
source: dbSNP
start: 73361624
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361632
feature_type: variation
id: rs570381571
seq_region_name: 17
source: dbSNP
start: 73361632
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361636
feature_type: variation
id: rs1599484169
seq_region_name: 17
source: dbSNP
start: 73361636
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361637
feature_type: variation
id: rs770370842
seq_region_name: 17
source: dbSNP
start: 73361637
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361638
feature_type: variation
id: rs1568365700
seq_region_name: 17
source: dbSNP
start: 73361638
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361638
feature_type: variation
id: rs2062641002
seq_region_name: 17
source: dbSNP
start: 73361638
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361639
feature_type: variation
id: rs772570631
seq_region_name: 17
source: dbSNP
start: 73361639
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361640
feature_type: variation
id: rs374813371
seq_region_name: 17
source: dbSNP
start: 73361640
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361643
feature_type: variation
id: rs1599484180
seq_region_name: 17
source: dbSNP
start: 73361643
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361645
feature_type: variation
id: rs765946730
seq_region_name: 17
source: dbSNP
start: 73361645
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361646
feature_type: variation
id: rs368295307
seq_region_name: 17
source: dbSNP
start: 73361646
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361648
feature_type: variation
id: rs759349908
seq_region_name: 17
source: dbSNP
start: 73361648
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361649
feature_type: variation
id: rs767445874
seq_region_name: 17
source: dbSNP
start: 73361649
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361651
feature_type: variation
id: rs537711118
seq_region_name: 17
source: dbSNP
start: 73361651
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361652
feature_type: variation
id: rs2062641233
seq_region_name: 17
source: dbSNP
start: 73361652
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361653
feature_type: variation
id: rs756089097
seq_region_name: 17
source: dbSNP
start: 73361653
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361656
feature_type: variation
id: rs2145421926
seq_region_name: 17
source: dbSNP
start: 73361656
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361658
feature_type: variation
id: rs1404677558
seq_region_name: 17
source: dbSNP
start: 73361658
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361659
feature_type: variation
id: rs1251233105
seq_region_name: 17
source: dbSNP
start: 73361659
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361660
feature_type: variation
id: rs764142165
seq_region_name: 17
source: dbSNP
start: 73361660
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361665
feature_type: variation
id: rs750464044
seq_region_name: 17
source: dbSNP
start: 73361665
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361667
feature_type: variation
id: rs371982267
seq_region_name: 17
source: dbSNP
start: 73361667
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361668
feature_type: variation
id: rs758509920
seq_region_name: 17
source: dbSNP
start: 73361668
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361670
feature_type: variation
id: rs375308250
seq_region_name: 17
source: dbSNP
start: 73361670
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361671
feature_type: variation
id: rs2279732
seq_region_name: 17
source: dbSNP
start: 73361671
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361674
feature_type: variation
id: rs1216609127
seq_region_name: 17
source: dbSNP
start: 73361674
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73361677
feature_type: variation
id: rs781502646
seq_region_name: 17
source: dbSNP
start: 73361677
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73361678
feature_type: variation
id: rs1555751885
seq_region_name: 17
source: dbSNP
start: 73361678
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73361679
feature_type: variation
id: rs748556887
seq_region_name: 17
source: dbSNP
start: 73361679
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73361680
feature_type: variation
id: rs780617916
seq_region_name: 17
source: dbSNP
start: 73361679
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73361682
feature_type: variation
id: rs2062641628
seq_region_name: 17
source: dbSNP
start: 73361682
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: missense_variant
end: 73361689
feature_type: variation
id: rs138527765
seq_region_name: 17
source: dbSNP
start: 73361689
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361690
feature_type: variation
id: rs541199916
seq_region_name: 17
source: dbSNP
start: 73361690
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361691
feature_type: variation
id: rs748684023
seq_region_name: 17
source: dbSNP
start: 73361691
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361693
feature_type: variation
id: rs770491431
seq_region_name: 17
source: dbSNP
start: 73361693
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361697
feature_type: variation
id: rs373585421
seq_region_name: 17
source: dbSNP
start: 73361697
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361698
feature_type: variation
id: rs374728907
seq_region_name: 17
source: dbSNP
start: 73361698
strand: 1
-
alleles:
- GTG
- GTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73361700
feature_type: variation
id: rs2145422102
seq_region_name: 17
source: dbSNP
start: 73361698
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361699
feature_type: variation
id: rs775403568
seq_region_name: 17
source: dbSNP
start: 73361699
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361702
feature_type: variation
id: rs1189873973
seq_region_name: 17
source: dbSNP
start: 73361702
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361703
feature_type: variation
id: rs2062641936
seq_region_name: 17
source: dbSNP
start: 73361703
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361705
feature_type: variation
id: rs369267841
seq_region_name: 17
source: dbSNP
start: 73361705
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361706
feature_type: variation
id: rs372814522
seq_region_name: 17
source: dbSNP
start: 73361706
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361707
feature_type: variation
id: rs753827757
seq_region_name: 17
source: dbSNP
start: 73361707
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361708
feature_type: variation
id: rs762890901
seq_region_name: 17
source: dbSNP
start: 73361708
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361710
feature_type: variation
id: rs2062642084
seq_region_name: 17
source: dbSNP
start: 73361710
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361714
feature_type: variation
id: rs766510308
seq_region_name: 17
source: dbSNP
start: 73361714
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361715
feature_type: variation
id: rs377212719
seq_region_name: 17
source: dbSNP
start: 73361715
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361721
feature_type: variation
id: rs8067373
seq_region_name: 17
source: dbSNP
start: 73361721
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361722
feature_type: variation
id: rs574562964
seq_region_name: 17
source: dbSNP
start: 73361722
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361726
feature_type: variation
id: rs1384228683
seq_region_name: 17
source: dbSNP
start: 73361726
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73361727
feature_type: variation
id: rs145884780
seq_region_name: 17
source: dbSNP
start: 73361727
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361728
feature_type: variation
id: rs753052485
seq_region_name: 17
source: dbSNP
start: 73361728
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361729
feature_type: variation
id: rs756510262
seq_region_name: 17
source: dbSNP
start: 73361729
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361731
feature_type: variation
id: rs2062642348
seq_region_name: 17
source: dbSNP
start: 73361731
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361732
feature_type: variation
id: rs1165759274
seq_region_name: 17
source: dbSNP
start: 73361732
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361733
feature_type: variation
id: rs2062642397
seq_region_name: 17
source: dbSNP
start: 73361733
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361737
feature_type: variation
id: rs959233679
seq_region_name: 17
source: dbSNP
start: 73361737
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361742
feature_type: variation
id: rs1288383502
seq_region_name: 17
source: dbSNP
start: 73361742
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361750
feature_type: variation
id: rs1422006523
seq_region_name: 17
source: dbSNP
start: 73361750
strand: 1
-
alleles:
- GCGGAACCTGTAGGTCACCCCCTCCGC
- GC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73361777
feature_type: variation
id: rs752202112
seq_region_name: 17
source: dbSNP
start: 73361751
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361752
feature_type: variation
id: rs993067545
seq_region_name: 17
source: dbSNP
start: 73361752
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361753
feature_type: variation
id: rs1266015702
seq_region_name: 17
source: dbSNP
start: 73361753
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361757
feature_type: variation
id: rs778088866
seq_region_name: 17
source: dbSNP
start: 73361757
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361758
feature_type: variation
id: rs1487227023
seq_region_name: 17
source: dbSNP
start: 73361758
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361760
feature_type: variation
id: rs1259452545
seq_region_name: 17
source: dbSNP
start: 73361760
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361765
feature_type: variation
id: rs1485863401
seq_region_name: 17
source: dbSNP
start: 73361765
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361767
feature_type: variation
id: rs1599484421
seq_region_name: 17
source: dbSNP
start: 73361767
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73361772
feature_type: variation
id: rs2145422372
seq_region_name: 17
source: dbSNP
start: 73361768
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361769
feature_type: variation
id: rs749826231
seq_region_name: 17
source: dbSNP
start: 73361769
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361770
feature_type: variation
id: rs1271515930
seq_region_name: 17
source: dbSNP
start: 73361770
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361771
feature_type: variation
id: rs1479543006
seq_region_name: 17
source: dbSNP
start: 73361771
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361774
feature_type: variation
id: rs2062642826
seq_region_name: 17
source: dbSNP
start: 73361774
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361775
feature_type: variation
id: rs201069071
seq_region_name: 17
source: dbSNP
start: 73361775
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361776
feature_type: variation
id: rs541836618
seq_region_name: 17
source: dbSNP
start: 73361776
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361777
feature_type: variation
id: rs1323269995
seq_region_name: 17
source: dbSNP
start: 73361777
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361778
feature_type: variation
id: rs2062642957
seq_region_name: 17
source: dbSNP
start: 73361778
strand: 1
-
alleles:
- TCCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73361785
feature_type: variation
id: rs1276122035
seq_region_name: 17
source: dbSNP
start: 73361782
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361783
feature_type: variation
id: rs1420936560
seq_region_name: 17
source: dbSNP
start: 73361783
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361786
feature_type: variation
id: rs80316089
seq_region_name: 17
source: dbSNP
start: 73361786
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361788
feature_type: variation
id: rs2062643098
seq_region_name: 17
source: dbSNP
start: 73361788
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361789
feature_type: variation
id: rs745421895
seq_region_name: 17
source: dbSNP
start: 73361789
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361790
feature_type: variation
id: rs148821721
seq_region_name: 17
source: dbSNP
start: 73361790
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361793
feature_type: variation
id: rs1458359840
seq_region_name: 17
source: dbSNP
start: 73361793
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361798
feature_type: variation
id: rs1341004612
seq_region_name: 17
source: dbSNP
start: 73361798
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361802
feature_type: variation
id: rs977948082
seq_region_name: 17
source: dbSNP
start: 73361802
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361804
feature_type: variation
id: rs1363517541
seq_region_name: 17
source: dbSNP
start: 73361804
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361805
feature_type: variation
id: rs775350553
seq_region_name: 17
source: dbSNP
start: 73361805
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361806
feature_type: variation
id: rs760328400
seq_region_name: 17
source: dbSNP
start: 73361806
strand: 1
-
alleles:
- TGTTCCCCTT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73361816
feature_type: variation
id: rs2145422528
seq_region_name: 17
source: dbSNP
start: 73361807
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361808
feature_type: variation
id: rs1351987754
seq_region_name: 17
source: dbSNP
start: 73361808
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361811
feature_type: variation
id: rs776391778
seq_region_name: 17
source: dbSNP
start: 73361811
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361813
feature_type: variation
id: rs897841795
seq_region_name: 17
source: dbSNP
start: 73361813
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361814
feature_type: variation
id: rs761776245
seq_region_name: 17
source: dbSNP
start: 73361814
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361817
feature_type: variation
id: rs1316789626
seq_region_name: 17
source: dbSNP
start: 73361817
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361819
feature_type: variation
id: rs143420601
seq_region_name: 17
source: dbSNP
start: 73361819
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361820
feature_type: variation
id: rs759674807
seq_region_name: 17
source: dbSNP
start: 73361820
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361823
feature_type: variation
id: rs2062643612
seq_region_name: 17
source: dbSNP
start: 73361823
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73361825
feature_type: variation
id: rs147983543
seq_region_name: 17
source: dbSNP
start: 73361825
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361826
feature_type: variation
id: rs760996868
seq_region_name: 17
source: dbSNP
start: 73361826
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361827
feature_type: variation
id: rs752934070
seq_region_name: 17
source: dbSNP
start: 73361827
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361829
feature_type: variation
id: rs1481780487
seq_region_name: 17
source: dbSNP
start: 73361829
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361831
feature_type: variation
id: rs756388184
seq_region_name: 17
source: dbSNP
start: 73361831
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361832
feature_type: variation
id: rs575452411
seq_region_name: 17
source: dbSNP
start: 73361832
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73361835
feature_type: variation
id: rs1424283706
seq_region_name: 17
source: dbSNP
start: 73361835
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73361844
feature_type: variation
id: rs757761646
seq_region_name: 17
source: dbSNP
start: 73361844
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73361845
feature_type: variation
id: rs779621913
seq_region_name: 17
source: dbSNP
start: 73361845
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73361848
feature_type: variation
id: rs113200409
seq_region_name: 17
source: dbSNP
start: 73361848
strand: 1
-
alleles:
- GGGGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73361852
feature_type: variation
id: rs1266124363
seq_region_name: 17
source: dbSNP
start: 73361848
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73361851
feature_type: variation
id: rs771720473
seq_region_name: 17
source: dbSNP
start: 73361851
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73361854
feature_type: variation
id: rs1372003819
seq_region_name: 17
source: dbSNP
start: 73361854
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73361855
feature_type: variation
id: rs1439582488
seq_region_name: 17
source: dbSNP
start: 73361855
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73361861
feature_type: variation
id: rs1297047037
seq_region_name: 17
source: dbSNP
start: 73361861
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361864
feature_type: variation
id: rs1379307536
seq_region_name: 17
source: dbSNP
start: 73361864
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361869
feature_type: variation
id: rs1255790106
seq_region_name: 17
source: dbSNP
start: 73361869
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361872
feature_type: variation
id: rs1397076233
seq_region_name: 17
source: dbSNP
start: 73361872
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361873
feature_type: variation
id: rs1317755433
seq_region_name: 17
source: dbSNP
start: 73361873
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361875
feature_type: variation
id: rs1357981435
seq_region_name: 17
source: dbSNP
start: 73361875
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361876
feature_type: variation
id: rs564167432
seq_region_name: 17
source: dbSNP
start: 73361876
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361877
feature_type: variation
id: rs2145422743
seq_region_name: 17
source: dbSNP
start: 73361877
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361878
feature_type: variation
id: rs2062644275
seq_region_name: 17
source: dbSNP
start: 73361878
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361882
feature_type: variation
id: rs879764318
seq_region_name: 17
source: dbSNP
start: 73361882
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361886
feature_type: variation
id: rs2145422757
seq_region_name: 17
source: dbSNP
start: 73361886
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361887
feature_type: variation
id: rs2062644318
seq_region_name: 17
source: dbSNP
start: 73361887
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361888
feature_type: variation
id: rs746704327
seq_region_name: 17
source: dbSNP
start: 73361888
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361889
feature_type: variation
id: rs143440601
seq_region_name: 17
source: dbSNP
start: 73361889
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361891
feature_type: variation
id: rs776462343
seq_region_name: 17
source: dbSNP
start: 73361891
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361894
feature_type: variation
id: rs757823261
seq_region_name: 17
source: dbSNP
start: 73361894
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361896
feature_type: variation
id: rs150500647
seq_region_name: 17
source: dbSNP
start: 73361896
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361899
feature_type: variation
id: rs887530519
seq_region_name: 17
source: dbSNP
start: 73361899
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361906
feature_type: variation
id: rs11657033
seq_region_name: 17
source: dbSNP
start: 73361906
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361907
feature_type: variation
id: rs1304474201
seq_region_name: 17
source: dbSNP
start: 73361907
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361912
feature_type: variation
id: rs2062644612
seq_region_name: 17
source: dbSNP
start: 73361912
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361913
feature_type: variation
id: rs1033359497
seq_region_name: 17
source: dbSNP
start: 73361913
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361915
feature_type: variation
id: rs2062644663
seq_region_name: 17
source: dbSNP
start: 73361915
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361916
feature_type: variation
id: rs2062644683
seq_region_name: 17
source: dbSNP
start: 73361916
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361920
feature_type: variation
id: rs2062644707
seq_region_name: 17
source: dbSNP
start: 73361920
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361921
feature_type: variation
id: rs1171321003
seq_region_name: 17
source: dbSNP
start: 73361921
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361922
feature_type: variation
id: rs377129708
seq_region_name: 17
source: dbSNP
start: 73361922
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361923
feature_type: variation
id: rs370248334
seq_region_name: 17
source: dbSNP
start: 73361923
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361924
feature_type: variation
id: rs1376539819
seq_region_name: 17
source: dbSNP
start: 73361924
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73361925
feature_type: variation
id: rs1286926902
seq_region_name: 17
source: dbSNP
start: 73361925
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
-
alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
- CGGCTCCATGGTTC
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73362071
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73362100
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73362104
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73362106
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362109
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362114
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73362124
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362125
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362127
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362128
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362130
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362131
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362134
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs745844567
seq_region_name: 17
source: dbSNP
start: 73362135
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1414755165
seq_region_name: 17
source: dbSNP
start: 73362138
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062646947
seq_region_name: 17
source: dbSNP
start: 73362142
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1177982214
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs769692740
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73362197
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362202
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73362204
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs896180418
seq_region_name: 17
source: dbSNP
start: 73362205
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362207
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362209
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362213
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362214
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362215
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362250
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362256
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362258
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362270
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362271
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73362272
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362273
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362279
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362283
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362285
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362288
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362297
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362300
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362300
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362301
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362304
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1452366277
seq_region_name: 17
source: dbSNP
start: 73362305
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs929295428
seq_region_name: 17
source: dbSNP
start: 73362306
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362309
feature_type: variation
id: rs903437297
seq_region_name: 17
source: dbSNP
start: 73362309
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362311
feature_type: variation
id: rs2145423592
seq_region_name: 17
source: dbSNP
start: 73362311
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1197079875
seq_region_name: 17
source: dbSNP
start: 73362312
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362317
feature_type: variation
id: rs999039610
seq_region_name: 17
source: dbSNP
start: 73362317
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568365997
seq_region_name: 17
source: dbSNP
start: 73362318
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362321
feature_type: variation
id: rs2062648420
seq_region_name: 17
source: dbSNP
start: 73362321
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1259262365
seq_region_name: 17
source: dbSNP
start: 73362324
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062648478
seq_region_name: 17
source: dbSNP
start: 73362326
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362332
feature_type: variation
id: rs1216889817
seq_region_name: 17
source: dbSNP
start: 73362332
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062648514
seq_region_name: 17
source: dbSNP
start: 73362335
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362345
feature_type: variation
id: rs1363424768
seq_region_name: 17
source: dbSNP
start: 73362345
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145423630
seq_region_name: 17
source: dbSNP
start: 73362350
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362356
feature_type: variation
id: rs767979099
seq_region_name: 17
source: dbSNP
start: 73362355
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362359
feature_type: variation
id: rs2062648584
seq_region_name: 17
source: dbSNP
start: 73362359
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362365
feature_type: variation
id: rs1049519055
seq_region_name: 17
source: dbSNP
start: 73362365
strand: 1
-
alleles:
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- AGGAGGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362371
feature_type: variation
id: rs1033152069
seq_region_name: 17
source: dbSNP
start: 73362367
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362368
feature_type: variation
id: rs957520295
seq_region_name: 17
source: dbSNP
start: 73362368
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362381
feature_type: variation
id: rs2062648679
seq_region_name: 17
source: dbSNP
start: 73362381
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362383
feature_type: variation
id: rs887802515
seq_region_name: 17
source: dbSNP
start: 73362383
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362385
feature_type: variation
id: rs938243051
seq_region_name: 17
source: dbSNP
start: 73362385
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362386
feature_type: variation
id: rs1055417931
seq_region_name: 17
source: dbSNP
start: 73362386
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362388
feature_type: variation
id: rs2062648767
seq_region_name: 17
source: dbSNP
start: 73362388
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362390
feature_type: variation
id: rs1444217423
seq_region_name: 17
source: dbSNP
start: 73362390
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362394
feature_type: variation
id: rs1171235948
seq_region_name: 17
source: dbSNP
start: 73362394
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362403
feature_type: variation
id: rs1599485028
seq_region_name: 17
source: dbSNP
start: 73362403
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362404
feature_type: variation
id: rs1171036600
seq_region_name: 17
source: dbSNP
start: 73362404
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362405
feature_type: variation
id: rs1205054346
seq_region_name: 17
source: dbSNP
start: 73362405
strand: 1
-
alleles:
- "-"
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alleles:
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-
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362572
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73362573
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362595
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73362610
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362611
strand: 1
-
alleles:
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- AACAAC
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73362612
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73362614
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362615
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362629
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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end: 73362630
feature_type: variation
id: rs1319680653
seq_region_name: 17
source: dbSNP
start: 73362630
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362632
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362633
feature_type: variation
id: rs1288930369
seq_region_name: 17
source: dbSNP
start: 73362632
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73362808
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362812
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73362814
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73362819
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362820
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73362821
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362823
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362824
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362827
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362828
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1159595981
seq_region_name: 17
source: dbSNP
start: 73362830
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1171843190
seq_region_name: 17
source: dbSNP
start: 73362831
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362831
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73362840
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362841
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362842
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362843
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362846
feature_type: variation
id: rs1251918516
seq_region_name: 17
source: dbSNP
start: 73362843
strand: 1
-
alleles:
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- GGTTAGGTTAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362850
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73362845
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1236183869
seq_region_name: 17
source: dbSNP
start: 73362846
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1195121937
seq_region_name: 17
source: dbSNP
start: 73362852
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73362856
feature_type: variation
id: rs1599485445
seq_region_name: 17
source: dbSNP
start: 73362856
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- CAG
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73363018
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73363019
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363021
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363037
strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73363038
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363042
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363047
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363048
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363050
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363051
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363060
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363061
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363062
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs756121767
seq_region_name: 17
source: dbSNP
start: 73363068
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363074
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363077
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1206004618
seq_region_name: 17
source: dbSNP
start: 73363079
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363080
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062654940
seq_region_name: 17
source: dbSNP
start: 73363084
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1264090644
seq_region_name: 17
source: dbSNP
start: 73363085
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363086
feature_type: variation
id: rs1233086333
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source: dbSNP
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062655281
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs555650922
seq_region_name: 17
source: dbSNP
start: 73363146
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363147
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062655408
seq_region_name: 17
source: dbSNP
start: 73363153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1241646433
seq_region_name: 17
source: dbSNP
start: 73363159
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs576416380
seq_region_name: 17
source: dbSNP
start: 73363160
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062655483
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363172
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062655710
seq_region_name: 17
source: dbSNP
start: 73363173
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363175
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363176
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363180
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363185
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs562622677
seq_region_name: 17
source: dbSNP
start: 73363186
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062655903
seq_region_name: 17
source: dbSNP
start: 73363187
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363190
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363192
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363193
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363197
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363201
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363203
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1327774446
seq_region_name: 17
source: dbSNP
start: 73363204
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs778596288
seq_region_name: 17
source: dbSNP
start: 73363208
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs377484922
seq_region_name: 17
source: dbSNP
start: 73363209
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs747804481
seq_region_name: 17
source: dbSNP
start: 73363210
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599485701
seq_region_name: 17
source: dbSNP
start: 73363211
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1599485705
seq_region_name: 17
source: dbSNP
start: 73363212
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs544997723
seq_region_name: 17
source: dbSNP
start: 73363216
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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id: rs771560307
seq_region_name: 17
source: dbSNP
start: 73363217
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062656366
seq_region_name: 17
source: dbSNP
start: 73363219
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1418747213
seq_region_name: 17
source: dbSNP
start: 73363220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs990925474
seq_region_name: 17
source: dbSNP
start: 73363222
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363223
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1476438658
seq_region_name: 17
source: dbSNP
start: 73363227
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062656496
seq_region_name: 17
source: dbSNP
start: 73363229
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs572406222
seq_region_name: 17
source: dbSNP
start: 73363230
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1006285018
seq_region_name: 17
source: dbSNP
start: 73363231
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73363238
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363238
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363242
feature_type: variation
id: rs2062656609
seq_region_name: 17
source: dbSNP
start: 73363242
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062656641
seq_region_name: 17
source: dbSNP
start: 73363252
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062656663
seq_region_name: 17
source: dbSNP
start: 73363255
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363258
feature_type: variation
id: rs1469174219
seq_region_name: 17
source: dbSNP
start: 73363258
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363265
feature_type: variation
id: rs2145425601
seq_region_name: 17
source: dbSNP
start: 73363265
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363268
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2145425606
seq_region_name: 17
source: dbSNP
start: 73363271
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363272
feature_type: variation
id: rs541283649
seq_region_name: 17
source: dbSNP
start: 73363272
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363273
feature_type: variation
id: rs187476370
seq_region_name: 17
source: dbSNP
start: 73363273
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363274
feature_type: variation
id: rs2062656795
seq_region_name: 17
source: dbSNP
start: 73363274
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363277
feature_type: variation
id: rs1274341466
seq_region_name: 17
source: dbSNP
start: 73363277
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363288
feature_type: variation
id: rs1406000682
seq_region_name: 17
source: dbSNP
start: 73363288
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363290
feature_type: variation
id: rs2062656853
seq_region_name: 17
source: dbSNP
start: 73363290
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363291
feature_type: variation
id: rs1300789416
seq_region_name: 17
source: dbSNP
start: 73363291
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363293
feature_type: variation
id: rs2062656896
seq_region_name: 17
source: dbSNP
start: 73363293
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363301
feature_type: variation
id: rs2062656914
seq_region_name: 17
source: dbSNP
start: 73363301
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363302
feature_type: variation
id: rs2062656940
seq_region_name: 17
source: dbSNP
start: 73363302
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363307
feature_type: variation
id: rs139953110
seq_region_name: 17
source: dbSNP
start: 73363307
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363311
feature_type: variation
id: rs1764563839
seq_region_name: 17
source: dbSNP
start: 73363311
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363315
feature_type: variation
id: rs1371422281
seq_region_name: 17
source: dbSNP
start: 73363315
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73363316
feature_type: variation
id: rs771441129
seq_region_name: 17
source: dbSNP
start: 73363316
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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start: 73363536
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73363546
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73363556
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73363559
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363560
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73363561
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363572
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363783
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363784
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363794
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73363796
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73363798
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363802
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062661231
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73363808
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1268673436
seq_region_name: 17
source: dbSNP
start: 73363809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363813
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73363814
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73363815
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1000043875
seq_region_name: 17
source: dbSNP
start: 73363822
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73364018
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73364022
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73364023
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73364026
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364030
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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-
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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source: dbSNP
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs754778756
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364172
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364177
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364180
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364181
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73364184
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145427522
seq_region_name: 17
source: dbSNP
start: 73364190
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364191
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364200
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364201
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364202
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1395923881
seq_region_name: 17
source: dbSNP
start: 73364204
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1168677241
seq_region_name: 17
source: dbSNP
start: 73364205
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs935164942
seq_region_name: 17
source: dbSNP
start: 73364207
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1451515512
seq_region_name: 17
source: dbSNP
start: 73364213
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145427577
seq_region_name: 17
source: dbSNP
start: 73364214
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062665047
seq_region_name: 17
source: dbSNP
start: 73364215
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1393517017
seq_region_name: 17
source: dbSNP
start: 73364216
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364218
feature_type: variation
id: rs2062665107
seq_region_name: 17
source: dbSNP
start: 73364218
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364219
feature_type: variation
id: rs1568366763
seq_region_name: 17
source: dbSNP
start: 73364219
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062665156
seq_region_name: 17
source: dbSNP
start: 73364220
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062665177
seq_region_name: 17
source: dbSNP
start: 73364221
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1211382381
seq_region_name: 17
source: dbSNP
start: 73364226
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364227
feature_type: variation
id: rs1052506514
seq_region_name: 17
source: dbSNP
start: 73364227
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364229
feature_type: variation
id: rs1459984550
seq_region_name: 17
source: dbSNP
start: 73364229
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364231
feature_type: variation
id: rs1599486485
seq_region_name: 17
source: dbSNP
start: 73364231
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364233
feature_type: variation
id: rs2145427627
seq_region_name: 17
source: dbSNP
start: 73364233
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364236
feature_type: variation
id: rs747795657
seq_region_name: 17
source: dbSNP
start: 73364236
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062665304
seq_region_name: 17
source: dbSNP
start: 73364241
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364246
feature_type: variation
id: rs1599486495
seq_region_name: 17
source: dbSNP
start: 73364246
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364247
feature_type: variation
id: rs1180354062
seq_region_name: 17
source: dbSNP
start: 73364247
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364249
feature_type: variation
id: rs1435540699
seq_region_name: 17
source: dbSNP
start: 73364249
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364250
feature_type: variation
id: rs2062665375
seq_region_name: 17
source: dbSNP
start: 73364250
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364251
feature_type: variation
id: rs1271633620
seq_region_name: 17
source: dbSNP
start: 73364251
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364253
feature_type: variation
id: rs1010973638
seq_region_name: 17
source: dbSNP
start: 73364253
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364256
feature_type: variation
id: rs1203132577
seq_region_name: 17
source: dbSNP
start: 73364256
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73364410
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alleles:
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assembly_name: GRCh38
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start: 73364411
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364428
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73364430
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73364442
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364445
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73364452
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73364454
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364457
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73364458
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364462
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364464
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364465
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364471
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364473
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364483
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364488
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364705
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73364710
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73364712
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73364714
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73364717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364723
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364724
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364725
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364726
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364728
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364746
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364749
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364750
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364754
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364765
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364768
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73364913
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2062671080
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73364924
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364926
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364928
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73364929
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364932
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73364934
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73364946
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs538470739
seq_region_name: 17
source: dbSNP
start: 73364953
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364956
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364959
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73364960
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062671383
seq_region_name: 17
source: dbSNP
start: 73364962
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1339442725
seq_region_name: 17
source: dbSNP
start: 73364963
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062671435
seq_region_name: 17
source: dbSNP
start: 73364964
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1334476995
seq_region_name: 17
source: dbSNP
start: 73364965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs904928951
seq_region_name: 17
source: dbSNP
start: 73364966
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs774777990
seq_region_name: 17
source: dbSNP
start: 73364968
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1382563672
seq_region_name: 17
source: dbSNP
start: 73364974
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1035093940
seq_region_name: 17
source: dbSNP
start: 73364977
strand: 1
-
alleles:
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- CCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364985
feature_type: variation
id: rs1384224619
seq_region_name: 17
source: dbSNP
start: 73364979
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs184461393
seq_region_name: 17
source: dbSNP
start: 73364980
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364985
feature_type: variation
id: rs2062671615
seq_region_name: 17
source: dbSNP
start: 73364984
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73364985
feature_type: variation
id: rs2145429211
seq_region_name: 17
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start: 73364985
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365110
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365119
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365129
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73365131
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365132
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365135
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365135
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1201241920
seq_region_name: 17
source: dbSNP
start: 73365138
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365144
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365144
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365148
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365150
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365151
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1228855360
seq_region_name: 17
source: dbSNP
start: 73365152
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs563058441
seq_region_name: 17
source: dbSNP
start: 73365158
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1272973695
seq_region_name: 17
source: dbSNP
start: 73365159
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1435618972
seq_region_name: 17
source: dbSNP
start: 73365160
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365164
strand: 1
-
alleles:
- CAC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1331630516
seq_region_name: 17
source: dbSNP
start: 73365166
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365168
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365170
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062673205
seq_region_name: 17
source: dbSNP
start: 73365171
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365172
feature_type: variation
id: rs1408082809
seq_region_name: 17
source: dbSNP
start: 73365171
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365172
feature_type: variation
id: rs1272195422
seq_region_name: 17
source: dbSNP
start: 73365172
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365173
feature_type: variation
id: rs1044938607
seq_region_name: 17
source: dbSNP
start: 73365173
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365175
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365178
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062673353
seq_region_name: 17
source: dbSNP
start: 73365181
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365182
feature_type: variation
id: rs907406148
seq_region_name: 17
source: dbSNP
start: 73365182
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365183
feature_type: variation
id: rs1468944839
seq_region_name: 17
source: dbSNP
start: 73365183
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365185
feature_type: variation
id: rs578178091
seq_region_name: 17
source: dbSNP
start: 73365185
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365186
feature_type: variation
id: rs1393615935
seq_region_name: 17
source: dbSNP
start: 73365186
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365188
feature_type: variation
id: rs1056638512
seq_region_name: 17
source: dbSNP
start: 73365188
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365189
feature_type: variation
id: rs1003693939
seq_region_name: 17
source: dbSNP
start: 73365189
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365190
feature_type: variation
id: rs545623622
seq_region_name: 17
source: dbSNP
start: 73365190
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062673557
seq_region_name: 17
source: dbSNP
start: 73365191
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365192
feature_type: variation
id: rs376530575
seq_region_name: 17
source: dbSNP
start: 73365192
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365193
feature_type: variation
id: rs144055454
seq_region_name: 17
source: dbSNP
start: 73365193
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365194
feature_type: variation
id: rs879150049
seq_region_name: 17
source: dbSNP
start: 73365194
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365195
feature_type: variation
id: rs2145429659
seq_region_name: 17
source: dbSNP
start: 73365195
strand: 1
-
alleles:
- TGAGATGAGA
- TGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365204
feature_type: variation
id: rs1470990067
seq_region_name: 17
source: dbSNP
start: 73365195
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365196
feature_type: variation
id: rs1250589794
seq_region_name: 17
source: dbSNP
start: 73365196
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365199
feature_type: variation
id: rs1205482719
seq_region_name: 17
source: dbSNP
start: 73365199
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365200
feature_type: variation
id: rs1343891916
seq_region_name: 17
source: dbSNP
start: 73365200
strand: 1
-
alleles:
- TG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365201
feature_type: variation
id: rs2062673781
seq_region_name: 17
source: dbSNP
start: 73365200
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365201
feature_type: variation
id: rs903954353
seq_region_name: 17
source: dbSNP
start: 73365201
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365206
feature_type: variation
id: rs1009205605
seq_region_name: 17
source: dbSNP
start: 73365206
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365207
feature_type: variation
id: rs1022139139
seq_region_name: 17
source: dbSNP
start: 73365207
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365209
feature_type: variation
id: rs2145429719
seq_region_name: 17
source: dbSNP
start: 73365209
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365211
feature_type: variation
id: rs1276616456
seq_region_name: 17
source: dbSNP
start: 73365211
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365216
feature_type: variation
id: rs1226637111
seq_region_name: 17
source: dbSNP
start: 73365216
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365219
feature_type: variation
id: rs1350005322
seq_region_name: 17
source: dbSNP
start: 73365219
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365220
feature_type: variation
id: rs527829527
seq_region_name: 17
source: dbSNP
start: 73365220
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365222
feature_type: variation
id: rs549496670
seq_region_name: 17
source: dbSNP
start: 73365222
strand: 1
-
alleles:
- GGGGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365227
feature_type: variation
id: rs779374562
seq_region_name: 17
source: dbSNP
start: 73365222
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365223
feature_type: variation
id: rs759558164
seq_region_name: 17
source: dbSNP
start: 73365223
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365227
feature_type: variation
id: rs767610921
seq_region_name: 17
source: dbSNP
start: 73365227
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365230
feature_type: variation
id: rs201925266
seq_region_name: 17
source: dbSNP
start: 73365230
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365232
feature_type: variation
id: rs1421400945
seq_region_name: 17
source: dbSNP
start: 73365232
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365235
feature_type: variation
id: rs531591899
seq_region_name: 17
source: dbSNP
start: 73365235
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365238
feature_type: variation
id: rs1157646841
seq_region_name: 17
source: dbSNP
start: 73365238
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365239
feature_type: variation
id: rs753485238
seq_region_name: 17
source: dbSNP
start: 73365239
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365240
feature_type: variation
id: rs201224103
seq_region_name: 17
source: dbSNP
start: 73365240
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365241
feature_type: variation
id: rs746281114
seq_region_name: 17
source: dbSNP
start: 73365241
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365242
feature_type: variation
id: rs79822986
seq_region_name: 17
source: dbSNP
start: 73365242
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365243
feature_type: variation
id: rs760923140
seq_region_name: 17
source: dbSNP
start: 73365243
strand: 1
-
alleles:
- GGGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365248
feature_type: variation
id: rs758645966
seq_region_name: 17
source: dbSNP
start: 73365243
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365245
feature_type: variation
id: rs1169338956
seq_region_name: 17
source: dbSNP
start: 73365245
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365247
feature_type: variation
id: rs2062674341
seq_region_name: 17
source: dbSNP
start: 73365247
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365248
feature_type: variation
id: rs764273480
seq_region_name: 17
source: dbSNP
start: 73365248
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365249
feature_type: variation
id: rs2145429866
seq_region_name: 17
source: dbSNP
start: 73365249
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365264
feature_type: variation
id: rs571472628
seq_region_name: 17
source: dbSNP
start: 73365264
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365265
feature_type: variation
id: rs142027922
seq_region_name: 17
source: dbSNP
start: 73365265
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365267
feature_type: variation
id: rs1209162489
seq_region_name: 17
source: dbSNP
start: 73365267
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365270
feature_type: variation
id: rs765774263
seq_region_name: 17
source: dbSNP
start: 73365270
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365271
feature_type: variation
id: rs1452566251
seq_region_name: 17
source: dbSNP
start: 73365271
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365272
feature_type: variation
id: rs908645252
seq_region_name: 17
source: dbSNP
start: 73365272
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365273
feature_type: variation
id: rs1298742748
seq_region_name: 17
source: dbSNP
start: 73365273
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365277
feature_type: variation
id: rs2062674610
seq_region_name: 17
source: dbSNP
start: 73365277
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365279
feature_type: variation
id: rs145893156
seq_region_name: 17
source: dbSNP
start: 73365279
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365280
feature_type: variation
id: rs757942205
seq_region_name: 17
source: dbSNP
start: 73365280
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365281
feature_type: variation
id: rs1325263279
seq_region_name: 17
source: dbSNP
start: 73365281
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365282
feature_type: variation
id: rs779679666
seq_region_name: 17
source: dbSNP
start: 73365282
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365283
feature_type: variation
id: rs1313063947
seq_region_name: 17
source: dbSNP
start: 73365283
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365284
feature_type: variation
id: rs199865242
seq_region_name: 17
source: dbSNP
start: 73365284
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365291
feature_type: variation
id: rs754641798
seq_region_name: 17
source: dbSNP
start: 73365291
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365292
feature_type: variation
id: rs780772270
seq_region_name: 17
source: dbSNP
start: 73365292
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365296
feature_type: variation
id: rs2062674879
seq_region_name: 17
source: dbSNP
start: 73365296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73365297
feature_type: variation
id: rs138802757
seq_region_name: 17
source: dbSNP
start: 73365297
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365299
feature_type: variation
id: rs1243587248
seq_region_name: 17
source: dbSNP
start: 73365299
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73365300
feature_type: variation
id: rs1328366733
seq_region_name: 17
source: dbSNP
start: 73365300
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365304
feature_type: variation
id: rs1851006003
seq_region_name: 17
source: dbSNP
start: 73365304
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365306
feature_type: variation
id: rs1377239231
seq_region_name: 17
source: dbSNP
start: 73365306
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365311
feature_type: variation
id: rs142823039
seq_region_name: 17
source: dbSNP
start: 73365311
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365314
feature_type: variation
id: rs1185759415
seq_region_name: 17
source: dbSNP
start: 73365314
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365315
feature_type: variation
id: rs2062675153
seq_region_name: 17
source: dbSNP
start: 73365315
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365322
feature_type: variation
id: rs370698585
seq_region_name: 17
source: dbSNP
start: 73365322
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365323
feature_type: variation
id: rs1361299109
seq_region_name: 17
source: dbSNP
start: 73365323
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365325
feature_type: variation
id: rs1481247764
seq_region_name: 17
source: dbSNP
start: 73365325
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365326
feature_type: variation
id: rs1318994344
seq_region_name: 17
source: dbSNP
start: 73365326
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365327
feature_type: variation
id: rs1173558622
seq_region_name: 17
source: dbSNP
start: 73365327
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73365329
feature_type: variation
id: rs1457134477
seq_region_name: 17
source: dbSNP
start: 73365328
strand: 1
-
alleles:
- CCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73365332
feature_type: variation
id: rs34566358
seq_region_name: 17
source: dbSNP
start: 73365330
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365338
feature_type: variation
id: rs749258955
seq_region_name: 17
source: dbSNP
start: 73365338
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365340
feature_type: variation
id: rs2145430116
seq_region_name: 17
source: dbSNP
start: 73365340
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365343
feature_type: variation
id: rs770899193
seq_region_name: 17
source: dbSNP
start: 73365343
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365345
feature_type: variation
id: rs374170731
seq_region_name: 17
source: dbSNP
start: 73365345
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365348
feature_type: variation
id: rs2062675431
seq_region_name: 17
source: dbSNP
start: 73365348
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365351
feature_type: variation
id: rs150795175
seq_region_name: 17
source: dbSNP
start: 73365351
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365353
feature_type: variation
id: rs1429053032
seq_region_name: 17
source: dbSNP
start: 73365353
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365355
feature_type: variation
id: rs760723946
seq_region_name: 17
source: dbSNP
start: 73365355
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365358
feature_type: variation
id: rs892722952
seq_region_name: 17
source: dbSNP
start: 73365358
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365361
feature_type: variation
id: rs764375227
seq_region_name: 17
source: dbSNP
start: 73365361
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365366
feature_type: variation
id: rs2062675611
seq_region_name: 17
source: dbSNP
start: 73365366
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365370
feature_type: variation
id: rs776724578
seq_region_name: 17
source: dbSNP
start: 73365370
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365371
feature_type: variation
id: rs1225583102
seq_region_name: 17
source: dbSNP
start: 73365371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365376
feature_type: variation
id: rs138111780
seq_region_name: 17
source: dbSNP
start: 73365376
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365377
feature_type: variation
id: rs765725605
seq_region_name: 17
source: dbSNP
start: 73365377
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365378
feature_type: variation
id: rs149537911
seq_region_name: 17
source: dbSNP
start: 73365378
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365379
feature_type: variation
id: rs758950552
seq_region_name: 17
source: dbSNP
start: 73365379
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365382
feature_type: variation
id: rs766849962
seq_region_name: 17
source: dbSNP
start: 73365382
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365384
feature_type: variation
id: rs1214793044
seq_region_name: 17
source: dbSNP
start: 73365384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365387
feature_type: variation
id: rs144657895
seq_region_name: 17
source: dbSNP
start: 73365387
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73365388
feature_type: variation
id: rs1490719310
seq_region_name: 17
source: dbSNP
start: 73365388
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73365395
feature_type: variation
id: rs377690009
seq_region_name: 17
source: dbSNP
start: 73365395
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73365399
feature_type: variation
id: rs780836188
seq_region_name: 17
source: dbSNP
start: 73365399
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73365400
feature_type: variation
id: rs1472614155
seq_region_name: 17
source: dbSNP
start: 73365400
strand: 1
-
alleles:
- G
- C
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365413
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73365413
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365414
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1028818825
seq_region_name: 17
source: dbSNP
start: 73365416
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365420
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365423
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1366612942
seq_region_name: 17
source: dbSNP
start: 73365424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365425
strand: 1
-
alleles:
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- CTTCT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365429
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs777517177
seq_region_name: 17
source: dbSNP
start: 73365430
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365433
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs938862924
seq_region_name: 17
source: dbSNP
start: 73365434
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365435
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365437
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599487751
seq_region_name: 17
source: dbSNP
start: 73365441
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs369039506
seq_region_name: 17
source: dbSNP
start: 73365444
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145430418
seq_region_name: 17
source: dbSNP
start: 73365447
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs892228932
seq_region_name: 17
source: dbSNP
start: 73365451
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs961300361
seq_region_name: 17
source: dbSNP
start: 73365452
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1386711905
seq_region_name: 17
source: dbSNP
start: 73365454
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs777399901
seq_region_name: 17
source: dbSNP
start: 73365457
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1282584689
seq_region_name: 17
source: dbSNP
start: 73365460
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062676722
seq_region_name: 17
source: dbSNP
start: 73365462
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1248543173
seq_region_name: 17
source: dbSNP
start: 73365464
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062676817
seq_region_name: 17
source: dbSNP
start: 73365466
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062676843
seq_region_name: 17
source: dbSNP
start: 73365467
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365469
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365471
strand: 1
-
alleles:
- TAGCGGGAGTA
- TA
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062676925
seq_region_name: 17
source: dbSNP
start: 73365471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365473
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs945156815
seq_region_name: 17
source: dbSNP
start: 73365474
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365475
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365480
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145430529
seq_region_name: 17
source: dbSNP
start: 73365481
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249249477
seq_region_name: 17
source: dbSNP
start: 73365482
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365484
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1323664607
seq_region_name: 17
source: dbSNP
start: 73365486
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062677109
seq_region_name: 17
source: dbSNP
start: 73365490
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365492
feature_type: variation
id: rs1272841582
seq_region_name: 17
source: dbSNP
start: 73365492
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1338421788
seq_region_name: 17
source: dbSNP
start: 73365494
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1043354213
seq_region_name: 17
source: dbSNP
start: 73365495
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365496
feature_type: variation
id: rs903563816
seq_region_name: 17
source: dbSNP
start: 73365496
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365498
feature_type: variation
id: rs1385556541
seq_region_name: 17
source: dbSNP
start: 73365498
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062677246
seq_region_name: 17
source: dbSNP
start: 73365507
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365509
feature_type: variation
id: rs1270116730
seq_region_name: 17
source: dbSNP
start: 73365509
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs996686236
seq_region_name: 17
source: dbSNP
start: 73365510
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746705147
seq_region_name: 17
source: dbSNP
start: 73365511
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs890931502
seq_region_name: 17
source: dbSNP
start: 73365513
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365515
feature_type: variation
id: rs2062677382
seq_region_name: 17
source: dbSNP
start: 73365515
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365516
feature_type: variation
id: rs756741853
seq_region_name: 17
source: dbSNP
start: 73365516
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1429134535
seq_region_name: 17
source: dbSNP
start: 73365519
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365520
feature_type: variation
id: rs181985986
seq_region_name: 17
source: dbSNP
start: 73365520
strand: 1
-
alleles:
- GGGCGGGC
- GGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365535
feature_type: variation
id: rs912870732
seq_region_name: 17
source: dbSNP
start: 73365528
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365529
feature_type: variation
id: rs1172293624
seq_region_name: 17
source: dbSNP
start: 73365529
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365531
feature_type: variation
id: rs545707719
seq_region_name: 17
source: dbSNP
start: 73365531
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs554454761
seq_region_name: 17
source: dbSNP
start: 73365532
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1026978103
seq_region_name: 17
source: dbSNP
start: 73365534
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365535
feature_type: variation
id: rs1191845458
seq_region_name: 17
source: dbSNP
start: 73365535
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365538
feature_type: variation
id: rs1490878637
seq_region_name: 17
source: dbSNP
start: 73365538
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365542
feature_type: variation
id: rs2062677685
seq_region_name: 17
source: dbSNP
start: 73365542
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365544
feature_type: variation
id: rs1599487879
seq_region_name: 17
source: dbSNP
start: 73365544
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365545
feature_type: variation
id: rs2062677732
seq_region_name: 17
source: dbSNP
start: 73365545
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365547
feature_type: variation
id: rs970052280
seq_region_name: 17
source: dbSNP
start: 73365547
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1204757200
seq_region_name: 17
source: dbSNP
start: 73365551
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365553
feature_type: variation
id: rs143391652
seq_region_name: 17
source: dbSNP
start: 73365553
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365556
feature_type: variation
id: rs1277152258
seq_region_name: 17
source: dbSNP
start: 73365556
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365558
feature_type: variation
id: rs2145430700
seq_region_name: 17
source: dbSNP
start: 73365558
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365561
feature_type: variation
id: rs2062677830
seq_region_name: 17
source: dbSNP
start: 73365561
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365562
feature_type: variation
id: rs2062677846
seq_region_name: 17
source: dbSNP
start: 73365562
strand: 1
-
alleles:
- CCCCCTTCCTCTCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365575
feature_type: variation
id: rs1599487898
seq_region_name: 17
source: dbSNP
start: 73365562
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365565
feature_type: variation
id: rs1231533785
seq_region_name: 17
source: dbSNP
start: 73365565
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365569
feature_type: variation
id: rs2062677912
seq_region_name: 17
source: dbSNP
start: 73365569
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365570
feature_type: variation
id: rs543177830
seq_region_name: 17
source: dbSNP
start: 73365570
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365571
feature_type: variation
id: rs1422545647
seq_region_name: 17
source: dbSNP
start: 73365571
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365583
feature_type: variation
id: rs1568367401
seq_region_name: 17
source: dbSNP
start: 73365583
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365592
feature_type: variation
id: rs2062677998
seq_region_name: 17
source: dbSNP
start: 73365592
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365593
feature_type: variation
id: rs932821474
seq_region_name: 17
source: dbSNP
start: 73365593
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365595
feature_type: variation
id: rs1362646926
seq_region_name: 17
source: dbSNP
start: 73365595
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365599
feature_type: variation
id: rs1049882700
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73365810
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73365813
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73365815
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365818
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365820
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365821
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365828
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365829
strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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-
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73365918
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73365919
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365935
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365941
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73365943
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365944
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365945
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145431592
seq_region_name: 17
source: dbSNP
start: 73365948
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365959
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365959
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365966
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365967
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365968
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365970
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365971
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365976
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365977
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365982
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365983
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1681410801
seq_region_name: 17
source: dbSNP
start: 73365984
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1341377625
seq_region_name: 17
source: dbSNP
start: 73365985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062681568
seq_region_name: 17
source: dbSNP
start: 73365985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062681618
seq_region_name: 17
source: dbSNP
start: 73365987
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145431691
seq_region_name: 17
source: dbSNP
start: 73365988
strand: 1
-
alleles:
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- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73365991
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1232599109
seq_region_name: 17
source: dbSNP
start: 73365992
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365995
feature_type: variation
id: rs2145431706
seq_region_name: 17
source: dbSNP
start: 73365995
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73365998
feature_type: variation
id: rs1002048636
seq_region_name: 17
source: dbSNP
start: 73365998
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366001
feature_type: variation
id: rs1035691811
seq_region_name: 17
source: dbSNP
start: 73366001
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366002
feature_type: variation
id: rs2062681739
seq_region_name: 17
source: dbSNP
start: 73366002
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366004
feature_type: variation
id: rs2062681766
seq_region_name: 17
source: dbSNP
start: 73366004
strand: 1
-
alleles:
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- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366009
feature_type: variation
id: rs763934814
seq_region_name: 17
source: dbSNP
start: 73366005
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366008
feature_type: variation
id: rs985714391
seq_region_name: 17
source: dbSNP
start: 73366008
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366010
feature_type: variation
id: rs543265487
seq_region_name: 17
source: dbSNP
start: 73366010
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366017
feature_type: variation
id: rs9899809
seq_region_name: 17
source: dbSNP
start: 73366017
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366019
feature_type: variation
id: rs1010405863
seq_region_name: 17
source: dbSNP
start: 73366019
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366021
feature_type: variation
id: rs2062681929
seq_region_name: 17
source: dbSNP
start: 73366021
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366023
feature_type: variation
id: rs2062681951
seq_region_name: 17
source: dbSNP
start: 73366023
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366025
feature_type: variation
id: rs2062681985
seq_region_name: 17
source: dbSNP
start: 73366025
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366028
feature_type: variation
id: rs1412061749
seq_region_name: 17
source: dbSNP
start: 73366028
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs2062682369
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062682518
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs139165569
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs565178472
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366105
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1374457929
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568367611
seq_region_name: 17
source: dbSNP
start: 73366109
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366118
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1036924548
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366123
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366125
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1470555666
seq_region_name: 17
source: dbSNP
start: 73366126
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs540958929
seq_region_name: 17
source: dbSNP
start: 73366129
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062683078
seq_region_name: 17
source: dbSNP
start: 73366135
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366136
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1321540575
seq_region_name: 17
source: dbSNP
start: 73366137
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs905729807
seq_region_name: 17
source: dbSNP
start: 73366138
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062683157
seq_region_name: 17
source: dbSNP
start: 73366139
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599488374
seq_region_name: 17
source: dbSNP
start: 73366140
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs9908457
seq_region_name: 17
source: dbSNP
start: 73366143
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1057463633
seq_region_name: 17
source: dbSNP
start: 73366144
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062683286
seq_region_name: 17
source: dbSNP
start: 73366145
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366147
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366148
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1250978001
seq_region_name: 17
source: dbSNP
start: 73366149
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366150
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366150
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs759459118
seq_region_name: 17
source: dbSNP
start: 73366151
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1461661765
seq_region_name: 17
source: dbSNP
start: 73366152
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366155
feature_type: variation
id: rs2062683489
seq_region_name: 17
source: dbSNP
start: 73366155
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1265002670
seq_region_name: 17
source: dbSNP
start: 73366159
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062683534
seq_region_name: 17
source: dbSNP
start: 73366160
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1020271702
seq_region_name: 17
source: dbSNP
start: 73366161
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366162
feature_type: variation
id: rs2145432165
seq_region_name: 17
source: dbSNP
start: 73366162
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366164
feature_type: variation
id: rs968925691
seq_region_name: 17
source: dbSNP
start: 73366164
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366166
feature_type: variation
id: rs1599488412
seq_region_name: 17
source: dbSNP
start: 73366166
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062683627
seq_region_name: 17
source: dbSNP
start: 73366174
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366176
feature_type: variation
id: rs77685205
seq_region_name: 17
source: dbSNP
start: 73366176
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366177
feature_type: variation
id: rs548094505
seq_region_name: 17
source: dbSNP
start: 73366177
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366178
feature_type: variation
id: rs1426525196
seq_region_name: 17
source: dbSNP
start: 73366178
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366178
feature_type: variation
id: rs2062683744
seq_region_name: 17
source: dbSNP
start: 73366178
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366180
feature_type: variation
id: rs1225633159
seq_region_name: 17
source: dbSNP
start: 73366180
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366181
feature_type: variation
id: rs1599488425
seq_region_name: 17
source: dbSNP
start: 73366181
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366183
feature_type: variation
id: rs1377263158
seq_region_name: 17
source: dbSNP
start: 73366183
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366191
feature_type: variation
id: rs2062683838
seq_region_name: 17
source: dbSNP
start: 73366191
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366192
feature_type: variation
id: rs1029101366
seq_region_name: 17
source: dbSNP
start: 73366192
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366195
feature_type: variation
id: rs1413442810
seq_region_name: 17
source: dbSNP
start: 73366195
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366198
feature_type: variation
id: rs2062683882
seq_region_name: 17
source: dbSNP
start: 73366198
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366200
feature_type: variation
id: rs1385598302
seq_region_name: 17
source: dbSNP
start: 73366200
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366201
feature_type: variation
id: rs953073425
seq_region_name: 17
source: dbSNP
start: 73366201
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366203
feature_type: variation
id: rs2062683950
seq_region_name: 17
source: dbSNP
start: 73366203
strand: 1
-
alleles:
- GCCCTTCCTGCC
- GCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366223
feature_type: variation
id: rs2062683975
seq_region_name: 17
source: dbSNP
start: 73366212
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366215
feature_type: variation
id: rs2062684004
seq_region_name: 17
source: dbSNP
start: 73366215
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366221
feature_type: variation
id: rs1568367656
seq_region_name: 17
source: dbSNP
start: 73366221
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366222
feature_type: variation
id: rs2062684037
seq_region_name: 17
source: dbSNP
start: 73366222
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366223
feature_type: variation
id: rs1432227281
seq_region_name: 17
source: dbSNP
start: 73366223
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366224
feature_type: variation
id: rs1344055179
seq_region_name: 17
source: dbSNP
start: 73366224
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366228
feature_type: variation
id: rs2062684103
seq_region_name: 17
source: dbSNP
start: 73366228
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366229
feature_type: variation
id: rs953681454
seq_region_name: 17
source: dbSNP
start: 73366229
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366338
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366366
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366375
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366377
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366379
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366380
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366382
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366392
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366394
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366398
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062685871
seq_region_name: 17
source: dbSNP
start: 73366405
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366406
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366411
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366412
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366420
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366420
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1025305749
seq_region_name: 17
source: dbSNP
start: 73366421
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73366423
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366427
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062686091
seq_region_name: 17
source: dbSNP
start: 73366428
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73366429
feature_type: variation
id: rs1599488636
seq_region_name: 17
source: dbSNP
start: 73366429
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366597
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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start: 73366604
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366611
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366618
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366624
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366636
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366639
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366640
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366650
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366660
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366677
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1282251498
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366865
strand: 1
-
alleles:
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- TCTCCCCTCCCTGCCTCTACTCTCTCCCCTCCCTGCCTCTACTCTCTCCCCTCC
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73366873
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73366874
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73366876
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366877
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366878
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366879
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366886
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366887
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366888
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73366889
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366892
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73366893
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73367106
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73367107
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367113
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367116
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367118
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367120
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367126
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367127
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367128
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73367128
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062691743
seq_region_name: 17
source: dbSNP
start: 73367129
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062691818
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367138
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062691867
seq_region_name: 17
source: dbSNP
start: 73367139
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs919496652
seq_region_name: 17
source: dbSNP
start: 73367141
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367143
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs191980586
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062692045
seq_region_name: 17
source: dbSNP
start: 73367146
strand: 1
-
alleles:
- AAGGGT
- "-"
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs2062692070
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145434224
seq_region_name: 17
source: dbSNP
start: 73367148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692094
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062692143
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs556169441
seq_region_name: 17
source: dbSNP
start: 73367152
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs887423107
seq_region_name: 17
source: dbSNP
start: 73367153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs941661528
seq_region_name: 17
source: dbSNP
start: 73367163
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs887981249
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs556058739
seq_region_name: 17
source: dbSNP
start: 73367167
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692304
seq_region_name: 17
source: dbSNP
start: 73367169
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1415961021
seq_region_name: 17
source: dbSNP
start: 73367173
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1184831799
seq_region_name: 17
source: dbSNP
start: 73367177
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692395
seq_region_name: 17
source: dbSNP
start: 73367179
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692421
seq_region_name: 17
source: dbSNP
start: 73367180
strand: 1
-
alleles:
- TTTTTT
- TTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1255035740
seq_region_name: 17
source: dbSNP
start: 73367182
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1005681825
seq_region_name: 17
source: dbSNP
start: 73367187
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145434315
seq_region_name: 17
source: dbSNP
start: 73367188
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1055554183
seq_region_name: 17
source: dbSNP
start: 73367191
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1277275514
seq_region_name: 17
source: dbSNP
start: 73367194
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692547
seq_region_name: 17
source: dbSNP
start: 73367195
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367196
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692599
seq_region_name: 17
source: dbSNP
start: 73367198
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692626
seq_region_name: 17
source: dbSNP
start: 73367200
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1242803962
seq_region_name: 17
source: dbSNP
start: 73367201
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062692700
seq_region_name: 17
source: dbSNP
start: 73367203
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367205
feature_type: variation
id: rs1482296832
seq_region_name: 17
source: dbSNP
start: 73367205
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367206
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1218148781
seq_region_name: 17
source: dbSNP
start: 73367207
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1489924852
seq_region_name: 17
source: dbSNP
start: 73367209
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367210
feature_type: variation
id: rs2062692809
seq_region_name: 17
source: dbSNP
start: 73367210
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062692835
seq_region_name: 17
source: dbSNP
start: 73367211
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367214
feature_type: variation
id: rs1291410705
seq_region_name: 17
source: dbSNP
start: 73367214
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062692879
seq_region_name: 17
source: dbSNP
start: 73367221
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062692904
seq_region_name: 17
source: dbSNP
start: 73367223
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367226
feature_type: variation
id: rs2062692922
seq_region_name: 17
source: dbSNP
start: 73367226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367229
feature_type: variation
id: rs2062692943
seq_region_name: 17
source: dbSNP
start: 73367229
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367232
feature_type: variation
id: rs1223774510
seq_region_name: 17
source: dbSNP
start: 73367232
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367235
feature_type: variation
id: rs894111717
seq_region_name: 17
source: dbSNP
start: 73367235
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367236
feature_type: variation
id: rs1013932696
seq_region_name: 17
source: dbSNP
start: 73367236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367239
feature_type: variation
id: rs894699695
seq_region_name: 17
source: dbSNP
start: 73367239
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367242
feature_type: variation
id: rs773542099
seq_region_name: 17
source: dbSNP
start: 73367242
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367244
feature_type: variation
id: rs2145434420
seq_region_name: 17
source: dbSNP
start: 73367244
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367245
feature_type: variation
id: rs2145434426
seq_region_name: 17
source: dbSNP
start: 73367245
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367246
feature_type: variation
id: rs1270293961
seq_region_name: 17
source: dbSNP
start: 73367246
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367249
feature_type: variation
id: rs1401405459
seq_region_name: 17
source: dbSNP
start: 73367249
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367250
feature_type: variation
id: rs2062693069
seq_region_name: 17
source: dbSNP
start: 73367250
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367251
feature_type: variation
id: rs1363338849
seq_region_name: 17
source: dbSNP
start: 73367251
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367252
feature_type: variation
id: rs2062693110
seq_region_name: 17
source: dbSNP
start: 73367252
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367253
feature_type: variation
id: rs1014380447
seq_region_name: 17
source: dbSNP
start: 73367253
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367255
feature_type: variation
id: rs1434969131
seq_region_name: 17
source: dbSNP
start: 73367255
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367256
feature_type: variation
id: rs2145434460
seq_region_name: 17
source: dbSNP
start: 73367256
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367257
feature_type: variation
id: rs1351514013
seq_region_name: 17
source: dbSNP
start: 73367257
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367258
feature_type: variation
id: rs903089432
seq_region_name: 17
source: dbSNP
start: 73367258
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367260
feature_type: variation
id: rs1168180011
seq_region_name: 17
source: dbSNP
start: 73367260
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367261
feature_type: variation
id: rs1409323969
seq_region_name: 17
source: dbSNP
start: 73367261
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367264
feature_type: variation
id: rs2145434491
seq_region_name: 17
source: dbSNP
start: 73367264
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367269
feature_type: variation
id: rs998766464
seq_region_name: 17
source: dbSNP
start: 73367269
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367272
feature_type: variation
id: rs2145434497
seq_region_name: 17
source: dbSNP
start: 73367272
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367273
feature_type: variation
id: rs1420238400
seq_region_name: 17
source: dbSNP
start: 73367273
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367277
feature_type: variation
id: rs534786608
seq_region_name: 17
source: dbSNP
start: 73367277
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367279
feature_type: variation
id: rs2062693359
seq_region_name: 17
source: dbSNP
start: 73367279
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367280
feature_type: variation
id: rs1599489368
seq_region_name: 17
source: dbSNP
start: 73367280
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367283
feature_type: variation
id: rs2062693403
seq_region_name: 17
source: dbSNP
start: 73367283
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367284
feature_type: variation
id: rs576109386
seq_region_name: 17
source: dbSNP
start: 73367284
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367288
feature_type: variation
id: rs2062693462
seq_region_name: 17
source: dbSNP
start: 73367288
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367289
feature_type: variation
id: rs2062693489
seq_region_name: 17
source: dbSNP
start: 73367289
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367294
feature_type: variation
id: rs2062693502
seq_region_name: 17
source: dbSNP
start: 73367294
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367295
feature_type: variation
id: rs7223979
seq_region_name: 17
source: dbSNP
start: 73367295
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367300
feature_type: variation
id: rs2062693588
seq_region_name: 17
source: dbSNP
start: 73367300
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367302
feature_type: variation
id: rs2062693603
seq_region_name: 17
source: dbSNP
start: 73367302
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367303
feature_type: variation
id: rs2062693625
seq_region_name: 17
source: dbSNP
start: 73367303
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367307
feature_type: variation
id: rs2062693653
seq_region_name: 17
source: dbSNP
start: 73367307
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367308
feature_type: variation
id: rs1033035215
seq_region_name: 17
source: dbSNP
start: 73367308
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367310
feature_type: variation
id: rs1017705918
seq_region_name: 17
source: dbSNP
start: 73367310
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367311
feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062693835
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- CCCCA
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367348
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73367349
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs975926900
seq_region_name: 17
source: dbSNP
start: 73367357
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs775268422
seq_region_name: 17
source: dbSNP
start: 73367358
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367366
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367368
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367369
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs183657880
seq_region_name: 17
source: dbSNP
start: 73367372
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367375
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367377
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367380
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367381
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs763838452
seq_region_name: 17
source: dbSNP
start: 73367384
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145434812
seq_region_name: 17
source: dbSNP
start: 73367386
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367387
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs929063735
seq_region_name: 17
source: dbSNP
start: 73367393
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367397
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367400
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367403
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367405
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599489495
seq_region_name: 17
source: dbSNP
start: 73367409
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367413
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs937684827
seq_region_name: 17
source: dbSNP
start: 73367414
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1313590171
seq_region_name: 17
source: dbSNP
start: 73367415
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367420
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145434894
seq_region_name: 17
source: dbSNP
start: 73367421
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367425
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1304593134
seq_region_name: 17
source: dbSNP
start: 73367427
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599489520
seq_region_name: 17
source: dbSNP
start: 73367429
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367430
feature_type: variation
id: rs998694462
seq_region_name: 17
source: dbSNP
start: 73367430
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs761401107
seq_region_name: 17
source: dbSNP
start: 73367434
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1340409228
seq_region_name: 17
source: dbSNP
start: 73367435
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs892936531
seq_region_name: 17
source: dbSNP
start: 73367436
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062694926
seq_region_name: 17
source: dbSNP
start: 73367437
strand: 1
-
alleles:
- C
- CAAAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs916184281
seq_region_name: 17
source: dbSNP
start: 73367440
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062694944
seq_region_name: 17
source: dbSNP
start: 73367440
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062695000
seq_region_name: 17
source: dbSNP
start: 73367445
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062695023
seq_region_name: 17
source: dbSNP
start: 73367450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145434956
seq_region_name: 17
source: dbSNP
start: 73367452
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367453
feature_type: variation
id: rs1405379807
seq_region_name: 17
source: dbSNP
start: 73367453
strand: 1
-
alleles:
- CCCCC
- CCCC
- CCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1450399640
seq_region_name: 17
source: dbSNP
start: 73367453
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1204970487
seq_region_name: 17
source: dbSNP
start: 73367454
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293137256
seq_region_name: 17
source: dbSNP
start: 73367457
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs750226107
seq_region_name: 17
source: dbSNP
start: 73367459
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599489569
seq_region_name: 17
source: dbSNP
start: 73367461
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1362351822
seq_region_name: 17
source: dbSNP
start: 73367464
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367468
feature_type: variation
id: rs1489779360
seq_region_name: 17
source: dbSNP
start: 73367468
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062695256
seq_region_name: 17
source: dbSNP
start: 73367470
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367471
feature_type: variation
id: rs1599489581
seq_region_name: 17
source: dbSNP
start: 73367471
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367476
feature_type: variation
id: rs950271234
seq_region_name: 17
source: dbSNP
start: 73367476
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062695327
seq_region_name: 17
source: dbSNP
start: 73367480
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367482
feature_type: variation
id: rs2062695352
seq_region_name: 17
source: dbSNP
start: 73367482
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367487
feature_type: variation
id: rs2145435044
seq_region_name: 17
source: dbSNP
start: 73367487
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367488
feature_type: variation
id: rs767068803
seq_region_name: 17
source: dbSNP
start: 73367488
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367490
feature_type: variation
id: rs1420106903
seq_region_name: 17
source: dbSNP
start: 73367490
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367492
feature_type: variation
id: rs2062695416
seq_region_name: 17
source: dbSNP
start: 73367492
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367494
feature_type: variation
id: rs2062695432
seq_region_name: 17
source: dbSNP
start: 73367494
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367497
feature_type: variation
id: rs1599489593
seq_region_name: 17
source: dbSNP
start: 73367497
strand: 1
-
alleles:
- TCTTGTCTT
- TCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367507
feature_type: variation
id: rs1382582766
seq_region_name: 17
source: dbSNP
start: 73367499
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367500
feature_type: variation
id: rs2062695497
seq_region_name: 17
source: dbSNP
start: 73367500
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367501
feature_type: variation
id: rs2062695521
seq_region_name: 17
source: dbSNP
start: 73367501
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367504
feature_type: variation
id: rs1182229685
seq_region_name: 17
source: dbSNP
start: 73367504
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367505
feature_type: variation
id: rs2062695587
seq_region_name: 17
source: dbSNP
start: 73367505
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367506
feature_type: variation
id: rs1599489609
seq_region_name: 17
source: dbSNP
start: 73367506
strand: 1
-
alleles:
- TTTTTTTTTTTT
- TTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTTT
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73367875
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73367876
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367877
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73367878
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73367882
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73367887
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367889
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367896
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367899
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367900
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367914
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367915
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367917
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367919
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367920
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367924
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367933
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367934
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367934
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367937
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73367937
strand: 1
-
alleles:
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- ACTTGCTTATACTTGCTTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73367948
feature_type: variation
id: rs2062699510
seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73368118
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73368126
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73368128
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73368129
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73368131
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73368134
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73368138
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73368140
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73368143
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73368144
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73368146
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73368147
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs924859065
seq_region_name: 17
source: dbSNP
start: 73368149
strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73368154
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73368158
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73368176
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73368178
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145436598
seq_region_name: 17
source: dbSNP
start: 73368179
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs943487967
seq_region_name: 17
source: dbSNP
start: 73368182
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1469869437
seq_region_name: 17
source: dbSNP
start: 73368184
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062701649
seq_region_name: 17
source: dbSNP
start: 73368185
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1292747175
seq_region_name: 17
source: dbSNP
start: 73368186
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062701688
seq_region_name: 17
source: dbSNP
start: 73368190
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062701712
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062701735
seq_region_name: 17
source: dbSNP
start: 73368193
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062701763
seq_region_name: 17
source: dbSNP
start: 73368199
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs57025115
seq_region_name: 17
source: dbSNP
start: 73368200
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145436675
seq_region_name: 17
source: dbSNP
start: 73368202
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs901894683
seq_region_name: 17
source: dbSNP
start: 73368203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145436687
seq_region_name: 17
source: dbSNP
start: 73368204
strand: 1
-
alleles:
- ATGGGGA
- ATGGGGATGGGGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs933312941
seq_region_name: 17
source: dbSNP
start: 73368208
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1168387820
seq_region_name: 17
source: dbSNP
start: 73368209
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1465201743
seq_region_name: 17
source: dbSNP
start: 73368210
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs914258092
seq_region_name: 17
source: dbSNP
start: 73368211
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1424459855
seq_region_name: 17
source: dbSNP
start: 73368212
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062701938
seq_region_name: 17
source: dbSNP
start: 73368214
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1173032107
seq_region_name: 17
source: dbSNP
start: 73368221
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368222
feature_type: variation
id: rs2062701982
seq_region_name: 17
source: dbSNP
start: 73368222
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1464857093
seq_region_name: 17
source: dbSNP
start: 73368226
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062702006
seq_region_name: 17
source: dbSNP
start: 73368237
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368239
feature_type: variation
id: rs2062702032
seq_region_name: 17
source: dbSNP
start: 73368239
strand: 1
-
alleles:
- CTCC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1424817686
seq_region_name: 17
source: dbSNP
start: 73368241
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1047738318
seq_region_name: 17
source: dbSNP
start: 73368245
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062702094
seq_region_name: 17
source: dbSNP
start: 73368246
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062702111
seq_region_name: 17
source: dbSNP
start: 73368247
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs943266702
seq_region_name: 17
source: dbSNP
start: 73368252
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368253
feature_type: variation
id: rs1489747259
seq_region_name: 17
source: dbSNP
start: 73368253
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368254
feature_type: variation
id: rs1039368274
seq_region_name: 17
source: dbSNP
start: 73368254
strand: 1
-
alleles:
- TCTCT
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062702192
seq_region_name: 17
source: dbSNP
start: 73368259
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368262
feature_type: variation
id: rs1374665238
seq_region_name: 17
source: dbSNP
start: 73368262
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368263
feature_type: variation
id: rs2062702250
seq_region_name: 17
source: dbSNP
start: 73368263
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368267
feature_type: variation
id: rs1016533350
seq_region_name: 17
source: dbSNP
start: 73368267
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368270
feature_type: variation
id: rs2062702338
seq_region_name: 17
source: dbSNP
start: 73368270
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368273
feature_type: variation
id: rs2062702368
seq_region_name: 17
source: dbSNP
start: 73368273
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368274
feature_type: variation
id: rs2062702392
seq_region_name: 17
source: dbSNP
start: 73368274
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368275
feature_type: variation
id: rs894973582
seq_region_name: 17
source: dbSNP
start: 73368275
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368277
feature_type: variation
id: rs2062702426
seq_region_name: 17
source: dbSNP
start: 73368277
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368278
feature_type: variation
id: rs2062702466
seq_region_name: 17
source: dbSNP
start: 73368278
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368280
feature_type: variation
id: rs2270725
seq_region_name: 17
source: dbSNP
start: 73368280
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368281
feature_type: variation
id: rs997366551
seq_region_name: 17
source: dbSNP
start: 73368281
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368281
feature_type: variation
id: rs2062702617
seq_region_name: 17
source: dbSNP
start: 73368281
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368283
feature_type: variation
id: rs2062702666
seq_region_name: 17
source: dbSNP
start: 73368283
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368288
feature_type: variation
id: rs1369600810
seq_region_name: 17
source: dbSNP
start: 73368288
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368292
feature_type: variation
id: rs531286757
seq_region_name: 17
source: dbSNP
start: 73368292
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368295
feature_type: variation
id: rs2062702765
seq_region_name: 17
source: dbSNP
start: 73368295
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368296
feature_type: variation
id: rs138932660
seq_region_name: 17
source: dbSNP
start: 73368296
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368296
feature_type: variation
id: rs1445980062
seq_region_name: 17
source: dbSNP
start: 73368297
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368297
feature_type: variation
id: rs886503269
seq_region_name: 17
source: dbSNP
start: 73368297
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368301
feature_type: variation
id: rs2062702912
seq_region_name: 17
source: dbSNP
start: 73368301
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368302
feature_type: variation
id: rs1280991813
seq_region_name: 17
source: dbSNP
start: 73368302
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368303
feature_type: variation
id: rs2062702987
seq_region_name: 17
source: dbSNP
start: 73368303
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368305
feature_type: variation
id: rs1599490305
seq_region_name: 17
source: dbSNP
start: 73368305
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368309
feature_type: variation
id: rs1030637751
seq_region_name: 17
source: dbSNP
start: 73368309
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368312
feature_type: variation
id: rs2062703067
seq_region_name: 17
source: dbSNP
start: 73368312
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368313
feature_type: variation
id: rs2145436975
seq_region_name: 17
source: dbSNP
start: 73368313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368314
feature_type: variation
id: rs2062703106
seq_region_name: 17
source: dbSNP
start: 73368314
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368315
feature_type: variation
id: rs956513978
seq_region_name: 17
source: dbSNP
start: 73368315
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368317
feature_type: variation
id: rs2062703176
seq_region_name: 17
source: dbSNP
start: 73368317
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368322
feature_type: variation
id: rs1177214869
seq_region_name: 17
source: dbSNP
start: 73368322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368324
feature_type: variation
id: rs2062703251
seq_region_name: 17
source: dbSNP
start: 73368324
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368326
feature_type: variation
id: rs2062703288
seq_region_name: 17
source: dbSNP
start: 73368326
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368327
feature_type: variation
id: rs1599490326
seq_region_name: 17
source: dbSNP
start: 73368327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368332
feature_type: variation
id: rs866133886
seq_region_name: 17
source: dbSNP
start: 73368332
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368333
feature_type: variation
id: rs1251621642
seq_region_name: 17
source: dbSNP
start: 73368333
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368337
feature_type: variation
id: rs2062703398
seq_region_name: 17
source: dbSNP
start: 73368337
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368338
feature_type: variation
id: rs1178517897
seq_region_name: 17
source: dbSNP
start: 73368338
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368340
feature_type: variation
id: rs2062703465
seq_region_name: 17
source: dbSNP
start: 73368340
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368342
feature_type: variation
id: rs1440863055
seq_region_name: 17
source: dbSNP
start: 73368342
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368344
feature_type: variation
id: rs2145437069
seq_region_name: 17
source: dbSNP
start: 73368344
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368345
feature_type: variation
id: rs2062703539
seq_region_name: 17
source: dbSNP
start: 73368345
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368347
feature_type: variation
id: rs182180560
seq_region_name: 17
source: dbSNP
start: 73368347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368349
feature_type: variation
id: rs1200059995
seq_region_name: 17
source: dbSNP
start: 73368349
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368354
feature_type: variation
id: rs2062703654
seq_region_name: 17
source: dbSNP
start: 73368354
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368357
feature_type: variation
id: rs747046196
seq_region_name: 17
source: dbSNP
start: 73368357
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368358
feature_type: variation
id: rs768632941
seq_region_name: 17
source: dbSNP
start: 73368358
strand: 1
-
alleles:
- CCCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368363
feature_type: variation
id: rs1348385250
seq_region_name: 17
source: dbSNP
start: 73368358
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368359
feature_type: variation
id: rs776871358
seq_region_name: 17
source: dbSNP
start: 73368359
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368360
feature_type: variation
id: rs959642780
seq_region_name: 17
source: dbSNP
start: 73368360
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368361
feature_type: variation
id: rs1361301509
seq_region_name: 17
source: dbSNP
start: 73368361
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368363
feature_type: variation
id: rs373438261
seq_region_name: 17
source: dbSNP
start: 73368363
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368364
feature_type: variation
id: rs770189383
seq_region_name: 17
source: dbSNP
start: 73368364
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368366
feature_type: variation
id: rs1483210159
seq_region_name: 17
source: dbSNP
start: 73368366
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368368
feature_type: variation
id: rs1183272868
seq_region_name: 17
source: dbSNP
start: 73368368
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368369
feature_type: variation
id: rs773694599
seq_region_name: 17
source: dbSNP
start: 73368369
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368370
feature_type: variation
id: rs923369856
seq_region_name: 17
source: dbSNP
start: 73368370
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368371
feature_type: variation
id: rs1599490399
seq_region_name: 17
source: dbSNP
start: 73368371
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368372
feature_type: variation
id: rs1469014969
seq_region_name: 17
source: dbSNP
start: 73368372
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368373
feature_type: variation
id: rs763473550
seq_region_name: 17
source: dbSNP
start: 73368373
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368374
feature_type: variation
id: rs1386466474
seq_region_name: 17
source: dbSNP
start: 73368374
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368375
feature_type: variation
id: rs1426913876
seq_region_name: 17
source: dbSNP
start: 73368375
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368376
feature_type: variation
id: rs149250167
seq_region_name: 17
source: dbSNP
start: 73368376
strand: 1
-
alleles:
- CCCCTCCCCTCCTCAGGGCCCCCTC
- CCCCTCCCCTCCTCAGGGCCCCCTCCCCTCCTCAGGGCCCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73368400
feature_type: variation
id: rs2062704153
seq_region_name: 17
source: dbSNP
start: 73368376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368377
feature_type: variation
id: rs752017450
seq_region_name: 17
source: dbSNP
start: 73368377
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368378
feature_type: variation
id: rs1568368368
seq_region_name: 17
source: dbSNP
start: 73368378
strand: 1
-
alleles:
- CTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368381
feature_type: variation
id: rs2062704217
seq_region_name: 17
source: dbSNP
start: 73368379
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368381
feature_type: variation
id: rs933365478
seq_region_name: 17
source: dbSNP
start: 73368381
strand: 1
-
alleles:
- CCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368384
feature_type: variation
id: rs2062704265
seq_region_name: 17
source: dbSNP
start: 73368381
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368385
feature_type: variation
id: rs1330901506
seq_region_name: 17
source: dbSNP
start: 73368385
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368389
feature_type: variation
id: rs759041349
seq_region_name: 17
source: dbSNP
start: 73368389
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368390
feature_type: variation
id: rs1467796603
seq_region_name: 17
source: dbSNP
start: 73368390
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368391
feature_type: variation
id: rs766970530
seq_region_name: 17
source: dbSNP
start: 73368391
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368392
feature_type: variation
id: rs978217532
seq_region_name: 17
source: dbSNP
start: 73368392
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368393
feature_type: variation
id: rs752249041
seq_region_name: 17
source: dbSNP
start: 73368393
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368394
feature_type: variation
id: rs372457326
seq_region_name: 17
source: dbSNP
start: 73368394
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368395
feature_type: variation
id: rs955782708
seq_region_name: 17
source: dbSNP
start: 73368395
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368397
feature_type: variation
id: rs2062704452
seq_region_name: 17
source: dbSNP
start: 73368397
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73368399
feature_type: variation
id: rs747138943
seq_region_name: 17
source: dbSNP
start: 73368399
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73368401
feature_type: variation
id: rs2062704503
seq_region_name: 17
source: dbSNP
start: 73368401
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73368402
feature_type: variation
id: rs2062704522
seq_region_name: 17
source: dbSNP
start: 73368402
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73368403
feature_type: variation
id: rs886421269
seq_region_name: 17
source: dbSNP
start: 73368403
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73368404
feature_type: variation
id: rs777461767
seq_region_name: 17
source: dbSNP
start: 73368404
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73368405
feature_type: variation
id: rs1339575243
seq_region_name: 17
source: dbSNP
start: 73368405
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368417
feature_type: variation
id: rs990315661
seq_region_name: 17
source: dbSNP
start: 73368417
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368420
feature_type: variation
id: rs1254896317
seq_region_name: 17
source: dbSNP
start: 73368420
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368425
feature_type: variation
id: rs1270209758
seq_region_name: 17
source: dbSNP
start: 73368425
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368427
feature_type: variation
id: rs1436704993
seq_region_name: 17
source: dbSNP
start: 73368427
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73368431
feature_type: variation
id: rs1187693877
seq_region_name: 17
source: dbSNP
start: 73368431
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368431
feature_type: variation
id: rs1599490495
seq_region_name: 17
source: dbSNP
start: 73368431
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368432
feature_type: variation
id: rs914205310
seq_region_name: 17
source: dbSNP
start: 73368432
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368433
feature_type: variation
id: rs1447041628
seq_region_name: 17
source: dbSNP
start: 73368433
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368435
feature_type: variation
id: rs2145437412
seq_region_name: 17
source: dbSNP
start: 73368435
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368436
feature_type: variation
id: rs753625971
seq_region_name: 17
source: dbSNP
start: 73368436
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368437
feature_type: variation
id: rs1385013045
seq_region_name: 17
source: dbSNP
start: 73368437
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73368438
feature_type: variation
id: rs139535646
seq_region_name: 17
source: dbSNP
start: 73368438
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368440
feature_type: variation
id: rs2062704929
seq_region_name: 17
source: dbSNP
start: 73368440
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368442
feature_type: variation
id: rs772085587
seq_region_name: 17
source: dbSNP
start: 73368442
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368443
feature_type: variation
id: rs781109587
seq_region_name: 17
source: dbSNP
start: 73368443
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368445
feature_type: variation
id: rs1409448556
seq_region_name: 17
source: dbSNP
start: 73368445
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368449
feature_type: variation
id: rs1337535166
seq_region_name: 17
source: dbSNP
start: 73368449
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368452
feature_type: variation
id: rs748296026
seq_region_name: 17
source: dbSNP
start: 73368452
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368455
feature_type: variation
id: rs1450359014
seq_region_name: 17
source: dbSNP
start: 73368455
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368458
feature_type: variation
id: rs1314052840
seq_region_name: 17
source: dbSNP
start: 73368458
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368459
feature_type: variation
id: rs376479672
seq_region_name: 17
source: dbSNP
start: 73368459
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368460
feature_type: variation
id: rs1229405715
seq_region_name: 17
source: dbSNP
start: 73368460
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368461
feature_type: variation
id: rs773569528
seq_region_name: 17
source: dbSNP
start: 73368461
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368462
feature_type: variation
id: rs763350090
seq_region_name: 17
source: dbSNP
start: 73368462
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73368463
feature_type: variation
id: rs771220422
seq_region_name: 17
source: dbSNP
start: 73368463
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368465
feature_type: variation
id: rs923173499
seq_region_name: 17
source: dbSNP
start: 73368465
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368468
feature_type: variation
id: rs2062705349
seq_region_name: 17
source: dbSNP
start: 73368468
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73368470
feature_type: variation
id: rs774885043
seq_region_name: 17
source: dbSNP
start: 73368470
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368471
feature_type: variation
id: rs768123458
seq_region_name: 17
source: dbSNP
start: 73368471
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368474
feature_type: variation
id: rs752194038
seq_region_name: 17
source: dbSNP
start: 73368474
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368476
feature_type: variation
id: rs760245135
seq_region_name: 17
source: dbSNP
start: 73368476
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368477
feature_type: variation
id: rs763670503
seq_region_name: 17
source: dbSNP
start: 73368477
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368478
feature_type: variation
id: rs1397940898
seq_region_name: 17
source: dbSNP
start: 73368478
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73368485
feature_type: variation
id: rs774334957
seq_region_name: 17
source: dbSNP
start: 73368485
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368486
feature_type: variation
id: rs1475216025
seq_region_name: 17
source: dbSNP
start: 73368486
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368489
feature_type: variation
id: rs146100082
seq_region_name: 17
source: dbSNP
start: 73368489
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368490
feature_type: variation
id: rs778540581
seq_region_name: 17
source: dbSNP
start: 73368490
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368491
feature_type: variation
id: rs1468120322
seq_region_name: 17
source: dbSNP
start: 73368491
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368492
feature_type: variation
id: rs140121891
seq_region_name: 17
source: dbSNP
start: 73368492
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73368493
feature_type: variation
id: rs758255463
seq_region_name: 17
source: dbSNP
start: 73368493
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368495
feature_type: variation
id: rs1457851700
seq_region_name: 17
source: dbSNP
start: 73368495
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368497
feature_type: variation
id: rs2062705776
seq_region_name: 17
source: dbSNP
start: 73368497
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368508
feature_type: variation
id: rs761561326
seq_region_name: 17
source: dbSNP
start: 73368508
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73368516
feature_type: variation
id: rs1164941957
seq_region_name: 17
source: dbSNP
start: 73368516
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73368517
feature_type: variation
id: rs2062705856
seq_region_name: 17
source: dbSNP
start: 73368517
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1568368502
seq_region_name: 17
source: dbSNP
start: 73368519
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs748167512
seq_region_name: 17
source: dbSNP
start: 73368521
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
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feature_type: variation
id: rs778089846
seq_region_name: 17
source: dbSNP
start: 73368522
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
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feature_type: variation
id: rs143843586
seq_region_name: 17
source: dbSNP
start: 73368523
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1265094048
seq_region_name: 17
source: dbSNP
start: 73368527
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
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feature_type: variation
id: rs1284600293
seq_region_name: 17
source: dbSNP
start: 73368530
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1320833906
seq_region_name: 17
source: dbSNP
start: 73368533
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs774560755
seq_region_name: 17
source: dbSNP
start: 73368536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1255916188
seq_region_name: 17
source: dbSNP
start: 73368538
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1486511702
seq_region_name: 17
source: dbSNP
start: 73368541
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1207204015
seq_region_name: 17
source: dbSNP
start: 73368542
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs746305717
seq_region_name: 17
source: dbSNP
start: 73368543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs772454614
seq_region_name: 17
source: dbSNP
start: 73368544
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1200442656
seq_region_name: 17
source: dbSNP
start: 73368545
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2145437797
seq_region_name: 17
source: dbSNP
start: 73368547
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1431779011
seq_region_name: 17
source: dbSNP
start: 73368549
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1472088772
seq_region_name: 17
source: dbSNP
start: 73368552
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
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feature_type: variation
id: rs775980806
seq_region_name: 17
source: dbSNP
start: 73368553
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
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feature_type: variation
id: rs760122266
seq_region_name: 17
source: dbSNP
start: 73368554
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs2145437832
seq_region_name: 17
source: dbSNP
start: 73368558
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1277758724
seq_region_name: 17
source: dbSNP
start: 73368561
strand: 1
-
alleles:
- GAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
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feature_type: variation
id: rs1364302595
seq_region_name: 17
source: dbSNP
start: 73368561
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1382272633
seq_region_name: 17
source: dbSNP
start: 73368562
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1568368561
seq_region_name: 17
source: dbSNP
start: 73368563
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs370494633
seq_region_name: 17
source: dbSNP
start: 73368564
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2062706563
seq_region_name: 17
source: dbSNP
start: 73368565
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1457580350
seq_region_name: 17
source: dbSNP
start: 73368567
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1384013109
seq_region_name: 17
source: dbSNP
start: 73368568
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1405128630
seq_region_name: 17
source: dbSNP
start: 73368569
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs143426374
seq_region_name: 17
source: dbSNP
start: 73368571
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs201886541
seq_region_name: 17
source: dbSNP
start: 73368572
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs750179738
seq_region_name: 17
source: dbSNP
start: 73368576
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1307101450
seq_region_name: 17
source: dbSNP
start: 73368577
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2062706787
seq_region_name: 17
source: dbSNP
start: 73368581
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
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feature_type: variation
id: rs1317976920
seq_region_name: 17
source: dbSNP
start: 73368583
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1241841784
seq_region_name: 17
source: dbSNP
start: 73368589
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1031095260
seq_region_name: 17
source: dbSNP
start: 73368593
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs923423772
seq_region_name: 17
source: dbSNP
start: 73368597
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs1353405576
seq_region_name: 17
source: dbSNP
start: 73368598
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs758213361
seq_region_name: 17
source: dbSNP
start: 73368600
strand: 1
-
alleles:
- AGGATGTGGGAGTGAGG
- AGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs1459030544
seq_region_name: 17
source: dbSNP
start: 73368607
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368613
feature_type: variation
id: rs954801970
seq_region_name: 17
source: dbSNP
start: 73368613
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368614
feature_type: variation
id: rs376634726
seq_region_name: 17
source: dbSNP
start: 73368614
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368616
feature_type: variation
id: rs1477952171
seq_region_name: 17
source: dbSNP
start: 73368616
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062707077
seq_region_name: 17
source: dbSNP
start: 73368618
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368620
feature_type: variation
id: rs2062707099
seq_region_name: 17
source: dbSNP
start: 73368620
strand: 1
-
alleles:
- GGGGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368626
feature_type: variation
id: rs768860208
seq_region_name: 17
source: dbSNP
start: 73368622
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368624
feature_type: variation
id: rs2145438008
seq_region_name: 17
source: dbSNP
start: 73368624
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368625
feature_type: variation
id: rs1190632570
seq_region_name: 17
source: dbSNP
start: 73368625
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368626
feature_type: variation
id: rs371174284
seq_region_name: 17
source: dbSNP
start: 73368626
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368628
feature_type: variation
id: rs2062707204
seq_region_name: 17
source: dbSNP
start: 73368628
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368629
feature_type: variation
id: rs756219787
seq_region_name: 17
source: dbSNP
start: 73368629
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368629
feature_type: variation
id: rs776915711
seq_region_name: 17
source: dbSNP
start: 73368629
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368633
feature_type: variation
id: rs1211592443
seq_region_name: 17
source: dbSNP
start: 73368630
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368631
feature_type: variation
id: rs540452011
seq_region_name: 17
source: dbSNP
start: 73368631
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368632
feature_type: variation
id: rs1286841184
seq_region_name: 17
source: dbSNP
start: 73368632
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368633
feature_type: variation
id: rs375414527
seq_region_name: 17
source: dbSNP
start: 73368633
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368634
feature_type: variation
id: rs1568368631
seq_region_name: 17
source: dbSNP
start: 73368634
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368636
feature_type: variation
id: rs942048571
seq_region_name: 17
source: dbSNP
start: 73368636
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368637
feature_type: variation
id: rs2062707534
seq_region_name: 17
source: dbSNP
start: 73368637
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368638
feature_type: variation
id: rs1165300180
seq_region_name: 17
source: dbSNP
start: 73368638
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368639
feature_type: variation
id: rs1568368634
seq_region_name: 17
source: dbSNP
start: 73368639
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368640
feature_type: variation
id: rs1320354316
seq_region_name: 17
source: dbSNP
start: 73368640
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368641
feature_type: variation
id: rs2145438072
seq_region_name: 17
source: dbSNP
start: 73368641
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368642
feature_type: variation
id: rs1273428991
seq_region_name: 17
source: dbSNP
start: 73368642
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368646
feature_type: variation
id: rs796101816
seq_region_name: 17
source: dbSNP
start: 73368646
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368649
feature_type: variation
id: rs1038066557
seq_region_name: 17
source: dbSNP
start: 73368649
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368653
feature_type: variation
id: rs1326064503
seq_region_name: 17
source: dbSNP
start: 73368653
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368655
feature_type: variation
id: rs1445248045
seq_region_name: 17
source: dbSNP
start: 73368655
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368656
feature_type: variation
id: rs2062707765
seq_region_name: 17
source: dbSNP
start: 73368656
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368658
feature_type: variation
id: rs746789632
seq_region_name: 17
source: dbSNP
start: 73368658
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368663
feature_type: variation
id: rs1330101025
seq_region_name: 17
source: dbSNP
start: 73368663
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368667
feature_type: variation
id: rs2062707802
seq_region_name: 17
source: dbSNP
start: 73368667
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368673
feature_type: variation
id: rs2145438124
seq_region_name: 17
source: dbSNP
start: 73368673
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368677
feature_type: variation
id: rs1465816544
seq_region_name: 17
source: dbSNP
start: 73368677
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368678
feature_type: variation
id: rs916514344
seq_region_name: 17
source: dbSNP
start: 73368678
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368679
feature_type: variation
id: rs1170575797
seq_region_name: 17
source: dbSNP
start: 73368679
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368682
feature_type: variation
id: rs1477600281
seq_region_name: 17
source: dbSNP
start: 73368682
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368685
feature_type: variation
id: rs2062707909
seq_region_name: 17
source: dbSNP
start: 73368685
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368687
feature_type: variation
id: rs555551164
seq_region_name: 17
source: dbSNP
start: 73368687
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368688
feature_type: variation
id: rs923792849
seq_region_name: 17
source: dbSNP
start: 73368688
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368689
feature_type: variation
id: rs2062707974
seq_region_name: 17
source: dbSNP
start: 73368689
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368691
feature_type: variation
id: rs2062707997
seq_region_name: 17
source: dbSNP
start: 73368691
strand: 1
-
alleles:
- GAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73368695
feature_type: variation
id: rs2062708013
seq_region_name: 17
source: dbSNP
start: 73368693
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73368903
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alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73368988
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73368991
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369005
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369011
strand: 1
-
alleles:
- AAAAAAAAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs56761775
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369013
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369018
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369023
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369025
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369025
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369026
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369027
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369027
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369027
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369035
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369038
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369039
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369043
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369044
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1196303041
seq_region_name: 17
source: dbSNP
start: 73369046
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062712045
seq_region_name: 17
source: dbSNP
start: 73369047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1029966498
seq_region_name: 17
source: dbSNP
start: 73369048
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599491327
seq_region_name: 17
source: dbSNP
start: 73369049
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1278599483
seq_region_name: 17
source: dbSNP
start: 73369053
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062712149
seq_region_name: 17
source: dbSNP
start: 73369054
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1236201969
seq_region_name: 17
source: dbSNP
start: 73369057
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062712196
seq_region_name: 17
source: dbSNP
start: 73369058
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145438990
seq_region_name: 17
source: dbSNP
start: 73369060
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369061
feature_type: variation
id: rs754594038
seq_region_name: 17
source: dbSNP
start: 73369061
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062712247
seq_region_name: 17
source: dbSNP
start: 73369062
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73369070
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1039413414
seq_region_name: 17
source: dbSNP
start: 73369074
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs983343048
seq_region_name: 17
source: dbSNP
start: 73369080
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145439018
seq_region_name: 17
source: dbSNP
start: 73369081
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs907805159
seq_region_name: 17
source: dbSNP
start: 73369082
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs532382737
seq_region_name: 17
source: dbSNP
start: 73369084
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369086
feature_type: variation
id: rs1396718568
seq_region_name: 17
source: dbSNP
start: 73369086
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062712490
seq_region_name: 17
source: dbSNP
start: 73369089
strand: 1
-
alleles:
- CTCTGCCAGACA
- CTCTGCCAGACACTCTGCCAGACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369100
feature_type: variation
id: rs905752250
seq_region_name: 17
source: dbSNP
start: 73369089
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145439040
seq_region_name: 17
source: dbSNP
start: 73369094
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1030594493
seq_region_name: 17
source: dbSNP
start: 73369101
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369107
feature_type: variation
id: rs1401355457
seq_region_name: 17
source: dbSNP
start: 73369107
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369108
feature_type: variation
id: rs973625457
seq_region_name: 17
source: dbSNP
start: 73369108
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369113
feature_type: variation
id: rs1172965053
seq_region_name: 17
source: dbSNP
start: 73369113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369114
feature_type: variation
id: rs757410970
seq_region_name: 17
source: dbSNP
start: 73369114
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369116
feature_type: variation
id: rs552218954
seq_region_name: 17
source: dbSNP
start: 73369116
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369119
feature_type: variation
id: rs1423610396
seq_region_name: 17
source: dbSNP
start: 73369119
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369120
feature_type: variation
id: rs1424945430
seq_region_name: 17
source: dbSNP
start: 73369120
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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feature_type: variation
id: rs1298211075
seq_region_name: 17
source: dbSNP
start: 73369121
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1255881508
seq_region_name: 17
source: dbSNP
start: 73369125
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1374902999
seq_region_name: 17
source: dbSNP
start: 73369126
strand: 1
-
alleles:
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- A
- C
assembly_name: GRCh38
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feature_type: variation
id: rs1389224565
seq_region_name: 17
source: dbSNP
start: 73369126
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062712877
seq_region_name: 17
source: dbSNP
start: 73369129
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs748224763
seq_region_name: 17
source: dbSNP
start: 73369131
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs145969534
seq_region_name: 17
source: dbSNP
start: 73369132
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599491408
seq_region_name: 17
source: dbSNP
start: 73369137
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746152138
seq_region_name: 17
source: dbSNP
start: 73369138
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1294424850
seq_region_name: 17
source: dbSNP
start: 73369139
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369140
feature_type: variation
id: rs772440000
seq_region_name: 17
source: dbSNP
start: 73369140
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs370380723
seq_region_name: 17
source: dbSNP
start: 73369141
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369144
feature_type: variation
id: rs775927723
seq_region_name: 17
source: dbSNP
start: 73369144
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369145
feature_type: variation
id: rs747547179
seq_region_name: 17
source: dbSNP
start: 73369145
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369146
feature_type: variation
id: rs2062713107
seq_region_name: 17
source: dbSNP
start: 73369146
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369150
feature_type: variation
id: rs373082529
seq_region_name: 17
source: dbSNP
start: 73369150
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867999
seq_region_name: 17
source: dbSNP
start: 73369151
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs778224386
seq_region_name: 17
source: dbSNP
start: 73369156
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369160
feature_type: variation
id: rs1445177693
seq_region_name: 17
source: dbSNP
start: 73369160
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369162
feature_type: variation
id: rs141252111
seq_region_name: 17
source: dbSNP
start: 73369162
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs969368603
seq_region_name: 17
source: dbSNP
start: 73369163
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs761451577
seq_region_name: 17
source: dbSNP
start: 73369166
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369167
feature_type: variation
id: rs982040115
seq_region_name: 17
source: dbSNP
start: 73369167
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369168
feature_type: variation
id: rs1404338959
seq_region_name: 17
source: dbSNP
start: 73369168
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1170676104
seq_region_name: 17
source: dbSNP
start: 73369170
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369173
feature_type: variation
id: rs1355955551
seq_region_name: 17
source: dbSNP
start: 73369173
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369174
feature_type: variation
id: rs894033163
seq_region_name: 17
source: dbSNP
start: 73369174
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867998
seq_region_name: 17
source: dbSNP
start: 73369175
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1400138430
seq_region_name: 17
source: dbSNP
start: 73369177
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369179
feature_type: variation
id: rs1453994503
seq_region_name: 17
source: dbSNP
start: 73369179
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599491503
seq_region_name: 17
source: dbSNP
start: 73369181
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369182
feature_type: variation
id: rs2062713560
seq_region_name: 17
source: dbSNP
start: 73369182
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369185
feature_type: variation
id: rs141549202
seq_region_name: 17
source: dbSNP
start: 73369185
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369186
feature_type: variation
id: rs779431400
seq_region_name: 17
source: dbSNP
start: 73369186
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369189
feature_type: variation
id: rs2062713692
seq_region_name: 17
source: dbSNP
start: 73369189
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369191
feature_type: variation
id: rs1040266478
seq_region_name: 17
source: dbSNP
start: 73369191
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369197
feature_type: variation
id: rs1296526705
seq_region_name: 17
source: dbSNP
start: 73369197
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369199
feature_type: variation
id: rs1747359041
seq_region_name: 17
source: dbSNP
start: 73369199
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369200
feature_type: variation
id: rs1437118144
seq_region_name: 17
source: dbSNP
start: 73369200
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369214
feature_type: variation
id: rs2062713859
seq_region_name: 17
source: dbSNP
start: 73369214
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369215
feature_type: variation
id: rs75719526
seq_region_name: 17
source: dbSNP
start: 73369215
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369216
feature_type: variation
id: rs550774932
seq_region_name: 17
source: dbSNP
start: 73369216
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369218
feature_type: variation
id: rs1813247477
seq_region_name: 17
source: dbSNP
start: 73369218
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369222
feature_type: variation
id: rs995885517
seq_region_name: 17
source: dbSNP
start: 73369222
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369223
feature_type: variation
id: rs569267764
seq_region_name: 17
source: dbSNP
start: 73369223
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369224
feature_type: variation
id: rs954331498
seq_region_name: 17
source: dbSNP
start: 73369224
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369226
feature_type: variation
id: rs1178503937
seq_region_name: 17
source: dbSNP
start: 73369226
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369234
feature_type: variation
id: rs2062714037
seq_region_name: 17
source: dbSNP
start: 73369234
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369239
feature_type: variation
id: rs2062714061
seq_region_name: 17
source: dbSNP
start: 73369239
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369243
feature_type: variation
id: rs2062714080
seq_region_name: 17
source: dbSNP
start: 73369243
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369246
feature_type: variation
id: rs1482107119
seq_region_name: 17
source: dbSNP
start: 73369246
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369248
feature_type: variation
id: rs2062714123
seq_region_name: 17
source: dbSNP
start: 73369248
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369251
feature_type: variation
id: rs1004537885
seq_region_name: 17
source: dbSNP
start: 73369251
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369253
feature_type: variation
id: rs539854776
seq_region_name: 17
source: dbSNP
start: 73369253
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369257
feature_type: variation
id: rs1349942632
seq_region_name: 17
source: dbSNP
start: 73369257
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369262
feature_type: variation
id: rs1283739898
seq_region_name: 17
source: dbSNP
start: 73369262
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369264
feature_type: variation
id: rs1239377811
seq_region_name: 17
source: dbSNP
start: 73369264
strand: 1
-
alleles:
- CAGACAGA
- CAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369271
feature_type: variation
id: rs1378400453
seq_region_name: 17
source: dbSNP
start: 73369264
strand: 1
-
alleles:
- CAGACAGAGTGTGGTGCAAGTGCTGGTGGCCTCATGTCACCTGGGAGCTGGTG
- CAGACAGAGTGTGGTGCAAGTGCTGGTGGCCTCATGTCACCTGGGAGCTGGTGCAGACAGAGTGTGGTGCAAGTGCTGGTGGCCTCATGTCACCTGGGAGCTGGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369316
feature_type: variation
id: rs2062714273
seq_region_name: 17
source: dbSNP
start: 73369264
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369265
feature_type: variation
id: rs2145439393
seq_region_name: 17
source: dbSNP
start: 73369265
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369266
feature_type: variation
id: rs2062714302
seq_region_name: 17
source: dbSNP
start: 73369266
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369269
feature_type: variation
id: rs1354418234
seq_region_name: 17
source: dbSNP
start: 73369269
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369270
feature_type: variation
id: rs2062714350
seq_region_name: 17
source: dbSNP
start: 73369270
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369275
feature_type: variation
id: rs77984954
seq_region_name: 17
source: dbSNP
start: 73369275
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369279
feature_type: variation
id: rs1568368925
seq_region_name: 17
source: dbSNP
start: 73369279
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369280
feature_type: variation
id: rs2062714491
seq_region_name: 17
source: dbSNP
start: 73369280
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369284
feature_type: variation
id: rs2145439429
seq_region_name: 17
source: dbSNP
start: 73369284
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369285
feature_type: variation
id: rs2062714513
seq_region_name: 17
source: dbSNP
start: 73369285
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369288
feature_type: variation
id: rs1394494976
seq_region_name: 17
source: dbSNP
start: 73369288
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369297
feature_type: variation
id: rs2062714555
seq_region_name: 17
source: dbSNP
start: 73369297
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369298
feature_type: variation
id: rs1954553711
seq_region_name: 17
source: dbSNP
start: 73369298
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369306
feature_type: variation
id: rs1378803201
seq_region_name: 17
source: dbSNP
start: 73369306
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369307
feature_type: variation
id: rs1303758427
seq_region_name: 17
source: dbSNP
start: 73369307
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369308
feature_type: variation
id: rs899547638
seq_region_name: 17
source: dbSNP
start: 73369308
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369309
feature_type: variation
id: rs933644989
seq_region_name: 17
source: dbSNP
start: 73369309
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369312
feature_type: variation
id: rs1359048121
seq_region_name: 17
source: dbSNP
start: 73369312
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369319
feature_type: variation
id: rs2062714699
seq_region_name: 17
source: dbSNP
start: 73369319
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369320
feature_type: variation
id: rs2062714726
seq_region_name: 17
source: dbSNP
start: 73369320
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369322
feature_type: variation
id: rs868000
seq_region_name: 17
source: dbSNP
start: 73369322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369324
feature_type: variation
id: rs916361559
seq_region_name: 17
source: dbSNP
start: 73369324
strand: 1
-
alleles:
- AGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369328
feature_type: variation
id: rs2062714830
seq_region_name: 17
source: dbSNP
start: 73369325
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369326
feature_type: variation
id: rs969213448
seq_region_name: 17
source: dbSNP
start: 73369326
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369327
feature_type: variation
id: rs890725572
seq_region_name: 17
source: dbSNP
start: 73369327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369337
feature_type: variation
id: rs2062714901
seq_region_name: 17
source: dbSNP
start: 73369337
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369339
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73369454
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73369470
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369471
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73369478
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73369481
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369482
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73369483
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369484
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369489
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369490
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369492
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369500
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369501
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369504
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369510
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369511
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369512
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062716975
seq_region_name: 17
source: dbSNP
start: 73369515
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369521
feature_type: variation
id: rs2062716992
seq_region_name: 17
source: dbSNP
start: 73369521
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1196637770
seq_region_name: 17
source: dbSNP
start: 73369525
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062717034
seq_region_name: 17
source: dbSNP
start: 73369526
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369527
feature_type: variation
id: rs776624040
seq_region_name: 17
source: dbSNP
start: 73369527
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs373589207
seq_region_name: 17
source: dbSNP
start: 73369528
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369530
feature_type: variation
id: rs2062717082
seq_region_name: 17
source: dbSNP
start: 73369530
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369532
feature_type: variation
id: rs1023730837
seq_region_name: 17
source: dbSNP
start: 73369532
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369538
feature_type: variation
id: rs905316023
seq_region_name: 17
source: dbSNP
start: 73369538
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369540
feature_type: variation
id: rs1003567279
seq_region_name: 17
source: dbSNP
start: 73369540
strand: 1
-
alleles:
- C
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-
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-
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369619
strand: 1
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alleles:
- A
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73369628
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73369636
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369637
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599491988
seq_region_name: 17
source: dbSNP
start: 73369639
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73369641
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369642
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369648
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369649
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369653
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369657
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062718189
seq_region_name: 17
source: dbSNP
start: 73369658
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599492003
seq_region_name: 17
source: dbSNP
start: 73369660
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369661
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599492010
seq_region_name: 17
source: dbSNP
start: 73369664
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369664
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369667
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73369671
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs551806342
seq_region_name: 17
source: dbSNP
start: 73369679
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062718403
seq_region_name: 17
source: dbSNP
start: 73369681
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062718426
seq_region_name: 17
source: dbSNP
start: 73369682
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs367689086
seq_region_name: 17
source: dbSNP
start: 73369683
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs193163719
seq_region_name: 17
source: dbSNP
start: 73369684
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73369687
feature_type: variation
id: rs986545179
seq_region_name: 17
source: dbSNP
start: 73369687
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs571950237
seq_region_name: 17
source: dbSNP
start: 73369689
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369699
feature_type: variation
id: rs1455930361
seq_region_name: 17
source: dbSNP
start: 73369689
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs566871238
seq_region_name: 17
source: dbSNP
start: 73369690
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs866809278
seq_region_name: 17
source: dbSNP
start: 73369695
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369698
feature_type: variation
id: rs1599492061
seq_region_name: 17
source: dbSNP
start: 73369698
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369699
feature_type: variation
id: rs2145440415
seq_region_name: 17
source: dbSNP
start: 73369699
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369700
feature_type: variation
id: rs939684948
seq_region_name: 17
source: dbSNP
start: 73369700
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369701
feature_type: variation
id: rs1318127268
seq_region_name: 17
source: dbSNP
start: 73369701
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369703
feature_type: variation
id: rs1363396281
seq_region_name: 17
source: dbSNP
start: 73369703
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369704
feature_type: variation
id: rs2062718734
seq_region_name: 17
source: dbSNP
start: 73369704
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369707
feature_type: variation
id: rs2062718763
seq_region_name: 17
source: dbSNP
start: 73369707
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369711
feature_type: variation
id: rs1599492077
seq_region_name: 17
source: dbSNP
start: 73369711
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369712
feature_type: variation
id: rs2062718815
seq_region_name: 17
source: dbSNP
start: 73369712
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369713
feature_type: variation
id: rs887308169
seq_region_name: 17
source: dbSNP
start: 73369713
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369716
feature_type: variation
id: rs538906607
seq_region_name: 17
source: dbSNP
start: 73369716
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369717
feature_type: variation
id: rs1282933161
seq_region_name: 17
source: dbSNP
start: 73369717
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369719
feature_type: variation
id: rs1599492094
seq_region_name: 17
source: dbSNP
start: 73369719
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369721
feature_type: variation
id: rs920858422
seq_region_name: 17
source: dbSNP
start: 73369721
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369722
feature_type: variation
id: rs940383379
seq_region_name: 17
source: dbSNP
start: 73369722
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369724
feature_type: variation
id: rs2145440498
seq_region_name: 17
source: dbSNP
start: 73369724
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73369727
feature_type: variation
id: rs2145440508
seq_region_name: 17
source: dbSNP
start: 73369727
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73369924
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369925
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73369926
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73370098
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73370099
strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73370104
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73370107
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370108
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370119
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370119
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370121
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370122
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370130
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370131
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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end: 73370133
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370133
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370136
feature_type: variation
id: rs1233377341
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs766235948
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370165
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062722889
seq_region_name: 17
source: dbSNP
start: 73370168
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062722944
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs994302024
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1371135623
seq_region_name: 17
source: dbSNP
start: 73370185
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1192306026
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1275222285
seq_region_name: 17
source: dbSNP
start: 73370193
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1484021078
seq_region_name: 17
source: dbSNP
start: 73370198
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs992766311
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs914057231
seq_region_name: 17
source: dbSNP
start: 73370206
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723130
seq_region_name: 17
source: dbSNP
start: 73370211
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1468183996
seq_region_name: 17
source: dbSNP
start: 73370213
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568369263
seq_region_name: 17
source: dbSNP
start: 73370221
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723193
seq_region_name: 17
source: dbSNP
start: 73370224
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062723214
seq_region_name: 17
source: dbSNP
start: 73370228
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1273989738
seq_region_name: 17
source: dbSNP
start: 73370231
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1215820277
seq_region_name: 17
source: dbSNP
start: 73370232
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370234
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145441677
seq_region_name: 17
source: dbSNP
start: 73370237
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723321
seq_region_name: 17
source: dbSNP
start: 73370240
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723373
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370246
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723426
seq_region_name: 17
source: dbSNP
start: 73370251
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- TTTATTT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs945493131
seq_region_name: 17
source: dbSNP
start: 73370255
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723508
seq_region_name: 17
source: dbSNP
start: 73370264
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1228790957
seq_region_name: 17
source: dbSNP
start: 73370265
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1488526431
seq_region_name: 17
source: dbSNP
start: 73370267
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs147689088
seq_region_name: 17
source: dbSNP
start: 73370270
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1438019596
seq_region_name: 17
source: dbSNP
start: 73370273
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1422698695
seq_region_name: 17
source: dbSNP
start: 73370275
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062723628
seq_region_name: 17
source: dbSNP
start: 73370276
strand: 1
-
alleles:
- TGTT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs903905917
seq_region_name: 17
source: dbSNP
start: 73370278
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2097557821
seq_region_name: 17
source: dbSNP
start: 73370283
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs892366777
seq_region_name: 17
source: dbSNP
start: 73370288
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370289
feature_type: variation
id: rs2062723694
seq_region_name: 17
source: dbSNP
start: 73370289
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370291
feature_type: variation
id: rs932658089
seq_region_name: 17
source: dbSNP
start: 73370291
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062723745
seq_region_name: 17
source: dbSNP
start: 73370294
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1167178031
seq_region_name: 17
source: dbSNP
start: 73370298
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1173451071
seq_region_name: 17
source: dbSNP
start: 73370300
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062723783
seq_region_name: 17
source: dbSNP
start: 73370301
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062723810
seq_region_name: 17
source: dbSNP
start: 73370303
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370304
feature_type: variation
id: rs1009940054
seq_region_name: 17
source: dbSNP
start: 73370304
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370305
feature_type: variation
id: rs1043559570
seq_region_name: 17
source: dbSNP
start: 73370305
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370306
feature_type: variation
id: rs748010885
seq_region_name: 17
source: dbSNP
start: 73370306
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370307
feature_type: variation
id: rs2062723905
seq_region_name: 17
source: dbSNP
start: 73370307
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370309
feature_type: variation
id: rs2062723935
seq_region_name: 17
source: dbSNP
start: 73370309
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370310
feature_type: variation
id: rs1453826197
seq_region_name: 17
source: dbSNP
start: 73370310
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370311
feature_type: variation
id: rs2062723980
seq_region_name: 17
source: dbSNP
start: 73370311
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370321
feature_type: variation
id: rs1599492732
seq_region_name: 17
source: dbSNP
start: 73370321
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370322
feature_type: variation
id: rs1253707072
seq_region_name: 17
source: dbSNP
start: 73370322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370324
feature_type: variation
id: rs2062724056
seq_region_name: 17
source: dbSNP
start: 73370324
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370326
feature_type: variation
id: rs2062724080
seq_region_name: 17
source: dbSNP
start: 73370326
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370327
feature_type: variation
id: rs1195720156
seq_region_name: 17
source: dbSNP
start: 73370327
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370329
feature_type: variation
id: rs2062724125
seq_region_name: 17
source: dbSNP
start: 73370329
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370330
feature_type: variation
id: rs1436359233
seq_region_name: 17
source: dbSNP
start: 73370330
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370334
feature_type: variation
id: rs2062724168
seq_region_name: 17
source: dbSNP
start: 73370334
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370335
feature_type: variation
id: rs2062724190
seq_region_name: 17
source: dbSNP
start: 73370335
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370338
feature_type: variation
id: rs996901856
seq_region_name: 17
source: dbSNP
start: 73370338
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370341
feature_type: variation
id: rs1008127188
seq_region_name: 17
source: dbSNP
start: 73370341
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370345
feature_type: variation
id: rs1028424342
seq_region_name: 17
source: dbSNP
start: 73370345
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370347
feature_type: variation
id: rs955469793
seq_region_name: 17
source: dbSNP
start: 73370347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370349
feature_type: variation
id: rs2062724297
seq_region_name: 17
source: dbSNP
start: 73370349
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370353
feature_type: variation
id: rs1278766620
seq_region_name: 17
source: dbSNP
start: 73370353
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370355
feature_type: variation
id: rs2062724343
seq_region_name: 17
source: dbSNP
start: 73370355
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370356
feature_type: variation
id: rs2062724362
seq_region_name: 17
source: dbSNP
start: 73370356
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370357
feature_type: variation
id: rs1234209991
seq_region_name: 17
source: dbSNP
start: 73370357
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370364
feature_type: variation
id: rs1437353024
seq_region_name: 17
source: dbSNP
start: 73370364
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370372
feature_type: variation
id: rs1303578681
seq_region_name: 17
source: dbSNP
start: 73370372
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370378
feature_type: variation
id: rs183580267
seq_region_name: 17
source: dbSNP
start: 73370378
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370380
feature_type: variation
id: rs1234953567
seq_region_name: 17
source: dbSNP
start: 73370380
strand: 1
-
alleles:
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599492802
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source: dbSNP
start: 73370393
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370399
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1333661801
seq_region_name: 17
source: dbSNP
start: 73370401
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062724625
seq_region_name: 17
source: dbSNP
start: 73370403
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1391704837
seq_region_name: 17
source: dbSNP
start: 73370408
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599492837
seq_region_name: 17
source: dbSNP
start: 73370410
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs531594863
seq_region_name: 17
source: dbSNP
start: 73370415
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062724711
seq_region_name: 17
source: dbSNP
start: 73370418
strand: 1
-
alleles:
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- TTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1372208579
seq_region_name: 17
source: dbSNP
start: 73370418
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs961639800
seq_region_name: 17
source: dbSNP
start: 73370419
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145442070
seq_region_name: 17
source: dbSNP
start: 73370426
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1369098069
seq_region_name: 17
source: dbSNP
start: 73370431
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs995712044
seq_region_name: 17
source: dbSNP
start: 73370432
strand: 1
-
alleles:
- GGGG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1434038747
seq_region_name: 17
source: dbSNP
start: 73370432
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370433
feature_type: variation
id: rs2062724846
seq_region_name: 17
source: dbSNP
start: 73370433
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370435
feature_type: variation
id: rs2062724870
seq_region_name: 17
source: dbSNP
start: 73370435
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062724890
seq_region_name: 17
source: dbSNP
start: 73370440
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs772059138
seq_region_name: 17
source: dbSNP
start: 73370443
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1363394665
seq_region_name: 17
source: dbSNP
start: 73370445
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1026691461
seq_region_name: 17
source: dbSNP
start: 73370454
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062724982
seq_region_name: 17
source: dbSNP
start: 73370457
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs974735778
seq_region_name: 17
source: dbSNP
start: 73370458
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370459
feature_type: variation
id: rs2062725031
seq_region_name: 17
source: dbSNP
start: 73370459
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370463
feature_type: variation
id: rs1439855974
seq_region_name: 17
source: dbSNP
start: 73370463
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062725062
seq_region_name: 17
source: dbSNP
start: 73370467
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1297995780
seq_region_name: 17
source: dbSNP
start: 73370468
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599492888
seq_region_name: 17
source: dbSNP
start: 73370470
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs188215827
seq_region_name: 17
source: dbSNP
start: 73370475
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746814928
seq_region_name: 17
source: dbSNP
start: 73370478
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062725175
seq_region_name: 17
source: dbSNP
start: 73370479
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1272223271
seq_region_name: 17
source: dbSNP
start: 73370480
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1035307224
seq_region_name: 17
source: dbSNP
start: 73370481
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062725242
seq_region_name: 17
source: dbSNP
start: 73370488
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370489
feature_type: variation
id: rs2062725263
seq_region_name: 17
source: dbSNP
start: 73370489
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370490
feature_type: variation
id: rs2062725288
seq_region_name: 17
source: dbSNP
start: 73370490
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs961273940
seq_region_name: 17
source: dbSNP
start: 73370492
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370497
feature_type: variation
id: rs980462451
seq_region_name: 17
source: dbSNP
start: 73370497
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370500
feature_type: variation
id: rs914091956
seq_region_name: 17
source: dbSNP
start: 73370500
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1321784490
seq_region_name: 17
source: dbSNP
start: 73370502
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370503
feature_type: variation
id: rs926363120
seq_region_name: 17
source: dbSNP
start: 73370503
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370509
feature_type: variation
id: rs945573740
seq_region_name: 17
source: dbSNP
start: 73370509
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370518
feature_type: variation
id: rs1336117202
seq_region_name: 17
source: dbSNP
start: 73370518
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370521
feature_type: variation
id: rs979557133
seq_region_name: 17
source: dbSNP
start: 73370521
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370525
feature_type: variation
id: rs1223220567
seq_region_name: 17
source: dbSNP
start: 73370525
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370526
feature_type: variation
id: rs2062725495
seq_region_name: 17
source: dbSNP
start: 73370526
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370529
feature_type: variation
id: rs925371869
seq_region_name: 17
source: dbSNP
start: 73370529
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370531
feature_type: variation
id: rs2062725534
seq_region_name: 17
source: dbSNP
start: 73370531
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370537
feature_type: variation
id: rs2062725557
seq_region_name: 17
source: dbSNP
start: 73370537
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370538
feature_type: variation
id: rs939129169
seq_region_name: 17
source: dbSNP
start: 73370538
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370539
feature_type: variation
id: rs932709041
seq_region_name: 17
source: dbSNP
start: 73370539
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370543
feature_type: variation
id: rs2145442298
seq_region_name: 17
source: dbSNP
start: 73370543
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370544
feature_type: variation
id: rs1248993507
seq_region_name: 17
source: dbSNP
start: 73370544
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370546
feature_type: variation
id: rs1260162595
seq_region_name: 17
source: dbSNP
start: 73370546
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370550
feature_type: variation
id: rs1191705435
seq_region_name: 17
source: dbSNP
start: 73370550
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370551
feature_type: variation
id: rs1056055651
seq_region_name: 17
source: dbSNP
start: 73370551
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370552
feature_type: variation
id: rs2062725717
seq_region_name: 17
source: dbSNP
start: 73370552
strand: 1
-
alleles:
- ATTTTATTTTATTTTATTTTATTT
- ATTTTATTTTATTT
- ATTTTATTTTATTTTATTT
- ATTTTATTTTATTTTATTTTATTTTATTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370575
feature_type: variation
id: rs112485065
seq_region_name: 17
source: dbSNP
start: 73370552
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370553
feature_type: variation
id: rs2062725782
seq_region_name: 17
source: dbSNP
start: 73370553
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370556
feature_type: variation
id: rs1599493003
seq_region_name: 17
source: dbSNP
start: 73370556
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370557
feature_type: variation
id: rs1271016799
seq_region_name: 17
source: dbSNP
start: 73370557
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370558
feature_type: variation
id: rs2062725843
seq_region_name: 17
source: dbSNP
start: 73370558
strand: 1
-
alleles:
- TAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370563
feature_type: variation
id: rs1232401618
seq_region_name: 17
source: dbSNP
start: 73370561
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370571
feature_type: variation
id: rs199919210
seq_region_name: 17
source: dbSNP
start: 73370571
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370576
feature_type: variation
id: rs1355888521
seq_region_name: 17
source: dbSNP
start: 73370576
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370578
feature_type: variation
id: rs1451733594
seq_region_name: 17
source: dbSNP
start: 73370578
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370585
feature_type: variation
id: rs2062725967
seq_region_name: 17
source: dbSNP
start: 73370585
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370586
feature_type: variation
id: rs2062725993
seq_region_name: 17
source: dbSNP
start: 73370586
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370587
feature_type: variation
id: rs1285818113
seq_region_name: 17
source: dbSNP
start: 73370587
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370591
feature_type: variation
id: rs2145442403
seq_region_name: 17
source: dbSNP
start: 73370591
strand: 1
-
alleles:
- TTTT
- TTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370594
feature_type: variation
id: rs2062726033
seq_region_name: 17
source: dbSNP
start: 73370591
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370592
feature_type: variation
id: rs2062726058
seq_region_name: 17
source: dbSNP
start: 73370592
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370594
feature_type: variation
id: rs2062726072
seq_region_name: 17
source: dbSNP
start: 73370594
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370596
feature_type: variation
id: rs2062726098
seq_region_name: 17
source: dbSNP
start: 73370596
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370597
feature_type: variation
id: rs1036956742
seq_region_name: 17
source: dbSNP
start: 73370597
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370599
feature_type: variation
id: rs1325920237
seq_region_name: 17
source: dbSNP
start: 73370599
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370600
feature_type: variation
id: rs1419509800
seq_region_name: 17
source: dbSNP
start: 73370600
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370605
feature_type: variation
id: rs2062726194
seq_region_name: 17
source: dbSNP
start: 73370605
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370606
feature_type: variation
id: rs2062726220
seq_region_name: 17
source: dbSNP
start: 73370606
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370607
feature_type: variation
id: rs1458987004
seq_region_name: 17
source: dbSNP
start: 73370607
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370608
feature_type: variation
id: rs1392611395
seq_region_name: 17
source: dbSNP
start: 73370608
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370610
feature_type: variation
id: rs2062726269
seq_region_name: 17
source: dbSNP
start: 73370610
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370611
feature_type: variation
id: rs2062726290
seq_region_name: 17
source: dbSNP
start: 73370611
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73370795
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73370807
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370814
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73370819
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370819
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73370892
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370918
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370919
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370923
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370925
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370927
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370929
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73370934
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370936
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370937
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73370944
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370953
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370954
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370955
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370958
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1256672110
seq_region_name: 17
source: dbSNP
start: 73370959
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370961
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73370962
feature_type: variation
id: rs1450083177
seq_region_name: 17
source: dbSNP
start: 73370962
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370971
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370973
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370974
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370975
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370978
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1291370800
seq_region_name: 17
source: dbSNP
start: 73370985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1215330903
seq_region_name: 17
source: dbSNP
start: 73370987
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs542665185
seq_region_name: 17
source: dbSNP
start: 73370988
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs181815294
seq_region_name: 17
source: dbSNP
start: 73370989
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371006
feature_type: variation
id: rs2062730594
seq_region_name: 17
source: dbSNP
start: 73370989
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1020357615
seq_region_name: 17
source: dbSNP
start: 73370991
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370992
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062730651
seq_region_name: 17
source: dbSNP
start: 73370993
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370995
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370996
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73370999
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062730763
seq_region_name: 17
source: dbSNP
start: 73371000
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371001
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs967009492
seq_region_name: 17
source: dbSNP
start: 73371002
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062730917
seq_region_name: 17
source: dbSNP
start: 73371004
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371005
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371013
feature_type: variation
id: rs764653194
seq_region_name: 17
source: dbSNP
start: 73371013
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371018
feature_type: variation
id: rs2145443410
seq_region_name: 17
source: dbSNP
start: 73371018
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371019
feature_type: variation
id: rs2145443417
seq_region_name: 17
source: dbSNP
start: 73371019
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371023
feature_type: variation
id: rs2062731014
seq_region_name: 17
source: dbSNP
start: 73371023
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371031
feature_type: variation
id: rs1380689061
seq_region_name: 17
source: dbSNP
start: 73371031
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371033
feature_type: variation
id: rs1204205332
seq_region_name: 17
source: dbSNP
start: 73371033
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371038
feature_type: variation
id: rs954200992
seq_region_name: 17
source: dbSNP
start: 73371038
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371041
feature_type: variation
id: rs2062731098
seq_region_name: 17
source: dbSNP
start: 73371041
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371046
feature_type: variation
id: rs1283950672
seq_region_name: 17
source: dbSNP
start: 73371046
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371049
feature_type: variation
id: rs2145443462
seq_region_name: 17
source: dbSNP
start: 73371049
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371052
feature_type: variation
id: rs2062731144
seq_region_name: 17
source: dbSNP
start: 73371052
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371057
feature_type: variation
id: rs2145443481
seq_region_name: 17
source: dbSNP
start: 73371057
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371059
feature_type: variation
id: rs1443355703
seq_region_name: 17
source: dbSNP
start: 73371059
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371088
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73371096
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1414444625
seq_region_name: 17
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start: 73371099
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
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feature_type: variation
id: rs2062731650
seq_region_name: 17
source: dbSNP
start: 73371102
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371104
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371105
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1433646320
seq_region_name: 17
source: dbSNP
start: 73371109
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371113
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145443725
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source: dbSNP
start: 73371114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371118
strand: 1
-
alleles:
- GGCAGT
- GGCAGTGGCAGT
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371127
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371135
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371139
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371142
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371149
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371155
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371159
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371162
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371163
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371173
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1661608135
seq_region_name: 17
source: dbSNP
start: 73371174
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371178
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371180
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371184
feature_type: variation
id: rs7221596
seq_region_name: 17
source: dbSNP
start: 73371184
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371191
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1048293440
seq_region_name: 17
source: dbSNP
start: 73371195
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73371201
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371201
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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end: 73371212
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371212
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371214
feature_type: variation
id: rs927180281
seq_region_name: 17
source: dbSNP
start: 73371214
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371216
feature_type: variation
id: rs937179619
seq_region_name: 17
source: dbSNP
start: 73371216
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062732279
seq_region_name: 17
source: dbSNP
start: 73371218
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371220
feature_type: variation
id: rs2062732308
seq_region_name: 17
source: dbSNP
start: 73371220
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1057344560
seq_region_name: 17
source: dbSNP
start: 73371223
strand: 1
-
alleles:
- TGATGCTAAAAGTTTGCCATTATTAGCACACAGGTGGTCTTCCGTGA
- TGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371270
feature_type: variation
id: rs367694529
seq_region_name: 17
source: dbSNP
start: 73371224
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371225
feature_type: variation
id: rs1374815327
seq_region_name: 17
source: dbSNP
start: 73371225
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371226
feature_type: variation
id: rs1212054793
seq_region_name: 17
source: dbSNP
start: 73371226
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371233
feature_type: variation
id: rs565909206
seq_region_name: 17
source: dbSNP
start: 73371233
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371237
feature_type: variation
id: rs2145443960
seq_region_name: 17
source: dbSNP
start: 73371237
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371240
feature_type: variation
id: rs2062732433
seq_region_name: 17
source: dbSNP
start: 73371240
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371243
feature_type: variation
id: rs2062732457
seq_region_name: 17
source: dbSNP
start: 73371243
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371245
feature_type: variation
id: rs2062732477
seq_region_name: 17
source: dbSNP
start: 73371245
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371247
feature_type: variation
id: rs1479874726
seq_region_name: 17
source: dbSNP
start: 73371247
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371258
feature_type: variation
id: rs1251180544
seq_region_name: 17
source: dbSNP
start: 73371258
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371262
feature_type: variation
id: rs2062732539
seq_region_name: 17
source: dbSNP
start: 73371262
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371266
feature_type: variation
id: rs2062732556
seq_region_name: 17
source: dbSNP
start: 73371266
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371267
feature_type: variation
id: rs1037538950
seq_region_name: 17
source: dbSNP
start: 73371267
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371271
feature_type: variation
id: rs762211392
seq_region_name: 17
source: dbSNP
start: 73371271
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371272
feature_type: variation
id: rs1333506109
seq_region_name: 17
source: dbSNP
start: 73371272
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371273
feature_type: variation
id: rs2062732653
seq_region_name: 17
source: dbSNP
start: 73371273
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371276
feature_type: variation
id: rs2062732670
seq_region_name: 17
source: dbSNP
start: 73371276
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371280
feature_type: variation
id: rs2145444057
seq_region_name: 17
source: dbSNP
start: 73371280
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371286
feature_type: variation
id: rs1231592019
seq_region_name: 17
source: dbSNP
start: 73371286
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371287
feature_type: variation
id: rs1330206502
seq_region_name: 17
source: dbSNP
start: 73371287
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371289
feature_type: variation
id: rs945768696
seq_region_name: 17
source: dbSNP
start: 73371289
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371291
feature_type: variation
id: rs565438149
seq_region_name: 17
source: dbSNP
start: 73371291
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371292
feature_type: variation
id: rs2062732781
seq_region_name: 17
source: dbSNP
start: 73371292
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371293
feature_type: variation
id: rs2062732805
seq_region_name: 17
source: dbSNP
start: 73371293
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371299
feature_type: variation
id: rs2062732833
seq_region_name: 17
source: dbSNP
start: 73371299
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371301
feature_type: variation
id: rs757661738
seq_region_name: 17
source: dbSNP
start: 73371301
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371304
feature_type: variation
id: rs1394071719
seq_region_name: 17
source: dbSNP
start: 73371304
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371305
feature_type: variation
id: rs2062732915
seq_region_name: 17
source: dbSNP
start: 73371305
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371308
feature_type: variation
id: rs536301959
seq_region_name: 17
source: dbSNP
start: 73371308
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371312
feature_type: variation
id: rs2062732961
seq_region_name: 17
source: dbSNP
start: 73371312
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371317
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73371530
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73371542
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73371552
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73371555
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73371556
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73371557
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371560
strand: 1
-
alleles:
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- AGA
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73371568
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371569
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371575
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371577
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371578
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1164812604
seq_region_name: 17
source: dbSNP
start: 73371581
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371715
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73371717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73371719
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73371720
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73371722
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73371725
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371726
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371730
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371737
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371738
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371742
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371746
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371748
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371755
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371758
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371763
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371765
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371769
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371770
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73371775
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062735990
seq_region_name: 17
source: dbSNP
start: 73371777
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs780049116
seq_region_name: 17
source: dbSNP
start: 73371779
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371780
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs185191007
seq_region_name: 17
source: dbSNP
start: 73371781
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062736078
seq_region_name: 17
source: dbSNP
start: 73371782
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73371788
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs912473178
seq_region_name: 17
source: dbSNP
start: 73371789
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1341525970
seq_region_name: 17
source: dbSNP
start: 73371790
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371792
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371796
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371796
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1436357079
seq_region_name: 17
source: dbSNP
start: 73371797
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371804
feature_type: variation
id: rs1369111721
seq_region_name: 17
source: dbSNP
start: 73371804
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371805
feature_type: variation
id: rs2062736243
seq_region_name: 17
source: dbSNP
start: 73371805
strand: 1
-
alleles:
- AAAAA
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371810
feature_type: variation
id: rs1274507497
seq_region_name: 17
source: dbSNP
start: 73371806
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371810
feature_type: variation
id: rs972977730
seq_region_name: 17
source: dbSNP
start: 73371810
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371816
feature_type: variation
id: rs150297485
seq_region_name: 17
source: dbSNP
start: 73371816
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371817
feature_type: variation
id: rs369057718
seq_region_name: 17
source: dbSNP
start: 73371817
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371821
feature_type: variation
id: rs2145445308
seq_region_name: 17
source: dbSNP
start: 73371821
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371822
feature_type: variation
id: rs1048478308
seq_region_name: 17
source: dbSNP
start: 73371822
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371823
feature_type: variation
id: rs2062736370
seq_region_name: 17
source: dbSNP
start: 73371823
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371824
feature_type: variation
id: rs1369369254
seq_region_name: 17
source: dbSNP
start: 73371823
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371826
feature_type: variation
id: rs1337041733
seq_region_name: 17
source: dbSNP
start: 73371826
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371829
feature_type: variation
id: rs1211991340
seq_region_name: 17
source: dbSNP
start: 73371829
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371831
feature_type: variation
id: rs2062736468
seq_region_name: 17
source: dbSNP
start: 73371831
strand: 1
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73371911
strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371920
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73371921
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73371923
strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73371940
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73371942
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371947
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371951
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371952
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73371955
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062737588
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371957
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371958
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371971
feature_type: variation
id: rs11361484
seq_region_name: 17
source: dbSNP
start: 73371958
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371967
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371969
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371970
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73371971
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371971
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73371973
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs555072698
seq_region_name: 17
source: dbSNP
start: 73371974
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73371978
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371979
feature_type: variation
id: rs1485424375
seq_region_name: 17
source: dbSNP
start: 73371979
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1330251815
seq_region_name: 17
source: dbSNP
start: 73371982
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371986
feature_type: variation
id: rs1290694852
seq_region_name: 17
source: dbSNP
start: 73371986
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371991
feature_type: variation
id: rs2062737988
seq_region_name: 17
source: dbSNP
start: 73371991
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371993
feature_type: variation
id: rs888560611
seq_region_name: 17
source: dbSNP
start: 73371993
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371996
feature_type: variation
id: rs2062738040
seq_region_name: 17
source: dbSNP
start: 73371996
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73371997
feature_type: variation
id: rs2062738063
seq_region_name: 17
source: dbSNP
start: 73371997
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372001
feature_type: variation
id: rs1376344831
seq_region_name: 17
source: dbSNP
start: 73372001
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372006
feature_type: variation
id: rs1301791921
seq_region_name: 17
source: dbSNP
start: 73372006
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372008
feature_type: variation
id: rs1448267368
seq_region_name: 17
source: dbSNP
start: 73372008
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372014
feature_type: variation
id: rs2062738141
seq_region_name: 17
source: dbSNP
start: 73372014
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372018
feature_type: variation
id: rs2062738164
seq_region_name: 17
source: dbSNP
start: 73372018
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372025
feature_type: variation
id: rs2145445820
seq_region_name: 17
source: dbSNP
start: 73372025
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372026
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id: rs2062738185
seq_region_name: 17
source: dbSNP
start: 73372026
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372027
feature_type: variation
id: rs2062738207
seq_region_name: 17
source: dbSNP
start: 73372027
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372029
feature_type: variation
id: rs1005589240
seq_region_name: 17
source: dbSNP
start: 73372029
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372030
feature_type: variation
id: rs904690811
seq_region_name: 17
source: dbSNP
start: 73372030
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372032
feature_type: variation
id: rs958965101
seq_region_name: 17
source: dbSNP
start: 73372032
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372033
feature_type: variation
id: rs1186662606
seq_region_name: 17
source: dbSNP
start: 73372033
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372034
feature_type: variation
id: rs1412451246
seq_region_name: 17
source: dbSNP
start: 73372034
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372035
feature_type: variation
id: rs1412094711
seq_region_name: 17
source: dbSNP
start: 73372035
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372036
feature_type: variation
id: rs1000998812
seq_region_name: 17
source: dbSNP
start: 73372036
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372040
feature_type: variation
id: rs1599494380
seq_region_name: 17
source: dbSNP
start: 73372040
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372043
feature_type: variation
id: rs2062738349
seq_region_name: 17
source: dbSNP
start: 73372043
strand: 1
-
alleles:
- TCC
- TCCTCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372046
feature_type: variation
id: rs1413137590
seq_region_name: 17
source: dbSNP
start: 73372044
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372046
feature_type: variation
id: rs2062738389
seq_region_name: 17
source: dbSNP
start: 73372046
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372056
feature_type: variation
id: rs1032105007
seq_region_name: 17
source: dbSNP
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372099
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372108
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs972685415
seq_region_name: 17
source: dbSNP
start: 73372111
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs188220890
seq_region_name: 17
source: dbSNP
start: 73372112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1412993821
seq_region_name: 17
source: dbSNP
start: 73372113
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1380712766
seq_region_name: 17
source: dbSNP
start: 73372121
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1312300947
seq_region_name: 17
source: dbSNP
start: 73372123
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568369884
seq_region_name: 17
source: dbSNP
start: 73372124
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1318052279
seq_region_name: 17
source: dbSNP
start: 73372128
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062738934
seq_region_name: 17
source: dbSNP
start: 73372131
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062738955
seq_region_name: 17
source: dbSNP
start: 73372136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062738969
seq_region_name: 17
source: dbSNP
start: 73372143
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062738988
seq_region_name: 17
source: dbSNP
start: 73372144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs952595070
seq_region_name: 17
source: dbSNP
start: 73372148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1389096023
seq_region_name: 17
source: dbSNP
start: 73372152
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1322355674
seq_region_name: 17
source: dbSNP
start: 73372154
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs984583289
seq_region_name: 17
source: dbSNP
start: 73372155
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs927368426
seq_region_name: 17
source: dbSNP
start: 73372157
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372158
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1367782309
seq_region_name: 17
source: dbSNP
start: 73372159
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1165404496
seq_region_name: 17
source: dbSNP
start: 73372162
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs555060374
seq_region_name: 17
source: dbSNP
start: 73372163
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1188166091
seq_region_name: 17
source: dbSNP
start: 73372169
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372170
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062739246
seq_region_name: 17
source: dbSNP
start: 73372171
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs576431413
seq_region_name: 17
source: dbSNP
start: 73372172
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372176
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568369903
seq_region_name: 17
source: dbSNP
start: 73372180
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs917255327
seq_region_name: 17
source: dbSNP
start: 73372181
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372182
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1282350788
seq_region_name: 17
source: dbSNP
start: 73372183
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599494490
seq_region_name: 17
source: dbSNP
start: 73372187
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062739436
seq_region_name: 17
source: dbSNP
start: 73372190
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs944376022
seq_region_name: 17
source: dbSNP
start: 73372193
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73372194
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372194
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1266475901
seq_region_name: 17
source: dbSNP
start: 73372196
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1345580737
seq_region_name: 17
source: dbSNP
start: 73372197
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372198
feature_type: variation
id: rs2062739555
seq_region_name: 17
source: dbSNP
start: 73372198
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372203
feature_type: variation
id: rs1224444505
seq_region_name: 17
source: dbSNP
start: 73372203
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372204
feature_type: variation
id: rs2062739597
seq_region_name: 17
source: dbSNP
start: 73372204
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372206
feature_type: variation
id: rs1599494524
seq_region_name: 17
source: dbSNP
start: 73372206
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372207
feature_type: variation
id: rs904658696
seq_region_name: 17
source: dbSNP
start: 73372207
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372208
feature_type: variation
id: rs1040017769
seq_region_name: 17
source: dbSNP
start: 73372208
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372214
feature_type: variation
id: rs2062739680
seq_region_name: 17
source: dbSNP
start: 73372214
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372217
feature_type: variation
id: rs1227171297
seq_region_name: 17
source: dbSNP
start: 73372217
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372220
feature_type: variation
id: rs1365410490
seq_region_name: 17
source: dbSNP
start: 73372220
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372221
feature_type: variation
id: rs2062739750
seq_region_name: 17
source: dbSNP
start: 73372221
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372226
feature_type: variation
id: rs1568369932
seq_region_name: 17
source: dbSNP
start: 73372226
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372228
feature_type: variation
id: rs2062739787
seq_region_name: 17
source: dbSNP
start: 73372228
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372232
feature_type: variation
id: rs1299406724
seq_region_name: 17
source: dbSNP
start: 73372232
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372233
feature_type: variation
id: rs2062739827
seq_region_name: 17
source: dbSNP
start: 73372233
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372235
feature_type: variation
id: rs2062739849
seq_region_name: 17
source: dbSNP
start: 73372236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372236
feature_type: variation
id: rs922859485
seq_region_name: 17
source: dbSNP
start: 73372236
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372237
feature_type: variation
id: rs769586504
seq_region_name: 17
source: dbSNP
start: 73372237
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372238
feature_type: variation
id: rs374026305
seq_region_name: 17
source: dbSNP
start: 73372238
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372239
feature_type: variation
id: rs752279749
seq_region_name: 17
source: dbSNP
start: 73372239
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372240
feature_type: variation
id: rs1249463308
seq_region_name: 17
source: dbSNP
start: 73372240
strand: 1
-
alleles:
- AAA
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372245
feature_type: variation
id: rs58320926
seq_region_name: 17
source: dbSNP
start: 73372243
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372244
feature_type: variation
id: rs2062739995
seq_region_name: 17
source: dbSNP
start: 73372244
strand: 1
-
alleles:
- AAGGACATAAAGGGA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372258
feature_type: variation
id: rs2062740020
seq_region_name: 17
source: dbSNP
start: 73372244
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372245
feature_type: variation
id: rs1820323924
seq_region_name: 17
source: dbSNP
start: 73372245
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372246
feature_type: variation
id: rs2062740045
seq_region_name: 17
source: dbSNP
start: 73372246
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372247
feature_type: variation
id: rs1568369950
seq_region_name: 17
source: dbSNP
start: 73372247
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372248
feature_type: variation
id: rs1368756406
seq_region_name: 17
source: dbSNP
start: 73372248
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372257
feature_type: variation
id: rs1418827621
seq_region_name: 17
source: dbSNP
start: 73372257
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372259
feature_type: variation
id: rs2062740141
seq_region_name: 17
source: dbSNP
start: 73372259
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372260
feature_type: variation
id: rs888606577
seq_region_name: 17
source: dbSNP
start: 73372260
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372261
feature_type: variation
id: rs889539253
seq_region_name: 17
source: dbSNP
start: 73372261
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372263
feature_type: variation
id: rs2145446418
seq_region_name: 17
source: dbSNP
start: 73372263
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372265
feature_type: variation
id: rs775344331
seq_region_name: 17
source: dbSNP
start: 73372265
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73372353
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372367
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372368
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372369
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372373
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73372379
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372381
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062741499
seq_region_name: 17
source: dbSNP
start: 73372385
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372388
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372391
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372392
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2079265817
seq_region_name: 17
source: dbSNP
start: 73372397
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372398
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372403
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372404
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs957201833
seq_region_name: 17
source: dbSNP
start: 73372406
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1465787860
seq_region_name: 17
source: dbSNP
start: 73372409
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372410
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372416
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062741751
seq_region_name: 17
source: dbSNP
start: 73372418
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs985923778
seq_region_name: 17
source: dbSNP
start: 73372422
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062741806
seq_region_name: 17
source: dbSNP
start: 73372424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372425
feature_type: variation
id: rs2062741826
seq_region_name: 17
source: dbSNP
start: 73372425
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372426
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id: rs2062741850
seq_region_name: 17
source: dbSNP
start: 73372426
strand: 1
-
alleles:
- TCAATCAAT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372436
feature_type: variation
id: rs1305302598
seq_region_name: 17
source: dbSNP
start: 73372428
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372429
feature_type: variation
id: rs1368517257
seq_region_name: 17
source: dbSNP
start: 73372429
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372430
feature_type: variation
id: rs2062741934
seq_region_name: 17
source: dbSNP
start: 73372430
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372431
feature_type: variation
id: rs1178752892
seq_region_name: 17
source: dbSNP
start: 73372431
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372435
feature_type: variation
id: rs1471833535
seq_region_name: 17
source: dbSNP
start: 73372435
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372441
feature_type: variation
id: rs1233394165
seq_region_name: 17
source: dbSNP
start: 73372441
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372442
feature_type: variation
id: rs564892729
seq_region_name: 17
source: dbSNP
start: 73372442
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062742073
seq_region_name: 17
source: dbSNP
start: 73372445
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372446
feature_type: variation
id: rs1183555160
seq_region_name: 17
source: dbSNP
start: 73372446
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372451
feature_type: variation
id: rs1483091161
seq_region_name: 17
source: dbSNP
start: 73372451
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372455
feature_type: variation
id: rs2062742159
seq_region_name: 17
source: dbSNP
start: 73372455
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372456
feature_type: variation
id: rs2062742200
seq_region_name: 17
source: dbSNP
start: 73372456
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372458
feature_type: variation
id: rs2062742234
seq_region_name: 17
source: dbSNP
start: 73372457
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372465
feature_type: variation
id: rs1017385071
seq_region_name: 17
source: dbSNP
start: 73372465
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372469
feature_type: variation
id: rs965795630
seq_region_name: 17
source: dbSNP
start: 73372469
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372473
feature_type: variation
id: rs576765530
seq_region_name: 17
source: dbSNP
start: 73372473
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372477
feature_type: variation
id: rs540922121
seq_region_name: 17
source: dbSNP
start: 73372477
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372479
feature_type: variation
id: rs976182130
seq_region_name: 17
source: dbSNP
start: 73372479
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372481
feature_type: variation
id: rs2062742460
seq_region_name: 17
source: dbSNP
start: 73372481
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372484
feature_type: variation
id: rs2145446890
seq_region_name: 17
source: dbSNP
start: 73372484
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372486
feature_type: variation
id: rs2062742491
seq_region_name: 17
source: dbSNP
start: 73372486
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372496
feature_type: variation
id: rs958747312
seq_region_name: 17
source: dbSNP
start: 73372496
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372497
feature_type: variation
id: rs559310747
seq_region_name: 17
source: dbSNP
start: 73372497
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372499
feature_type: variation
id: rs1225073164
seq_region_name: 17
source: dbSNP
start: 73372499
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372502
feature_type: variation
id: rs992874230
seq_region_name: 17
source: dbSNP
start: 73372502
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372505
feature_type: variation
id: rs2062742654
seq_region_name: 17
source: dbSNP
start: 73372505
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372506
feature_type: variation
id: rs2062742686
seq_region_name: 17
source: dbSNP
start: 73372506
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062742724
seq_region_name: 17
source: dbSNP
start: 73372506
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1488576129
seq_region_name: 17
source: dbSNP
start: 73372510
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1410415220
seq_region_name: 17
source: dbSNP
start: 73372513
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1195145927
seq_region_name: 17
source: dbSNP
start: 73372516
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1255213797
seq_region_name: 17
source: dbSNP
start: 73372517
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062742874
seq_region_name: 17
source: dbSNP
start: 73372518
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs917213499
seq_region_name: 17
source: dbSNP
start: 73372519
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1403131269
seq_region_name: 17
source: dbSNP
start: 73372520
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1338949925
seq_region_name: 17
source: dbSNP
start: 73372522
strand: 1
-
alleles:
- AA
- AAA
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1455922247
seq_region_name: 17
source: dbSNP
start: 73372525
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs918911513
seq_region_name: 17
source: dbSNP
start: 73372526
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs4395139
seq_region_name: 17
source: dbSNP
start: 73372529
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs930254267
seq_region_name: 17
source: dbSNP
start: 73372530
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs4420593
seq_region_name: 17
source: dbSNP
start: 73372531
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs568598768
seq_region_name: 17
source: dbSNP
start: 73372533
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1473879193
seq_region_name: 17
source: dbSNP
start: 73372535
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372538
feature_type: variation
id: rs2062743227
seq_region_name: 17
source: dbSNP
start: 73372538
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062743263
seq_region_name: 17
source: dbSNP
start: 73372540
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs75125621
seq_region_name: 17
source: dbSNP
start: 73372541
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372542
feature_type: variation
id: rs910096340
seq_region_name: 17
source: dbSNP
start: 73372542
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs4510087
seq_region_name: 17
source: dbSNP
start: 73372545
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1256345188
seq_region_name: 17
source: dbSNP
start: 73372548
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs548054966
seq_region_name: 17
source: dbSNP
start: 73372554
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062743539
seq_region_name: 17
source: dbSNP
start: 73372559
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372560
feature_type: variation
id: rs2062743577
seq_region_name: 17
source: dbSNP
start: 73372560
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062743611
seq_region_name: 17
source: dbSNP
start: 73372565
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062743640
seq_region_name: 17
source: dbSNP
start: 73372566
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062743671
seq_region_name: 17
source: dbSNP
start: 73372567
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372568
feature_type: variation
id: rs1599494810
seq_region_name: 17
source: dbSNP
start: 73372568
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1463368573
seq_region_name: 17
source: dbSNP
start: 73372571
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372574
feature_type: variation
id: rs1267344833
seq_region_name: 17
source: dbSNP
start: 73372574
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372575
feature_type: variation
id: rs926204863
seq_region_name: 17
source: dbSNP
start: 73372575
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372578
feature_type: variation
id: rs2062743843
seq_region_name: 17
source: dbSNP
start: 73372578
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs936292339
seq_region_name: 17
source: dbSNP
start: 73372580
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1050577558
seq_region_name: 17
source: dbSNP
start: 73372584
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372585
feature_type: variation
id: rs140792474
seq_region_name: 17
source: dbSNP
start: 73372585
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372588
feature_type: variation
id: rs1352811973
seq_region_name: 17
source: dbSNP
start: 73372588
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372589
feature_type: variation
id: rs1282378656
seq_region_name: 17
source: dbSNP
start: 73372589
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372591
feature_type: variation
id: rs1354040435
seq_region_name: 17
source: dbSNP
start: 73372591
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372592
feature_type: variation
id: rs2062744074
seq_region_name: 17
source: dbSNP
start: 73372592
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372593
feature_type: variation
id: rs942389663
seq_region_name: 17
source: dbSNP
start: 73372593
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372594
feature_type: variation
id: rs2062744148
seq_region_name: 17
source: dbSNP
start: 73372594
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372596
feature_type: variation
id: rs2062744177
seq_region_name: 17
source: dbSNP
start: 73372596
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372597
feature_type: variation
id: rs767800814
seq_region_name: 17
source: dbSNP
start: 73372597
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372598
feature_type: variation
id: rs2062744249
seq_region_name: 17
source: dbSNP
start: 73372598
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372602
feature_type: variation
id: rs75413094
seq_region_name: 17
source: dbSNP
start: 73372602
strand: 1
-
alleles:
- TGGTGGTGG
- TGGTGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372611
feature_type: variation
id: rs2062744339
seq_region_name: 17
source: dbSNP
start: 73372603
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372607
feature_type: variation
id: rs900807710
seq_region_name: 17
source: dbSNP
start: 73372607
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372608
feature_type: variation
id: rs761084832
seq_region_name: 17
source: dbSNP
start: 73372608
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372609
feature_type: variation
id: rs2062744471
seq_region_name: 17
source: dbSNP
start: 73372609
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372610
feature_type: variation
id: rs1025756730
seq_region_name: 17
source: dbSNP
start: 73372610
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372612
feature_type: variation
id: rs2062744535
seq_region_name: 17
source: dbSNP
start: 73372612
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372616
feature_type: variation
id: rs2062744564
seq_region_name: 17
source: dbSNP
start: 73372616
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372622
feature_type: variation
id: rs888361909
seq_region_name: 17
source: dbSNP
start: 73372622
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372623
feature_type: variation
id: rs112676131
seq_region_name: 17
source: dbSNP
start: 73372623
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372628
feature_type: variation
id: rs2062744698
seq_region_name: 17
source: dbSNP
start: 73372628
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372631
feature_type: variation
id: rs2062744739
seq_region_name: 17
source: dbSNP
start: 73372631
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372633
feature_type: variation
id: rs374942920
seq_region_name: 17
source: dbSNP
start: 73372633
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372634
feature_type: variation
id: rs1368601940
seq_region_name: 17
source: dbSNP
start: 73372634
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372635
feature_type: variation
id: rs1321798422
seq_region_name: 17
source: dbSNP
start: 73372635
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372637
feature_type: variation
id: rs958549901
seq_region_name: 17
source: dbSNP
start: 73372637
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372639
feature_type: variation
id: rs1447328457
seq_region_name: 17
source: dbSNP
start: 73372639
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372644
feature_type: variation
id: rs2062744894
seq_region_name: 17
source: dbSNP
start: 73372644
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372645
feature_type: variation
id: rs1215113318
seq_region_name: 17
source: dbSNP
start: 73372645
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372646
feature_type: variation
id: rs1209067684
seq_region_name: 17
source: dbSNP
start: 73372646
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372655
feature_type: variation
id: rs893037577
seq_region_name: 17
source: dbSNP
start: 73372655
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372656
feature_type: variation
id: rs1209224823
seq_region_name: 17
source: dbSNP
start: 73372656
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372659
feature_type: variation
id: rs2145447372
seq_region_name: 17
source: dbSNP
start: 73372659
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372660
feature_type: variation
id: rs1357135505
seq_region_name: 17
source: dbSNP
start: 73372660
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372670
feature_type: variation
id: rs1007413891
seq_region_name: 17
source: dbSNP
start: 73372670
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372671
feature_type: variation
id: rs1599494922
seq_region_name: 17
source: dbSNP
start: 73372671
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372676
feature_type: variation
id: rs992842880
seq_region_name: 17
source: dbSNP
start: 73372676
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372678
feature_type: variation
id: rs1270950718
seq_region_name: 17
source: dbSNP
start: 73372678
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372680
feature_type: variation
id: rs2062745125
seq_region_name: 17
source: dbSNP
start: 73372680
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372681
feature_type: variation
id: rs2062745160
seq_region_name: 17
source: dbSNP
start: 73372681
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372682
feature_type: variation
id: rs767503712
seq_region_name: 17
source: dbSNP
start: 73372682
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372692
feature_type: variation
id: rs2062745232
seq_region_name: 17
source: dbSNP
start: 73372692
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372693
feature_type: variation
id: rs2062745265
seq_region_name: 17
source: dbSNP
start: 73372693
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372697
feature_type: variation
id: rs138574626
seq_region_name: 17
source: dbSNP
start: 73372697
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372699
feature_type: variation
id: rs1298643229
seq_region_name: 17
source: dbSNP
start: 73372699
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372700
feature_type: variation
id: rs967888541
seq_region_name: 17
source: dbSNP
start: 73372700
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372703
feature_type: variation
id: rs1433251151
seq_region_name: 17
source: dbSNP
start: 73372703
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372704
feature_type: variation
id: rs2062745443
seq_region_name: 17
source: dbSNP
start: 73372704
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372711
feature_type: variation
id: rs2062745466
seq_region_name: 17
source: dbSNP
start: 73372711
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372714
feature_type: variation
id: rs2062745503
seq_region_name: 17
source: dbSNP
start: 73372714
strand: 1
-
alleles:
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- GG
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372781
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372789
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73372794
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372795
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372806
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372808
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372815
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73372817
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062747182
seq_region_name: 17
source: dbSNP
start: 73372818
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372819
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372820
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73372821
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1346780121
seq_region_name: 17
source: dbSNP
start: 73372824
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs888111615
seq_region_name: 17
source: dbSNP
start: 73372829
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73372830
feature_type: variation
id: rs2062747400
seq_region_name: 17
source: dbSNP
start: 73372830
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1005400964
seq_region_name: 17
source: dbSNP
start: 73372831
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372834
feature_type: variation
id: rs1568370198
seq_region_name: 17
source: dbSNP
start: 73372834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372836
feature_type: variation
id: rs1599495115
seq_region_name: 17
source: dbSNP
start: 73372836
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372838
feature_type: variation
id: rs2062747532
seq_region_name: 17
source: dbSNP
start: 73372838
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73372840
feature_type: variation
id: rs183581234
seq_region_name: 17
source: dbSNP
start: 73372840
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372847
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73372847
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs934669327
seq_region_name: 17
source: dbSNP
start: 73372850
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372852
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id: rs1220138216
seq_region_name: 17
source: dbSNP
start: 73372852
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062747721
seq_region_name: 17
source: dbSNP
start: 73372853
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73372854
feature_type: variation
id: rs2062747777
seq_region_name: 17
source: dbSNP
start: 73372854
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372855
feature_type: variation
id: rs1234669236
seq_region_name: 17
source: dbSNP
start: 73372855
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73372858
feature_type: variation
id: rs2062747854
seq_region_name: 17
source: dbSNP
start: 73372858
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372863
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id: rs1286987830
seq_region_name: 17
source: dbSNP
start: 73372863
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372864
feature_type: variation
id: rs2062747925
seq_region_name: 17
source: dbSNP
start: 73372864
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372873
feature_type: variation
id: rs757267615
seq_region_name: 17
source: dbSNP
start: 73372873
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372874
feature_type: variation
id: rs1054431468
seq_region_name: 17
source: dbSNP
start: 73372874
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372884
feature_type: variation
id: rs2062748001
seq_region_name: 17
source: dbSNP
start: 73372877
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372878
feature_type: variation
id: rs1333768642
seq_region_name: 17
source: dbSNP
start: 73372878
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372882
feature_type: variation
id: rs2062748091
seq_region_name: 17
source: dbSNP
start: 73372882
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372882
feature_type: variation
id: rs2062748137
seq_region_name: 17
source: dbSNP
start: 73372882
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372883
feature_type: variation
id: rs893088256
seq_region_name: 17
source: dbSNP
start: 73372883
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372886
feature_type: variation
id: rs781078441
seq_region_name: 17
source: dbSNP
start: 73372886
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372888
feature_type: variation
id: rs576802030
seq_region_name: 17
source: dbSNP
start: 73372888
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372892
feature_type: variation
id: rs1214253292
seq_region_name: 17
source: dbSNP
start: 73372892
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372895
feature_type: variation
id: rs1431243565
seq_region_name: 17
source: dbSNP
start: 73372895
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372907
feature_type: variation
id: rs2062748282
seq_region_name: 17
source: dbSNP
start: 73372907
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372911
feature_type: variation
id: rs558624354
seq_region_name: 17
source: dbSNP
start: 73372911
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372918
feature_type: variation
id: rs1242112441
seq_region_name: 17
source: dbSNP
start: 73372918
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73372919
feature_type: variation
id: rs1014022256
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source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73373027
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73373036
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73373041
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73373042
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73373043
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73373054
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73373055
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373067
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373068
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373069
strand: 1
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373075
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373076
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373078
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373079
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373084
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373086
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062750472
seq_region_name: 17
source: dbSNP
start: 73373088
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373092
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373097
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373104
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145448330
seq_region_name: 17
source: dbSNP
start: 73373105
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373106
feature_type: variation
id: rs941015416
seq_region_name: 17
source: dbSNP
start: 73373106
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373107
feature_type: variation
id: rs1054484567
seq_region_name: 17
source: dbSNP
start: 73373107
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs748627946
seq_region_name: 17
source: dbSNP
start: 73373108
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373119
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373122
feature_type: variation
id: rs1234882111
seq_region_name: 17
source: dbSNP
start: 73373122
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373123
feature_type: variation
id: rs2062750717
seq_region_name: 17
source: dbSNP
start: 73373123
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373127
feature_type: variation
id: rs2062750733
seq_region_name: 17
source: dbSNP
start: 73373127
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373128
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373129
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373129
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373134
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373134
strand: 1
-
alleles:
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- TGCTTGCTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373140
feature_type: variation
id: rs1157835795
seq_region_name: 17
source: dbSNP
start: 73373135
strand: 1
-
alleles:
- A
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73373228
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73373240
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73373295
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373300
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73373301
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373302
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373303
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373314
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373322
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373326
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373334
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373335
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373336
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373340
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373340
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373341
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73373344
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373344
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373348
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373356
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373358
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373360
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1455464191
seq_region_name: 17
source: dbSNP
start: 73373362
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373363
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373378
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373381
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373383
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373390
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373392
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373393
feature_type: variation
id: rs1471924403
seq_region_name: 17
source: dbSNP
start: 73373393
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73373394
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062752583
seq_region_name: 17
source: dbSNP
start: 73373395
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373396
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373397
feature_type: variation
id: rs2145448851
seq_region_name: 17
source: dbSNP
start: 73373397
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373401
feature_type: variation
id: rs924754955
seq_region_name: 17
source: dbSNP
start: 73373401
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373403
feature_type: variation
id: rs1180412124
seq_region_name: 17
source: dbSNP
start: 73373403
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373409
feature_type: variation
id: rs1419156788
seq_region_name: 17
source: dbSNP
start: 73373409
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373419
feature_type: variation
id: rs2062752680
seq_region_name: 17
source: dbSNP
start: 73373419
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373424
feature_type: variation
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73373606
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1054319127
seq_region_name: 17
source: dbSNP
start: 73373610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373611
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373612
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373616
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1271965303
seq_region_name: 17
source: dbSNP
start: 73373620
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73373623
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062754108
seq_region_name: 17
source: dbSNP
start: 73373627
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062754125
seq_region_name: 17
source: dbSNP
start: 73373628
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373630
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373637
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754184
seq_region_name: 17
source: dbSNP
start: 73373642
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145449244
seq_region_name: 17
source: dbSNP
start: 73373647
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1423488160
seq_region_name: 17
source: dbSNP
start: 73373649
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373651
feature_type: variation
id: rs1017576954
seq_region_name: 17
source: dbSNP
start: 73373651
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73373652
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id: rs2062754234
seq_region_name: 17
source: dbSNP
start: 73373652
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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end: 73373653
feature_type: variation
id: rs1165102823
seq_region_name: 17
source: dbSNP
start: 73373653
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373654
feature_type: variation
id: rs1241373255
seq_region_name: 17
source: dbSNP
start: 73373654
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373660
feature_type: variation
id: rs1011930622
seq_region_name: 17
source: dbSNP
start: 73373654
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373663
feature_type: variation
id: rs1599495794
seq_region_name: 17
source: dbSNP
start: 73373663
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1193773058
seq_region_name: 17
source: dbSNP
start: 73373665
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1265217824
seq_region_name: 17
source: dbSNP
start: 73373665
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754382
seq_region_name: 17
source: dbSNP
start: 73373666
strand: 1
-
alleles:
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- TTTT
- TTTTTTTT
- TTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373674
feature_type: variation
id: rs201908475
seq_region_name: 17
source: dbSNP
start: 73373666
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373667
feature_type: variation
id: rs1360273792
seq_region_name: 17
source: dbSNP
start: 73373667
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373668
feature_type: variation
id: rs2062754470
seq_region_name: 17
source: dbSNP
start: 73373668
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373669
feature_type: variation
id: rs2062754493
seq_region_name: 17
source: dbSNP
start: 73373669
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373670
feature_type: variation
id: rs2062754511
seq_region_name: 17
source: dbSNP
start: 73373670
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373673
feature_type: variation
id: rs907476452
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73373675
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373681
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs901861822
seq_region_name: 17
source: dbSNP
start: 73373683
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs997749576
seq_region_name: 17
source: dbSNP
start: 73373684
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1003534972
seq_region_name: 17
source: dbSNP
start: 73373691
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs58025350
seq_region_name: 17
source: dbSNP
start: 73373692
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1303089385
seq_region_name: 17
source: dbSNP
start: 73373693
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1403737305
seq_region_name: 17
source: dbSNP
start: 73373698
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754745
seq_region_name: 17
source: dbSNP
start: 73373699
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs60999191
seq_region_name: 17
source: dbSNP
start: 73373701
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754795
seq_region_name: 17
source: dbSNP
start: 73373702
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1365722767
seq_region_name: 17
source: dbSNP
start: 73373703
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145449425
seq_region_name: 17
source: dbSNP
start: 73373708
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs956201559
seq_region_name: 17
source: dbSNP
start: 73373709
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754867
seq_region_name: 17
source: dbSNP
start: 73373710
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754888
seq_region_name: 17
source: dbSNP
start: 73373710
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062754911
seq_region_name: 17
source: dbSNP
start: 73373713
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599495876
seq_region_name: 17
source: dbSNP
start: 73373716
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1407900248
seq_region_name: 17
source: dbSNP
start: 73373719
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062754974
seq_region_name: 17
source: dbSNP
start: 73373720
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs776864960
seq_region_name: 17
source: dbSNP
start: 73373721
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs951018582
seq_region_name: 17
source: dbSNP
start: 73373724
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145449481
seq_region_name: 17
source: dbSNP
start: 73373725
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062755035
seq_region_name: 17
source: dbSNP
start: 73373727
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1168241499
seq_region_name: 17
source: dbSNP
start: 73373732
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1195243328
seq_region_name: 17
source: dbSNP
start: 73373733
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145449502
seq_region_name: 17
source: dbSNP
start: 73373735
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599495897
seq_region_name: 17
source: dbSNP
start: 73373737
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062755122
seq_region_name: 17
source: dbSNP
start: 73373741
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373743
feature_type: variation
id: rs985358486
seq_region_name: 17
source: dbSNP
start: 73373743
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062755175
seq_region_name: 17
source: dbSNP
start: 73373744
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1370786226
seq_region_name: 17
source: dbSNP
start: 73373751
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1427045097
seq_region_name: 17
source: dbSNP
start: 73373752
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs759709018
seq_region_name: 17
source: dbSNP
start: 73373757
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs962400489
seq_region_name: 17
source: dbSNP
start: 73373759
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1021730579
seq_region_name: 17
source: dbSNP
start: 73373760
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062755316
seq_region_name: 17
source: dbSNP
start: 73373761
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1271187101
seq_region_name: 17
source: dbSNP
start: 73373767
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs965142900
seq_region_name: 17
source: dbSNP
start: 73373776
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1437410241
seq_region_name: 17
source: dbSNP
start: 73373778
strand: 1
-
alleles:
- AGGT
- AGGTAGGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373781
feature_type: variation
id: rs2062755406
seq_region_name: 17
source: dbSNP
start: 73373778
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1165190324
seq_region_name: 17
source: dbSNP
start: 73373788
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1216628023
seq_region_name: 17
source: dbSNP
start: 73373789
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs974793954
seq_region_name: 17
source: dbSNP
start: 73373793
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373794
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs991203159
seq_region_name: 17
source: dbSNP
start: 73373796
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs923260034
seq_region_name: 17
source: dbSNP
start: 73373799
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1439423534
seq_region_name: 17
source: dbSNP
start: 73373808
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs933284550
seq_region_name: 17
source: dbSNP
start: 73373809
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373815
feature_type: variation
id: rs2062755580
seq_region_name: 17
source: dbSNP
start: 73373815
strand: 1
-
alleles:
- GAGACG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs763276789
seq_region_name: 17
source: dbSNP
start: 73373821
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373825
feature_type: variation
id: rs765296099
seq_region_name: 17
source: dbSNP
start: 73373825
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373826
feature_type: variation
id: rs528145910
seq_region_name: 17
source: dbSNP
start: 73373826
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373828
feature_type: variation
id: rs983337953
seq_region_name: 17
source: dbSNP
start: 73373828
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373830
feature_type: variation
id: rs1480749838
seq_region_name: 17
source: dbSNP
start: 73373830
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373839
feature_type: variation
id: rs1431378180
seq_region_name: 17
source: dbSNP
start: 73373839
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1175517532
seq_region_name: 17
source: dbSNP
start: 73373842
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373843
feature_type: variation
id: rs2062755768
seq_region_name: 17
source: dbSNP
start: 73373843
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373845
feature_type: variation
id: rs1390507918
seq_region_name: 17
source: dbSNP
start: 73373845
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373848
feature_type: variation
id: rs532005853
seq_region_name: 17
source: dbSNP
start: 73373848
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373851
feature_type: variation
id: rs1206963809
seq_region_name: 17
source: dbSNP
start: 73373851
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373854
feature_type: variation
id: rs907759365
seq_region_name: 17
source: dbSNP
start: 73373854
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373855
feature_type: variation
id: rs2062755848
seq_region_name: 17
source: dbSNP
start: 73373855
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373856
feature_type: variation
id: rs139737359
seq_region_name: 17
source: dbSNP
start: 73373856
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373857
feature_type: variation
id: rs1320916712
seq_region_name: 17
source: dbSNP
start: 73373857
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373860
feature_type: variation
id: rs1326213910
seq_region_name: 17
source: dbSNP
start: 73373860
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373861
feature_type: variation
id: rs1287007762
seq_region_name: 17
source: dbSNP
start: 73373861
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373862
feature_type: variation
id: rs1221514458
seq_region_name: 17
source: dbSNP
start: 73373862
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373863
feature_type: variation
id: rs2062755968
seq_region_name: 17
source: dbSNP
start: 73373863
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373864
feature_type: variation
id: rs1324755296
seq_region_name: 17
source: dbSNP
start: 73373864
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373865
feature_type: variation
id: rs1372054625
seq_region_name: 17
source: dbSNP
start: 73373865
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373867
feature_type: variation
id: rs111991666
seq_region_name: 17
source: dbSNP
start: 73373867
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373868
feature_type: variation
id: rs1279764840
seq_region_name: 17
source: dbSNP
start: 73373867
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373868
feature_type: variation
id: rs934635854
seq_region_name: 17
source: dbSNP
start: 73373868
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373870
feature_type: variation
id: rs530469878
seq_region_name: 17
source: dbSNP
start: 73373870
strand: 1
-
alleles:
- CAGGTG
- CAGGTGCAGGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373875
feature_type: variation
id: rs1337159986
seq_region_name: 17
source: dbSNP
start: 73373870
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373872
feature_type: variation
id: rs2062756149
seq_region_name: 17
source: dbSNP
start: 73373872
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373873
feature_type: variation
id: rs2062756171
seq_region_name: 17
source: dbSNP
start: 73373873
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373877
feature_type: variation
id: rs1037470814
seq_region_name: 17
source: dbSNP
start: 73373877
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373882
feature_type: variation
id: rs1156856724
seq_region_name: 17
source: dbSNP
start: 73373881
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373883
feature_type: variation
id: rs59262719
seq_region_name: 17
source: dbSNP
start: 73373883
strand: 1
-
alleles:
- TA
- CG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373884
feature_type: variation
id: rs796954314
seq_region_name: 17
source: dbSNP
start: 73373883
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373884
feature_type: variation
id: rs58186903
seq_region_name: 17
source: dbSNP
start: 73373884
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373887
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373889
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73373891
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062756383
seq_region_name: 17
source: dbSNP
start: 73373891
strand: 1
-
alleles:
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- GC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs386799013
seq_region_name: 17
source: dbSNP
start: 73373891
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1294461070
seq_region_name: 17
source: dbSNP
start: 73373892
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062756472
seq_region_name: 17
source: dbSNP
start: 73373894
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs767560608
seq_region_name: 17
source: dbSNP
start: 73373900
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs112377699
seq_region_name: 17
source: dbSNP
start: 73373911
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1390734535
seq_region_name: 17
source: dbSNP
start: 73373916
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1474001037
seq_region_name: 17
source: dbSNP
start: 73373916
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373917
feature_type: variation
id: rs1385582030
seq_region_name: 17
source: dbSNP
start: 73373917
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1315775666
seq_region_name: 17
source: dbSNP
start: 73373918
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062756747
seq_region_name: 17
source: dbSNP
start: 73373925
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs4969115
seq_region_name: 17
source: dbSNP
start: 73373926
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs552308610
seq_region_name: 17
source: dbSNP
start: 73373927
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1380067483
seq_region_name: 17
source: dbSNP
start: 73373930
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062756824
seq_region_name: 17
source: dbSNP
start: 73373936
strand: 1
-
alleles:
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- CTGATTTGTTAGCAAATTCT
- CTGATTTGTTAGCAAATTCTACCAGCT
- CTGATTTGTTAGCAAATTCTACCAGCTCTGCTGTTGGGACT
- CTGATTTGTTAGCAAATTCTACCAGCTCTGCTGTTGGGACTAACT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373937
feature_type: variation
id: rs2062756867
seq_region_name: 17
source: dbSNP
start: 73373936
strand: 1
-
alleles:
- T
- TGATTTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062756922
seq_region_name: 17
source: dbSNP
start: 73373937
strand: 1
-
alleles:
- "-"
- G
- GATTTGTTAGC
- GATTTGTTAGCA
- GATTTGTTAGCAA
- GATTTGTTAGCAAATTCTACC
- GATTTGTTAGCAAATTCTACCAGCTCTGCTGTTGGGACTAACTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1383494783
seq_region_name: 17
source: dbSNP
start: 73373938
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599496129
seq_region_name: 17
source: dbSNP
start: 73373938
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs780631554
seq_region_name: 17
source: dbSNP
start: 73373939
strand: 1
-
alleles:
- T
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- TTTGTTAGCAAATTCTACCAGCTCT
- TTTGTTAGCAAATTCTACCAGCTCTGCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1399952854
seq_region_name: 17
source: dbSNP
start: 73373939
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1357450294
seq_region_name: 17
source: dbSNP
start: 73373940
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1026351578
seq_region_name: 17
source: dbSNP
start: 73373941
strand: 1
-
alleles:
- TCTTCTT
- TCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1413099764
seq_region_name: 17
source: dbSNP
start: 73373943
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062757149
seq_region_name: 17
source: dbSNP
start: 73373945
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062757191
seq_region_name: 17
source: dbSNP
start: 73373946
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs886680729
seq_region_name: 17
source: dbSNP
start: 73373952
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062757257
seq_region_name: 17
source: dbSNP
start: 73373954
strand: 1
-
alleles:
- ATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373959
feature_type: variation
id: rs1287047814
seq_region_name: 17
source: dbSNP
start: 73373957
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145450067
seq_region_name: 17
source: dbSNP
start: 73373958
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373959
feature_type: variation
id: rs2062757325
seq_region_name: 17
source: dbSNP
start: 73373959
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373971
feature_type: variation
id: rs2062757352
seq_region_name: 17
source: dbSNP
start: 73373971
strand: 1
-
alleles:
- TTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062757382
seq_region_name: 17
source: dbSNP
start: 73373973
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373975
feature_type: variation
id: rs570623588
seq_region_name: 17
source: dbSNP
start: 73373975
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373977
feature_type: variation
id: rs947777421
seq_region_name: 17
source: dbSNP
start: 73373977
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373978
feature_type: variation
id: rs1312351275
seq_region_name: 17
source: dbSNP
start: 73373978
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373980
feature_type: variation
id: rs534801871
seq_region_name: 17
source: dbSNP
start: 73373980
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373990
feature_type: variation
id: rs1568370592
seq_region_name: 17
source: dbSNP
start: 73373990
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73373996
feature_type: variation
id: rs1161319156
seq_region_name: 17
source: dbSNP
start: 73373996
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374000
feature_type: variation
id: rs547019689
seq_region_name: 17
source: dbSNP
start: 73374000
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374001
feature_type: variation
id: rs1384777845
seq_region_name: 17
source: dbSNP
start: 73374001
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374002
feature_type: variation
id: rs2062757650
seq_region_name: 17
source: dbSNP
start: 73374002
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374012
feature_type: variation
id: rs1164511058
seq_region_name: 17
source: dbSNP
start: 73374012
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374025
feature_type: variation
id: rs1446816296
seq_region_name: 17
source: dbSNP
start: 73374025
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374031
feature_type: variation
id: rs879301487
seq_region_name: 17
source: dbSNP
start: 73374031
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374032
feature_type: variation
id: rs2062757712
seq_region_name: 17
source: dbSNP
start: 73374032
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374037
feature_type: variation
id: rs906184240
seq_region_name: 17
source: dbSNP
start: 73374037
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374038
feature_type: variation
id: rs2062757728
seq_region_name: 17
source: dbSNP
start: 73374038
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374039
feature_type: variation
id: rs191328838
seq_region_name: 17
source: dbSNP
start: 73374039
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374041
feature_type: variation
id: rs2145450174
seq_region_name: 17
source: dbSNP
start: 73374041
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374045
feature_type: variation
id: rs1815659627
seq_region_name: 17
source: dbSNP
start: 73374045
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374047
feature_type: variation
id: rs1244362886
seq_region_name: 17
source: dbSNP
start: 73374047
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374049
feature_type: variation
id: rs2062757804
seq_region_name: 17
source: dbSNP
start: 73374049
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374050
feature_type: variation
id: rs1218079839
seq_region_name: 17
source: dbSNP
start: 73374050
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374053
feature_type: variation
id: rs999167308
seq_region_name: 17
source: dbSNP
start: 73374053
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374054
feature_type: variation
id: rs2062757871
seq_region_name: 17
source: dbSNP
start: 73374054
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374063
feature_type: variation
id: rs2062757897
seq_region_name: 17
source: dbSNP
start: 73374063
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374064
feature_type: variation
id: rs2062757919
seq_region_name: 17
source: dbSNP
start: 73374064
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374077
feature_type: variation
id: rs2062757939
seq_region_name: 17
source: dbSNP
start: 73374077
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374086
feature_type: variation
id: rs4969116
seq_region_name: 17
source: dbSNP
start: 73374086
strand: 1
-
alleles:
- CTTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374091
feature_type: variation
id: rs1246348114
seq_region_name: 17
source: dbSNP
start: 73374087
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374091
feature_type: variation
id: rs1323259176
seq_region_name: 17
source: dbSNP
start: 73374091
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374101
feature_type: variation
id: rs1293238306
seq_region_name: 17
source: dbSNP
start: 73374101
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374104
feature_type: variation
id: rs1599496227
seq_region_name: 17
source: dbSNP
start: 73374104
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374106
feature_type: variation
id: rs2062758039
seq_region_name: 17
source: dbSNP
start: 73374106
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374110
feature_type: variation
id: rs2062758065
seq_region_name: 17
source: dbSNP
start: 73374110
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374113
feature_type: variation
id: rs1031945586
seq_region_name: 17
source: dbSNP
start: 73374113
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374121
feature_type: variation
id: rs1599496237
seq_region_name: 17
source: dbSNP
start: 73374121
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374123
feature_type: variation
id: rs1022658776
seq_region_name: 17
source: dbSNP
start: 73374123
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374124
feature_type: variation
id: rs2062758116
seq_region_name: 17
source: dbSNP
start: 73374124
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374130
feature_type: variation
id: rs2062758142
seq_region_name: 17
source: dbSNP
start: 73374130
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374136
feature_type: variation
id: rs1211553480
seq_region_name: 17
source: dbSNP
start: 73374136
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374138
feature_type: variation
id: rs2062758185
seq_region_name: 17
source: dbSNP
start: 73374138
strand: 1
-
alleles:
- GGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374146
feature_type: variation
id: rs1258925578
seq_region_name: 17
source: dbSNP
start: 73374144
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374147
feature_type: variation
id: rs2062758210
seq_region_name: 17
source: dbSNP
start: 73374147
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374155
feature_type: variation
id: rs2062758237
seq_region_name: 17
source: dbSNP
start: 73374155
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374156
feature_type: variation
id: rs2062758257
seq_region_name: 17
source: dbSNP
start: 73374156
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374159
feature_type: variation
id: rs748901562
seq_region_name: 17
source: dbSNP
start: 73374159
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374160
feature_type: variation
id: rs2062758293
seq_region_name: 17
source: dbSNP
start: 73374160
strand: 1
-
alleles:
- CTTCTT
- CTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374165
feature_type: variation
id: rs892021885
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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-
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062758789
seq_region_name: 17
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start: 73374222
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374226
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374230
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1197963783
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374240
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145450503
seq_region_name: 17
source: dbSNP
start: 73374251
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062758967
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374261
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1249292914
seq_region_name: 17
source: dbSNP
start: 73374266
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs531109366
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs78370738
seq_region_name: 17
source: dbSNP
start: 73374269
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374270
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374275
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1302452992
seq_region_name: 17
source: dbSNP
start: 73374278
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374282
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374284
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374287
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062759216
seq_region_name: 17
source: dbSNP
start: 73374288
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374291
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062759270
seq_region_name: 17
source: dbSNP
start: 73374295
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062759289
seq_region_name: 17
source: dbSNP
start: 73374299
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1393383846
seq_region_name: 17
source: dbSNP
start: 73374303
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1038909173
seq_region_name: 17
source: dbSNP
start: 73374304
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1280010541
seq_region_name: 17
source: dbSNP
start: 73374305
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs923346448
seq_region_name: 17
source: dbSNP
start: 73374308
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062759414
seq_region_name: 17
source: dbSNP
start: 73374309
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374310
feature_type: variation
id: rs551228214
seq_region_name: 17
source: dbSNP
start: 73374310
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145450625
seq_region_name: 17
source: dbSNP
start: 73374317
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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end: 73374319
feature_type: variation
id: rs773696059
seq_region_name: 17
source: dbSNP
start: 73374319
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374320
feature_type: variation
id: rs941942411
seq_region_name: 17
source: dbSNP
start: 73374320
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062759521
seq_region_name: 17
source: dbSNP
start: 73374329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs149770189
seq_region_name: 17
source: dbSNP
start: 73374329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73374331
feature_type: variation
id: rs1599496376
seq_region_name: 17
source: dbSNP
start: 73374331
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374334
feature_type: variation
id: rs1599496379
seq_region_name: 17
source: dbSNP
start: 73374334
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374334
feature_type: variation
id: rs2062759700
seq_region_name: 17
source: dbSNP
start: 73374334
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1345075709
seq_region_name: 17
source: dbSNP
start: 73374335
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062759771
seq_region_name: 17
source: dbSNP
start: 73374341
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374345
feature_type: variation
id: rs1297832305
seq_region_name: 17
source: dbSNP
start: 73374345
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374357
feature_type: variation
id: rs2145450688
seq_region_name: 17
source: dbSNP
start: 73374357
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374365
feature_type: variation
id: rs1462805705
seq_region_name: 17
source: dbSNP
start: 73374365
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374366
feature_type: variation
id: rs2062759875
seq_region_name: 17
source: dbSNP
start: 73374366
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374368
feature_type: variation
id: rs2062759904
seq_region_name: 17
source: dbSNP
start: 73374368
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374372
feature_type: variation
id: rs2062759935
seq_region_name: 17
source: dbSNP
start: 73374372
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374375
feature_type: variation
id: rs886442496
seq_region_name: 17
source: dbSNP
start: 73374375
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374379
feature_type: variation
id: rs2062760000
seq_region_name: 17
source: dbSNP
start: 73374379
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374389
feature_type: variation
id: rs1006407162
seq_region_name: 17
source: dbSNP
start: 73374389
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374396
feature_type: variation
id: rs1037932053
seq_region_name: 17
source: dbSNP
start: 73374396
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374397
feature_type: variation
id: rs2062760091
seq_region_name: 17
source: dbSNP
start: 73374397
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374401
feature_type: variation
id: rs2062760121
seq_region_name: 17
source: dbSNP
start: 73374401
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374406
feature_type: variation
id: rs1174868575
seq_region_name: 17
source: dbSNP
start: 73374406
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374412
feature_type: variation
id: rs1599496403
seq_region_name: 17
source: dbSNP
start: 73374412
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374413
feature_type: variation
id: rs2062760222
seq_region_name: 17
source: dbSNP
start: 73374413
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374418
feature_type: variation
id: rs1599496407
seq_region_name: 17
source: dbSNP
start: 73374418
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374423
feature_type: variation
id: rs2062760292
seq_region_name: 17
source: dbSNP
start: 73374423
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374432
feature_type: variation
id: rs2062760330
seq_region_name: 17
source: dbSNP
start: 73374432
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374440
feature_type: variation
id: rs1480427396
seq_region_name: 17
source: dbSNP
start: 73374440
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374445
feature_type: variation
id: rs11650860
seq_region_name: 17
source: dbSNP
start: 73374445
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374448
feature_type: variation
id: rs1599496427
seq_region_name: 17
source: dbSNP
start: 73374448
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374450
feature_type: variation
id: rs1199459554
seq_region_name: 17
source: dbSNP
start: 73374450
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374451
feature_type: variation
id: rs2062760526
seq_region_name: 17
source: dbSNP
start: 73374451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374452
feature_type: variation
id: rs1251403151
seq_region_name: 17
source: dbSNP
start: 73374452
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374453
feature_type: variation
id: rs1599496441
seq_region_name: 17
source: dbSNP
start: 73374453
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374454
feature_type: variation
id: rs1481386210
seq_region_name: 17
source: dbSNP
start: 73374454
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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- TTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374478
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1439531414
seq_region_name: 17
source: dbSNP
start: 73374486
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs1469639077
seq_region_name: 17
source: dbSNP
start: 73374494
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374498
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374499
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374500
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374501
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1419252185
seq_region_name: 17
source: dbSNP
start: 73374509
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374514
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374516
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73374517
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs771259986
seq_region_name: 17
source: dbSNP
start: 73374519
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374526
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1463663246
seq_region_name: 17
source: dbSNP
start: 73374527
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs989843070
seq_region_name: 17
source: dbSNP
start: 73374528
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73374529
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1348593669
seq_region_name: 17
source: dbSNP
start: 73374530
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062761513
seq_region_name: 17
source: dbSNP
start: 73374533
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062761532
seq_region_name: 17
source: dbSNP
start: 73374535
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374536
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs537494040
seq_region_name: 17
source: dbSNP
start: 73374537
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374549
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145451213
seq_region_name: 17
source: dbSNP
start: 73374553
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062761617
seq_region_name: 17
source: dbSNP
start: 73374556
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374558
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062761637
seq_region_name: 17
source: dbSNP
start: 73374560
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73374561
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374569
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374573
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374577
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1441414832
seq_region_name: 17
source: dbSNP
start: 73374578
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374579
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs1305505310
seq_region_name: 17
source: dbSNP
start: 73374581
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs558638098
seq_region_name: 17
source: dbSNP
start: 73374582
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374584
feature_type: variation
id: rs2062761835
seq_region_name: 17
source: dbSNP
start: 73374584
strand: 1
-
alleles:
- TCCCCAGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062761850
seq_region_name: 17
source: dbSNP
start: 73374589
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1218605310
seq_region_name: 17
source: dbSNP
start: 73374592
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1295590995
seq_region_name: 17
source: dbSNP
start: 73374593
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062761929
seq_region_name: 17
source: dbSNP
start: 73374595
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs964660240
seq_region_name: 17
source: dbSNP
start: 73374596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062761981
seq_region_name: 17
source: dbSNP
start: 73374597
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1308761032
seq_region_name: 17
source: dbSNP
start: 73374599
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062762027
seq_region_name: 17
source: dbSNP
start: 73374601
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374611
feature_type: variation
id: rs2062762054
seq_region_name: 17
source: dbSNP
start: 73374601
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062762078
seq_region_name: 17
source: dbSNP
start: 73374602
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374603
feature_type: variation
id: rs1201988447
seq_region_name: 17
source: dbSNP
start: 73374603
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374610
feature_type: variation
id: rs776890515
seq_region_name: 17
source: dbSNP
start: 73374610
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374611
feature_type: variation
id: rs1457574422
seq_region_name: 17
source: dbSNP
start: 73374611
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374612
feature_type: variation
id: rs563644068
seq_region_name: 17
source: dbSNP
start: 73374612
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374613
feature_type: variation
id: rs2062762189
seq_region_name: 17
source: dbSNP
start: 73374613
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374614
feature_type: variation
id: rs906243828
seq_region_name: 17
source: dbSNP
start: 73374614
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374616
feature_type: variation
id: rs1243572258
seq_region_name: 17
source: dbSNP
start: 73374616
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374616
feature_type: variation
id: rs2062762246
seq_region_name: 17
source: dbSNP
start: 73374616
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374617
feature_type: variation
id: rs1214762118
seq_region_name: 17
source: dbSNP
start: 73374617
strand: 1
-
alleles:
- CTAC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374621
feature_type: variation
id: rs2062762289
seq_region_name: 17
source: dbSNP
start: 73374618
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374619
feature_type: variation
id: rs934996801
seq_region_name: 17
source: dbSNP
start: 73374619
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374621
feature_type: variation
id: rs1260998866
seq_region_name: 17
source: dbSNP
start: 73374621
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374624
feature_type: variation
id: rs2062762344
seq_region_name: 17
source: dbSNP
start: 73374624
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374625
feature_type: variation
id: rs1205725644
seq_region_name: 17
source: dbSNP
start: 73374625
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374626
feature_type: variation
id: rs1489321704
seq_region_name: 17
source: dbSNP
start: 73374626
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374628
feature_type: variation
id: rs2062762425
seq_region_name: 17
source: dbSNP
start: 73374628
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374630
feature_type: variation
id: rs2145451461
seq_region_name: 17
source: dbSNP
start: 73374630
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374721
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374750
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374757
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374758
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374766
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374772
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374775
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374780
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73374790
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73374791
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73374797
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374800
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374803
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374805
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374806
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374810
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374812
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374813
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73374815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73374816
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374823
feature_type: variation
id: rs1411338964
seq_region_name: 17
source: dbSNP
start: 73374823
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374830
feature_type: variation
id: rs2062764387
seq_region_name: 17
source: dbSNP
start: 73374830
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374833
feature_type: variation
id: rs1404619277
seq_region_name: 17
source: dbSNP
start: 73374833
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374841
feature_type: variation
id: rs1222318049
seq_region_name: 17
source: dbSNP
start: 73374841
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73374842
feature_type: variation
id: rs2062764455
seq_region_name: 17
source: dbSNP
start: 73374842
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73375005
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73375006
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375008
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375009
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73375011
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375014
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375015
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375019
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375023
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375025
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375026
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375030
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375033
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375034
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375040
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375045
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375046
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375050
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375051
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062766085
seq_region_name: 17
source: dbSNP
start: 73375052
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs147226038
seq_region_name: 17
source: dbSNP
start: 73375054
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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end: 73375054
feature_type: variation
id: rs2062766147
seq_region_name: 17
source: dbSNP
start: 73375054
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375054
feature_type: variation
id: rs2062766169
seq_region_name: 17
source: dbSNP
start: 73375055
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375055
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375056
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375056
feature_type: variation
id: rs2062766235
seq_region_name: 17
source: dbSNP
start: 73375056
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
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-
alleles:
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-
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375110
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375116
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375116
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73375128
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375130
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375132
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375137
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375140
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375141
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs868475934
seq_region_name: 17
source: dbSNP
start: 73375142
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375143
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375152
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375153
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375155
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1053071351
seq_region_name: 17
source: dbSNP
start: 73375156
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375158
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062767227
seq_region_name: 17
source: dbSNP
start: 73375159
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375163
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375164
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375168
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062767320
seq_region_name: 17
source: dbSNP
start: 73375173
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375179
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375191
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375193
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145453105
seq_region_name: 17
source: dbSNP
start: 73375194
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375195
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375198
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375201
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1403182932
seq_region_name: 17
source: dbSNP
start: 73375203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375206
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs969318830
seq_region_name: 17
source: dbSNP
start: 73375209
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1011336417
seq_region_name: 17
source: dbSNP
start: 73375211
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375214
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062767527
seq_region_name: 17
source: dbSNP
start: 73375221
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375222
feature_type: variation
id: rs1294395707
seq_region_name: 17
source: dbSNP
start: 73375222
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375223
feature_type: variation
id: rs1459761546
seq_region_name: 17
source: dbSNP
start: 73375223
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375223
feature_type: variation
id: rs2145453219
seq_region_name: 17
source: dbSNP
start: 73375223
strand: 1
-
alleles:
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- AACAACAAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062767586
seq_region_name: 17
source: dbSNP
start: 73375224
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375225
feature_type: variation
id: rs1353161702
seq_region_name: 17
source: dbSNP
start: 73375225
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062767639
seq_region_name: 17
source: dbSNP
start: 73375226
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1170332081
seq_region_name: 17
source: dbSNP
start: 73375227
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1436119939
seq_region_name: 17
source: dbSNP
start: 73375228
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375229
feature_type: variation
id: rs982376791
seq_region_name: 17
source: dbSNP
start: 73375229
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375230
feature_type: variation
id: rs927815843
seq_region_name: 17
source: dbSNP
start: 73375230
strand: 1
-
alleles:
- CTT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375232
feature_type: variation
id: rs2062767770
seq_region_name: 17
source: dbSNP
start: 73375230
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375233
feature_type: variation
id: rs2062767788
seq_region_name: 17
source: dbSNP
start: 73375230
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145453322
seq_region_name: 17
source: dbSNP
start: 73375230
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375231
feature_type: variation
id: rs1331758720
seq_region_name: 17
source: dbSNP
start: 73375231
strand: 1
-
alleles:
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- TTTTTTTTTTTT
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- TTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375261
feature_type: variation
id: rs33992958
seq_region_name: 17
source: dbSNP
start: 73375231
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375234
feature_type: variation
id: rs2062768054
seq_region_name: 17
source: dbSNP
start: 73375234
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375255
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062768197
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375256
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145453535
seq_region_name: 17
source: dbSNP
start: 73375256
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145453542
seq_region_name: 17
source: dbSNP
start: 73375257
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375260
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375260
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs58092497
seq_region_name: 17
source: dbSNP
start: 73375261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145453589
seq_region_name: 17
source: dbSNP
start: 73375261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1348644663
seq_region_name: 17
source: dbSNP
start: 73375262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062768353
seq_region_name: 17
source: dbSNP
start: 73375262
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062768406
seq_region_name: 17
source: dbSNP
start: 73375263
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375264
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145453631
seq_region_name: 17
source: dbSNP
start: 73375265
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs62072074
seq_region_name: 17
source: dbSNP
start: 73375266
strand: 1
-
alleles:
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- CG
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375267
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375267
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs141736504
seq_region_name: 17
source: dbSNP
start: 73375268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062768660
seq_region_name: 17
source: dbSNP
start: 73375268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1205496709
seq_region_name: 17
source: dbSNP
start: 73375269
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1234339755
seq_region_name: 17
source: dbSNP
start: 73375270
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375274
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375276
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375276
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375279
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062768838
seq_region_name: 17
source: dbSNP
start: 73375280
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs562044041
seq_region_name: 17
source: dbSNP
start: 73375284
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1379663948
seq_region_name: 17
source: dbSNP
start: 73375286
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375287
feature_type: variation
id: rs2062768919
seq_region_name: 17
source: dbSNP
start: 73375287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145453782
seq_region_name: 17
source: dbSNP
start: 73375292
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1335285054
seq_region_name: 17
source: dbSNP
start: 73375296
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375298
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599497328
seq_region_name: 17
source: dbSNP
start: 73375299
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062768980
seq_region_name: 17
source: dbSNP
start: 73375300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1759038400
seq_region_name: 17
source: dbSNP
start: 73375301
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062769006
seq_region_name: 17
source: dbSNP
start: 73375307
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375309
feature_type: variation
id: rs1403571970
seq_region_name: 17
source: dbSNP
start: 73375309
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375310
feature_type: variation
id: rs28718872
seq_region_name: 17
source: dbSNP
start: 73375310
strand: 1
-
alleles:
- GCTCA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375316
feature_type: variation
id: rs373229878
seq_region_name: 17
source: dbSNP
start: 73375312
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375313
feature_type: variation
id: rs1361689999
seq_region_name: 17
source: dbSNP
start: 73375313
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375315
feature_type: variation
id: rs996469602
seq_region_name: 17
source: dbSNP
start: 73375315
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375319
feature_type: variation
id: rs2062769112
seq_region_name: 17
source: dbSNP
start: 73375319
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375322
feature_type: variation
id: rs2062769138
seq_region_name: 17
source: dbSNP
start: 73375322
strand: 1
-
alleles:
- CCCTCACTC
- CCCTCACTCCCTCACTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375330
feature_type: variation
id: rs2062769161
seq_region_name: 17
source: dbSNP
start: 73375322
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375324
feature_type: variation
id: rs2145453915
seq_region_name: 17
source: dbSNP
start: 73375324
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375328
feature_type: variation
id: rs1030237030
seq_region_name: 17
source: dbSNP
start: 73375328
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375330
feature_type: variation
id: rs551035552
seq_region_name: 17
source: dbSNP
start: 73375330
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375331
feature_type: variation
id: rs569271074
seq_region_name: 17
source: dbSNP
start: 73375331
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375334
feature_type: variation
id: rs533291176
seq_region_name: 17
source: dbSNP
start: 73375334
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375342
feature_type: variation
id: rs946381255
seq_region_name: 17
source: dbSNP
start: 73375342
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375343
feature_type: variation
id: rs2062769294
seq_region_name: 17
source: dbSNP
start: 73375342
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375345
feature_type: variation
id: rs1599497377
seq_region_name: 17
source: dbSNP
start: 73375345
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375346
feature_type: variation
id: rs1599497381
seq_region_name: 17
source: dbSNP
start: 73375346
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375347
feature_type: variation
id: rs138899347
seq_region_name: 17
source: dbSNP
start: 73375347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375351
feature_type: variation
id: rs1256783358
seq_region_name: 17
source: dbSNP
start: 73375351
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375353
feature_type: variation
id: rs1202192367
seq_region_name: 17
source: dbSNP
start: 73375353
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375354
feature_type: variation
id: rs1599497399
seq_region_name: 17
source: dbSNP
start: 73375354
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375357
feature_type: variation
id: rs2062769462
seq_region_name: 17
source: dbSNP
start: 73375357
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375359
feature_type: variation
id: rs2062769489
seq_region_name: 17
source: dbSNP
start: 73375359
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375361
feature_type: variation
id: rs1599497407
seq_region_name: 17
source: dbSNP
start: 73375361
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375362
feature_type: variation
id: rs963396417
seq_region_name: 17
source: dbSNP
start: 73375362
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375363
feature_type: variation
id: rs2062769541
seq_region_name: 17
source: dbSNP
start: 73375363
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375365
feature_type: variation
id: rs566723403
seq_region_name: 17
source: dbSNP
start: 73375365
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375366
feature_type: variation
id: rs533767304
seq_region_name: 17
source: dbSNP
start: 73375366
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375367
feature_type: variation
id: rs1313314382
seq_region_name: 17
source: dbSNP
start: 73375367
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375376
feature_type: variation
id: rs1052405704
seq_region_name: 17
source: dbSNP
start: 73375376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375380
feature_type: variation
id: rs948043143
seq_region_name: 17
source: dbSNP
start: 73375380
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375382
feature_type: variation
id: rs1341527499
seq_region_name: 17
source: dbSNP
start: 73375382
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375383
feature_type: variation
id: rs766620230
seq_region_name: 17
source: dbSNP
start: 73375383
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375385
feature_type: variation
id: rs1344419717
seq_region_name: 17
source: dbSNP
start: 73375384
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375387
feature_type: variation
id: rs2062769745
seq_region_name: 17
source: dbSNP
start: 73375387
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375388
feature_type: variation
id: rs762577511
seq_region_name: 17
source: dbSNP
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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- TTGTTGTT
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375453
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062770189
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375461
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73375480
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375484
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375489
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1421085071
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375505
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375510
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375512
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375516
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375517
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1322211936
seq_region_name: 17
source: dbSNP
start: 73375519
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1300455337
seq_region_name: 17
source: dbSNP
start: 73375522
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062770695
seq_region_name: 17
source: dbSNP
start: 73375523
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062770707
seq_region_name: 17
source: dbSNP
start: 73375524
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375526
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375527
feature_type: variation
id: rs1276972065
seq_region_name: 17
source: dbSNP
start: 73375527
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375528
feature_type: variation
id: rs2062770774
seq_region_name: 17
source: dbSNP
start: 73375528
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375530
feature_type: variation
id: rs2062770792
seq_region_name: 17
source: dbSNP
start: 73375530
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062770818
seq_region_name: 17
source: dbSNP
start: 73375534
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145454455
seq_region_name: 17
source: dbSNP
start: 73375536
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375538
feature_type: variation
id: rs890372723
seq_region_name: 17
source: dbSNP
start: 73375538
strand: 1
-
alleles:
- AGCCCAGCCC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375547
feature_type: variation
id: rs1400084660
seq_region_name: 17
source: dbSNP
start: 73375538
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062770884
seq_region_name: 17
source: dbSNP
start: 73375540
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375542
feature_type: variation
id: rs1330595851
seq_region_name: 17
source: dbSNP
start: 73375540
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375541
feature_type: variation
id: rs2062770920
seq_region_name: 17
source: dbSNP
start: 73375541
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1022065310
seq_region_name: 17
source: dbSNP
start: 73375542
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375545
feature_type: variation
id: rs967779338
seq_region_name: 17
source: dbSNP
start: 73375545
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375546
feature_type: variation
id: rs1391241082
seq_region_name: 17
source: dbSNP
start: 73375546
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375548
feature_type: variation
id: rs2145454499
seq_region_name: 17
source: dbSNP
start: 73375548
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375549
feature_type: variation
id: rs1568371219
seq_region_name: 17
source: dbSNP
start: 73375548
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1280317256
seq_region_name: 17
source: dbSNP
start: 73375552
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375554
feature_type: variation
id: rs2062771083
seq_region_name: 17
source: dbSNP
start: 73375554
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375555
feature_type: variation
id: rs1005215855
seq_region_name: 17
source: dbSNP
start: 73375555
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375558
feature_type: variation
id: rs1014672171
seq_region_name: 17
source: dbSNP
start: 73375558
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375559
feature_type: variation
id: rs2145454542
seq_region_name: 17
source: dbSNP
start: 73375559
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145454548
seq_region_name: 17
source: dbSNP
start: 73375569
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375572
feature_type: variation
id: rs2145454554
seq_region_name: 17
source: dbSNP
start: 73375572
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375573
feature_type: variation
id: rs975510367
seq_region_name: 17
source: dbSNP
start: 73375573
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375574
feature_type: variation
id: rs2062771193
seq_region_name: 17
source: dbSNP
start: 73375574
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375575
feature_type: variation
id: rs963202319
seq_region_name: 17
source: dbSNP
start: 73375575
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375576
feature_type: variation
id: rs2062771241
seq_region_name: 17
source: dbSNP
start: 73375576
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375578
feature_type: variation
id: rs2062771273
seq_region_name: 17
source: dbSNP
start: 73375578
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375579
feature_type: variation
id: rs920939206
seq_region_name: 17
source: dbSNP
start: 73375579
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375581
feature_type: variation
id: rs1218248370
seq_region_name: 17
source: dbSNP
start: 73375581
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375583
feature_type: variation
id: rs932262685
seq_region_name: 17
source: dbSNP
start: 73375583
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375584
feature_type: variation
id: rs2062771368
seq_region_name: 17
source: dbSNP
start: 73375584
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375587
feature_type: variation
id: rs2145454628
seq_region_name: 17
source: dbSNP
start: 73375587
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375588
feature_type: variation
id: rs558052477
seq_region_name: 17
source: dbSNP
start: 73375588
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375591
feature_type: variation
id: rs2062771449
seq_region_name: 17
source: dbSNP
start: 73375591
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375592
feature_type: variation
id: rs2062771469
seq_region_name: 17
source: dbSNP
start: 73375592
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375594
feature_type: variation
id: rs1273514284
seq_region_name: 17
source: dbSNP
start: 73375594
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375596
feature_type: variation
id: rs987748728
seq_region_name: 17
source: dbSNP
start: 73375596
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375597
feature_type: variation
id: rs994657984
seq_region_name: 17
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start: 73375597
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-
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73375697
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73375699
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73375718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375720
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375725
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375726
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73375727
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375728
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375729
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375733
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375735
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73375737
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs912160038
seq_region_name: 17
source: dbSNP
start: 73375739
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs940926729
seq_region_name: 17
source: dbSNP
start: 73375740
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375745
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375748
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375749
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375749
strand: 1
-
alleles:
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- GGAGGCTGAGGTGGGAGAATCACTTGAACCTGGGAGGCTGAGGTGGGAGAATCACTTGAACCTGGGAGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375787
feature_type: variation
id: rs1568371315
seq_region_name: 17
source: dbSNP
start: 73375750
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062773099
seq_region_name: 17
source: dbSNP
start: 73375752
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1487710511
seq_region_name: 17
source: dbSNP
start: 73375756
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375759
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1257887432
seq_region_name: 17
source: dbSNP
start: 73375761
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1425905424
seq_region_name: 17
source: dbSNP
start: 73375762
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1185810402
seq_region_name: 17
source: dbSNP
start: 73375764
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062773265
seq_region_name: 17
source: dbSNP
start: 73375765
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062773289
seq_region_name: 17
source: dbSNP
start: 73375766
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375768
feature_type: variation
id: rs972244021
seq_region_name: 17
source: dbSNP
start: 73375768
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375771
feature_type: variation
id: rs1242054138
seq_region_name: 17
source: dbSNP
start: 73375771
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062773339
seq_region_name: 17
source: dbSNP
start: 73375772
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375775
feature_type: variation
id: rs566665514
seq_region_name: 17
source: dbSNP
start: 73375775
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375778
feature_type: variation
id: rs920755409
seq_region_name: 17
source: dbSNP
start: 73375778
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375780
feature_type: variation
id: rs1448843744
seq_region_name: 17
source: dbSNP
start: 73375780
strand: 1
-
alleles:
- GAGGCAGAGGTTGCAGTGAG
- GAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375802
feature_type: variation
id: rs2062773398
seq_region_name: 17
source: dbSNP
start: 73375783
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375787
feature_type: variation
id: rs1035001967
seq_region_name: 17
source: dbSNP
start: 73375787
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375788
feature_type: variation
id: rs527576647
seq_region_name: 17
source: dbSNP
start: 73375788
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375790
feature_type: variation
id: rs2145455269
seq_region_name: 17
source: dbSNP
start: 73375790
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375791
feature_type: variation
id: rs2062773465
seq_region_name: 17
source: dbSNP
start: 73375791
strand: 1
-
alleles:
- TGCAGTGAGCCAAGATCGCACCACTGCA
- TGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375821
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375811
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062773742
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73375821
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375823
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062773905
seq_region_name: 17
source: dbSNP
start: 73375824
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs921442737
seq_region_name: 17
source: dbSNP
start: 73375826
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375827
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375831
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375832
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs760687648
seq_region_name: 17
source: dbSNP
start: 73375832
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375834
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062774089
seq_region_name: 17
source: dbSNP
start: 73375837
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375838
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375838
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375841
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs903695329
seq_region_name: 17
source: dbSNP
start: 73375846
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375850
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375855
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375861
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375863
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375863
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375864
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375865
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73375866
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375867
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1477242181
seq_region_name: 17
source: dbSNP
start: 73375868
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599498013
seq_region_name: 17
source: dbSNP
start: 73375868
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062774584
seq_region_name: 17
source: dbSNP
start: 73375870
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs955272099
seq_region_name: 17
source: dbSNP
start: 73375870
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062774635
seq_region_name: 17
source: dbSNP
start: 73375871
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375872
feature_type: variation
id: rs1007879055
seq_region_name: 17
source: dbSNP
start: 73375872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1440767650
seq_region_name: 17
source: dbSNP
start: 73375872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062774731
seq_region_name: 17
source: dbSNP
start: 73375872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062774757
seq_region_name: 17
source: dbSNP
start: 73375872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375874
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs201971440
seq_region_name: 17
source: dbSNP
start: 73375875
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145455681
seq_region_name: 17
source: dbSNP
start: 73375875
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375876
feature_type: variation
id: rs962302451
seq_region_name: 17
source: dbSNP
start: 73375876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568371410
seq_region_name: 17
source: dbSNP
start: 73375876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73375876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375907
feature_type: variation
id: rs1033602924
seq_region_name: 17
source: dbSNP
start: 73375876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs191364403
seq_region_name: 17
source: dbSNP
start: 73375879
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375880
feature_type: variation
id: rs911533884
seq_region_name: 17
source: dbSNP
start: 73375880
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375881
feature_type: variation
id: rs1318783306
seq_region_name: 17
source: dbSNP
start: 73375881
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375882
feature_type: variation
id: rs1297961784
seq_region_name: 17
source: dbSNP
start: 73375882
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375883
feature_type: variation
id: rs183072893
seq_region_name: 17
source: dbSNP
start: 73375883
strand: 1
-
alleles:
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- TAAACTAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375897
feature_type: variation
id: rs952265179
seq_region_name: 17
source: dbSNP
start: 73375884
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375887
feature_type: variation
id: rs2062775106
seq_region_name: 17
source: dbSNP
start: 73375887
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375888
feature_type: variation
id: rs372091125
seq_region_name: 17
source: dbSNP
start: 73375888
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375888
feature_type: variation
id: rs2062775183
seq_region_name: 17
source: dbSNP
start: 73375889
strand: 1
-
alleles:
- TAAA
- TAAAATAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375892
feature_type: variation
id: rs926755923
seq_region_name: 17
source: dbSNP
start: 73375889
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs899078724
seq_region_name: 17
source: dbSNP
start: 73375891
strand: 1
-
alleles:
- A
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- AATAAAATA
- AATAAAATAAAATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375892
feature_type: variation
id: rs746913907
seq_region_name: 17
source: dbSNP
start: 73375892
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375893
feature_type: variation
id: rs12944777
seq_region_name: 17
source: dbSNP
start: 73375893
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375893
feature_type: variation
id: rs1187315891
seq_region_name: 17
source: dbSNP
start: 73375894
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375896
feature_type: variation
id: rs1423778987
seq_region_name: 17
source: dbSNP
start: 73375896
strand: 1
-
alleles:
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- AATACAATACAATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375900
feature_type: variation
id: rs2062775473
seq_region_name: 17
source: dbSNP
start: 73375897
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375898
feature_type: variation
id: rs1044834472
seq_region_name: 17
source: dbSNP
start: 73375898
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375901
feature_type: variation
id: rs533577013
seq_region_name: 17
source: dbSNP
start: 73375901
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375902
feature_type: variation
id: rs945325155
seq_region_name: 17
source: dbSNP
start: 73375902
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375903
feature_type: variation
id: rs1361000467
seq_region_name: 17
source: dbSNP
start: 73375903
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375906
feature_type: variation
id: rs1599498150
seq_region_name: 17
source: dbSNP
start: 73375906
strand: 1
-
alleles:
- AAAT
- AAATAAAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375909
feature_type: variation
id: rs1599498154
seq_region_name: 17
source: dbSNP
start: 73375906
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375908
feature_type: variation
id: rs905041642
seq_region_name: 17
source: dbSNP
start: 73375908
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375909
feature_type: variation
id: rs2062775763
seq_region_name: 17
source: dbSNP
start: 73375909
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73375913
feature_type: variation
id: rs553686448
seq_region_name: 17
source: dbSNP
start: 73375913
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73376069
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73376074
strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73376078
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73376086
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73376087
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376088
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1476909530
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1319481858
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73376100
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062778406
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062778446
seq_region_name: 17
source: dbSNP
start: 73376106
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs560536396
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1317746332
seq_region_name: 17
source: dbSNP
start: 73376109
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1222909607
seq_region_name: 17
source: dbSNP
start: 73376117
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249033711
seq_region_name: 17
source: dbSNP
start: 73376119
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062778562
seq_region_name: 17
source: dbSNP
start: 73376124
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599498449
seq_region_name: 17
source: dbSNP
start: 73376125
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs368856590
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599498460
seq_region_name: 17
source: dbSNP
start: 73376131
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1275657057
seq_region_name: 17
source: dbSNP
start: 73376132
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778651
seq_region_name: 17
source: dbSNP
start: 73376137
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062778669
seq_region_name: 17
source: dbSNP
start: 73376142
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778691
seq_region_name: 17
source: dbSNP
start: 73376143
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778706
seq_region_name: 17
source: dbSNP
start: 73376144
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1234561498
seq_region_name: 17
source: dbSNP
start: 73376146
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376147
feature_type: variation
id: rs896881304
seq_region_name: 17
source: dbSNP
start: 73376147
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778772
seq_region_name: 17
source: dbSNP
start: 73376148
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1277167456
seq_region_name: 17
source: dbSNP
start: 73376150
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778818
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778843
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778861
seq_region_name: 17
source: dbSNP
start: 73376156
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062778883
seq_region_name: 17
source: dbSNP
start: 73376157
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1430937910
seq_region_name: 17
source: dbSNP
start: 73376159
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1327836311
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1321293665
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs939162207
seq_region_name: 17
source: dbSNP
start: 73376164
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062778985
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1395097944
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1327888437
seq_region_name: 17
source: dbSNP
start: 73376170
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs148823329
seq_region_name: 17
source: dbSNP
start: 73376171
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1423076601
seq_region_name: 17
source: dbSNP
start: 73376172
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1027047929
seq_region_name: 17
source: dbSNP
start: 73376173
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1376160757
seq_region_name: 17
source: dbSNP
start: 73376177
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062779119
seq_region_name: 17
source: dbSNP
start: 73376184
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062779137
seq_region_name: 17
source: dbSNP
start: 73376186
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs549243881
seq_region_name: 17
source: dbSNP
start: 73376187
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1191799204
seq_region_name: 17
source: dbSNP
start: 73376188
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062779207
seq_region_name: 17
source: dbSNP
start: 73376189
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062779228
seq_region_name: 17
source: dbSNP
start: 73376191
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062779246
seq_region_name: 17
source: dbSNP
start: 73376192
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs760856466
seq_region_name: 17
source: dbSNP
start: 73376192
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1197368648
seq_region_name: 17
source: dbSNP
start: 73376192
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs758125106
seq_region_name: 17
source: dbSNP
start: 73376192
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73376193
strand: 1
-
alleles:
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376209
feature_type: variation
id: rs368856491
seq_region_name: 17
source: dbSNP
start: 73376193
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs77558437
seq_region_name: 17
source: dbSNP
start: 73376194
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1422621466
seq_region_name: 17
source: dbSNP
start: 73376195
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062779503
seq_region_name: 17
source: dbSNP
start: 73376197
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1405810682
seq_region_name: 17
source: dbSNP
start: 73376200
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376204
feature_type: variation
id: rs892538166
seq_region_name: 17
source: dbSNP
start: 73376204
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376205
feature_type: variation
id: rs1009662887
seq_region_name: 17
source: dbSNP
start: 73376205
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376207
feature_type: variation
id: rs2145457090
seq_region_name: 17
source: dbSNP
start: 73376207
strand: 1
-
alleles:
- AATTCAAACCTCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376220
feature_type: variation
id: rs2062779596
seq_region_name: 17
source: dbSNP
start: 73376208
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376209
feature_type: variation
id: rs1599498588
seq_region_name: 17
source: dbSNP
start: 73376210
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376210
feature_type: variation
id: rs2062779632
seq_region_name: 17
source: dbSNP
start: 73376210
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376211
feature_type: variation
id: rs2062779654
seq_region_name: 17
source: dbSNP
start: 73376211
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376216
feature_type: variation
id: rs1033902963
seq_region_name: 17
source: dbSNP
start: 73376216
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376218
feature_type: variation
id: rs1444404238
seq_region_name: 17
source: dbSNP
start: 73376218
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376219
feature_type: variation
id: rs2062779732
seq_region_name: 17
source: dbSNP
start: 73376219
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376220
feature_type: variation
id: rs2062779753
seq_region_name: 17
source: dbSNP
start: 73376220
strand: 1
-
alleles:
- CTCATGGACCTGGCTC
- CTCATGGACCTGGCTCATGGACCTGGCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376235
feature_type: variation
id: rs1347993832
seq_region_name: 17
source: dbSNP
start: 73376220
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376221
feature_type: variation
id: rs2062779794
seq_region_name: 17
source: dbSNP
start: 73376221
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376222
feature_type: variation
id: rs1022266343
seq_region_name: 17
source: dbSNP
start: 73376222
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376223
feature_type: variation
id: rs7220670
seq_region_name: 17
source: dbSNP
start: 73376223
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376224
feature_type: variation
id: rs1599498622
seq_region_name: 17
source: dbSNP
start: 73376224
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376229
feature_type: variation
id: rs2062779875
seq_region_name: 17
source: dbSNP
start: 73376229
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376233
feature_type: variation
id: rs1599498630
seq_region_name: 17
source: dbSNP
start: 73376233
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376235
feature_type: variation
id: rs992306139
seq_region_name: 17
source: dbSNP
start: 73376235
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376237
feature_type: variation
id: rs2062779951
seq_region_name: 17
source: dbSNP
start: 73376237
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376239
feature_type: variation
id: rs541301750
seq_region_name: 17
source: dbSNP
start: 73376239
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376245
feature_type: variation
id: rs1028982181
seq_region_name: 17
source: dbSNP
start: 73376245
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376246
feature_type: variation
id: rs955688083
seq_region_name: 17
source: dbSNP
start: 73376246
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376248
feature_type: variation
id: rs2062780033
seq_region_name: 17
source: dbSNP
start: 73376248
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376252
feature_type: variation
id: rs1599498654
seq_region_name: 17
source: dbSNP
start: 73376252
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376256
feature_type: variation
id: rs1397725275
seq_region_name: 17
source: dbSNP
start: 73376256
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376259
feature_type: variation
id: rs1233988187
seq_region_name: 17
source: dbSNP
start: 73376259
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376263
feature_type: variation
id: rs549520227
seq_region_name: 17
source: dbSNP
start: 73376263
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs979482196
seq_region_name: 17
source: dbSNP
start: 73376265
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780216
seq_region_name: 17
source: dbSNP
start: 73376266
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs187276816
seq_region_name: 17
source: dbSNP
start: 73376268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs538335020
seq_region_name: 17
source: dbSNP
start: 73376269
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145457318
seq_region_name: 17
source: dbSNP
start: 73376271
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs747039909
seq_region_name: 17
source: dbSNP
start: 73376274
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780334
seq_region_name: 17
source: dbSNP
start: 73376276
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs971805800
seq_region_name: 17
source: dbSNP
start: 73376283
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599498691
seq_region_name: 17
source: dbSNP
start: 73376285
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780391
seq_region_name: 17
source: dbSNP
start: 73376286
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs547122814
seq_region_name: 17
source: dbSNP
start: 73376288
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs930297983
seq_region_name: 17
source: dbSNP
start: 73376289
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780442
seq_region_name: 17
source: dbSNP
start: 73376292
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780464
seq_region_name: 17
source: dbSNP
start: 73376293
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs980485786
seq_region_name: 17
source: dbSNP
start: 73376294
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780507
seq_region_name: 17
source: dbSNP
start: 73376296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599498706
seq_region_name: 17
source: dbSNP
start: 73376300
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780544
seq_region_name: 17
source: dbSNP
start: 73376301
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565646194
seq_region_name: 17
source: dbSNP
start: 73376303
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs926532114
seq_region_name: 17
source: dbSNP
start: 73376311
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780600
seq_region_name: 17
source: dbSNP
start: 73376312
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs939318112
seq_region_name: 17
source: dbSNP
start: 73376317
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1376037382
seq_region_name: 17
source: dbSNP
start: 73376318
strand: 1
-
alleles:
- "-"
- GAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376319
feature_type: variation
id: rs2062780653
seq_region_name: 17
source: dbSNP
start: 73376320
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1338838470
seq_region_name: 17
source: dbSNP
start: 73376320
strand: 1
-
alleles:
- "-"
- TGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376320
feature_type: variation
id: rs145502599
seq_region_name: 17
source: dbSNP
start: 73376321
strand: 1
-
alleles:
- ACA
- ACATTGTCCCTCCTCACTGCGTTATTCCCAGCTCTGAGAACA
- ACATTGTCCCTGCTCACTGCATTATTCCCAGCTCTGAGAACA
- ACATTGTCCCTGCTCACTGCGTTATTCCCAGCTCTGACAACA
- ACATTGTCCCTGCTCACTGCGTTATTCCCAGCTCTGAGAACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1555754778
seq_region_name: 17
source: dbSNP
start: 73376321
strand: 1
-
alleles:
- ACAATG
- ACAATGTCCCTGCTCACTGCGTTATTCCCAGCTCTGAGAACAATG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568371621
seq_region_name: 17
source: dbSNP
start: 73376321
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1462667867
seq_region_name: 17
source: dbSNP
start: 73376324
strand: 1
-
alleles:
- "-"
- TC
- TCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780806
seq_region_name: 17
source: dbSNP
start: 73376327
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73376328
strand: 1
-
alleles:
- TGGGCACACAATAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145457548
seq_region_name: 17
source: dbSNP
start: 73376328
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73376330
strand: 1
-
alleles:
- GGCACACA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780828
seq_region_name: 17
source: dbSNP
start: 73376330
strand: 1
-
alleles:
- ACACAA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376338
feature_type: variation
id: rs2062780844
seq_region_name: 17
source: dbSNP
start: 73376333
strand: 1
-
alleles:
- ACACAATAAC
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1435499237
seq_region_name: 17
source: dbSNP
start: 73376333
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062780883
seq_region_name: 17
source: dbSNP
start: 73376336
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376338
feature_type: variation
id: rs2062780916
seq_region_name: 17
source: dbSNP
start: 73376338
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062780942
seq_region_name: 17
source: dbSNP
start: 73376340
strand: 1
-
alleles:
- AAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376342
feature_type: variation
id: rs2062780959
seq_region_name: 17
source: dbSNP
start: 73376340
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376342
feature_type: variation
id: rs1377535483
seq_region_name: 17
source: dbSNP
start: 73376342
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs758076830
seq_region_name: 17
source: dbSNP
start: 73376343
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376344
feature_type: variation
id: rs2062781016
seq_region_name: 17
source: dbSNP
start: 73376344
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1419532775
seq_region_name: 17
source: dbSNP
start: 73376345
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376346
feature_type: variation
id: rs534258338
seq_region_name: 17
source: dbSNP
start: 73376346
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376347
feature_type: variation
id: rs556040028
seq_region_name: 17
source: dbSNP
start: 73376347
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376348
feature_type: variation
id: rs2062781146
seq_region_name: 17
source: dbSNP
start: 73376348
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376354
feature_type: variation
id: rs2062781172
seq_region_name: 17
source: dbSNP
start: 73376354
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376356
feature_type: variation
id: rs777215145
seq_region_name: 17
source: dbSNP
start: 73376356
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376357
feature_type: variation
id: rs115356350
seq_region_name: 17
source: dbSNP
start: 73376357
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376359
feature_type: variation
id: rs1036812432
seq_region_name: 17
source: dbSNP
start: 73376359
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376363
feature_type: variation
id: rs1599498781
seq_region_name: 17
source: dbSNP
start: 73376363
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376364
feature_type: variation
id: rs1262816499
seq_region_name: 17
source: dbSNP
start: 73376364
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376366
feature_type: variation
id: rs1214143890
seq_region_name: 17
source: dbSNP
start: 73376366
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376370
feature_type: variation
id: rs2062781337
seq_region_name: 17
source: dbSNP
start: 73376370
strand: 1
-
alleles:
- AAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376376
feature_type: variation
id: rs2062781349
seq_region_name: 17
source: dbSNP
start: 73376374
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376376
feature_type: variation
id: rs2062781386
seq_region_name: 17
source: dbSNP
start: 73376376
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376378
feature_type: variation
id: rs538442790
seq_region_name: 17
source: dbSNP
start: 73376378
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376380
feature_type: variation
id: rs2062781440
seq_region_name: 17
source: dbSNP
start: 73376380
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376382
feature_type: variation
id: rs1225338487
seq_region_name: 17
source: dbSNP
start: 73376382
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376391
feature_type: variation
id: rs2062781487
seq_region_name: 17
source: dbSNP
start: 73376391
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376394
feature_type: variation
id: rs751044564
seq_region_name: 17
source: dbSNP
start: 73376394
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376395
feature_type: variation
id: rs1048094192
seq_region_name: 17
source: dbSNP
start: 73376395
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376400
feature_type: variation
id: rs1411397665
seq_region_name: 17
source: dbSNP
start: 73376400
strand: 1
-
alleles:
- GA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376402
feature_type: variation
id: rs2062781593
seq_region_name: 17
source: dbSNP
start: 73376401
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376404
feature_type: variation
id: rs905535301
seq_region_name: 17
source: dbSNP
start: 73376404
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376405
feature_type: variation
id: rs2062781641
seq_region_name: 17
source: dbSNP
start: 73376405
strand: 1
-
alleles:
- GCCTGC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376412
feature_type: variation
id: rs2062781674
seq_region_name: 17
source: dbSNP
start: 73376407
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376409
feature_type: variation
id: rs1423124398
seq_region_name: 17
source: dbSNP
start: 73376408
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376411
feature_type: variation
id: rs2062781718
seq_region_name: 17
source: dbSNP
start: 73376411
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376415
feature_type: variation
id: rs903969766
seq_region_name: 17
source: dbSNP
start: 73376415
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376416
feature_type: variation
id: rs996833253
seq_region_name: 17
source: dbSNP
start: 73376416
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376422
feature_type: variation
id: rs1361861305
seq_region_name: 17
source: dbSNP
start: 73376422
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376425
feature_type: variation
id: rs192118442
seq_region_name: 17
source: dbSNP
start: 73376425
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376426
feature_type: variation
id: rs2062781851
seq_region_name: 17
source: dbSNP
start: 73376426
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376435
feature_type: variation
id: rs1297185015
seq_region_name: 17
source: dbSNP
start: 73376435
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376437
feature_type: variation
id: rs2062781899
seq_region_name: 17
source: dbSNP
start: 73376437
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376438
feature_type: variation
id: rs1049783817
seq_region_name: 17
source: dbSNP
start: 73376438
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376439
feature_type: variation
id: rs2062781951
seq_region_name: 17
source: dbSNP
start: 73376439
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376441
feature_type: variation
id: rs891336580
seq_region_name: 17
source: dbSNP
start: 73376441
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376445
feature_type: variation
id: rs2062782007
seq_region_name: 17
source: dbSNP
start: 73376445
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376448
feature_type: variation
id: rs2062782030
seq_region_name: 17
source: dbSNP
start: 73376448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376451
feature_type: variation
id: rs1161749119
seq_region_name: 17
source: dbSNP
start: 73376451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376452
feature_type: variation
id: rs1034364881
seq_region_name: 17
source: dbSNP
start: 73376452
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
- C
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376593
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73376594
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73376595
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73376597
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73376601
strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376606
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376608
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73376609
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376610
strand: 1
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alleles:
- TAG
- TAGTTAG
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73376612
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376613
strand: 1
-
alleles:
- GCCTCTGCTGTATTCTGTATGGTGTTGTGCACCTGCACATTTTCCTGGGTCTGTCTATTAACTCACCACTTACAAGCCTC
- GCCTC
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs1568371745
seq_region_name: 17
source: dbSNP
start: 73376613
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73376616
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73376617
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062783561
seq_region_name: 17
source: dbSNP
start: 73376624
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs1013844062
seq_region_name: 17
source: dbSNP
start: 73376625
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1379679541
seq_region_name: 17
source: dbSNP
start: 73376629
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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id: rs1443671073
seq_region_name: 17
source: dbSNP
start: 73376631
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73376632
feature_type: variation
id: rs1398782944
seq_region_name: 17
source: dbSNP
start: 73376632
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1328631290
seq_region_name: 17
source: dbSNP
start: 73376634
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73376638
feature_type: variation
id: rs2062783692
seq_region_name: 17
source: dbSNP
start: 73376638
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs776375707
seq_region_name: 17
source: dbSNP
start: 73376640
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1461088536
seq_region_name: 17
source: dbSNP
start: 73376641
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1874845
seq_region_name: 17
source: dbSNP
start: 73376647
strand: 1
-
alleles:
- TTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062783791
seq_region_name: 17
source: dbSNP
start: 73376652
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1008867594
seq_region_name: 17
source: dbSNP
start: 73376656
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376659
feature_type: variation
id: rs902684619
seq_region_name: 17
source: dbSNP
start: 73376659
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376660
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seq_region_name: 17
source: dbSNP
start: 73376660
strand: 1
-
alleles:
- GGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376662
feature_type: variation
id: rs2062783893
seq_region_name: 17
source: dbSNP
start: 73376660
strand: 1
-
alleles:
- GGTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376663
feature_type: variation
id: rs2062783907
seq_region_name: 17
source: dbSNP
start: 73376660
strand: 1
-
alleles:
- "-"
- CTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376660
feature_type: variation
id: rs1194032209
seq_region_name: 17
source: dbSNP
start: 73376661
strand: 1
-
alleles:
- GTCTGTCT
- GTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376668
feature_type: variation
id: rs2062783955
seq_region_name: 17
source: dbSNP
start: 73376661
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376663
feature_type: variation
id: rs2062783980
seq_region_name: 17
source: dbSNP
start: 73376663
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376664
feature_type: variation
id: rs2062784012
seq_region_name: 17
source: dbSNP
start: 73376664
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376664
feature_type: variation
id: rs2062784047
seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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source: dbSNP
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73376859
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376862
feature_type: variation
id: rs145916000
seq_region_name: 17
source: dbSNP
start: 73376862
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376863
feature_type: variation
id: rs2062786118
seq_region_name: 17
source: dbSNP
start: 73376863
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376868
feature_type: variation
id: rs1037031587
seq_region_name: 17
source: dbSNP
start: 73376868
strand: 1
-
alleles:
- TCCTCCTCCT
- TCCTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376879
feature_type: variation
id: rs1474945644
seq_region_name: 17
source: dbSNP
start: 73376870
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376871
feature_type: variation
id: rs2062786178
seq_region_name: 17
source: dbSNP
start: 73376871
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376872
feature_type: variation
id: rs538537242
seq_region_name: 17
source: dbSNP
start: 73376872
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376876
feature_type: variation
id: rs2062786214
seq_region_name: 17
source: dbSNP
start: 73376876
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376881
feature_type: variation
id: rs897403981
seq_region_name: 17
source: dbSNP
start: 73376881
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376883
feature_type: variation
id: rs902733373
seq_region_name: 17
source: dbSNP
start: 73376883
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376886
feature_type: variation
id: rs2062786289
seq_region_name: 17
source: dbSNP
start: 73376886
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376888
feature_type: variation
id: rs1487437779
seq_region_name: 17
source: dbSNP
start: 73376888
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376890
feature_type: variation
id: rs1261389299
seq_region_name: 17
source: dbSNP
start: 73376890
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376896
feature_type: variation
id: rs931574826
seq_region_name: 17
source: dbSNP
start: 73376896
strand: 1
-
alleles:
- GAGA
- GAGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376899
feature_type: variation
id: rs2145459360
seq_region_name: 17
source: dbSNP
start: 73376896
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376899
feature_type: variation
id: rs1487106760
seq_region_name: 17
source: dbSNP
start: 73376899
strand: 1
-
alleles:
- TT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376904
feature_type: variation
id: rs2062786391
seq_region_name: 17
source: dbSNP
start: 73376903
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376904
feature_type: variation
id: rs1264247470
seq_region_name: 17
source: dbSNP
start: 73376904
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376905
feature_type: variation
id: rs552826385
seq_region_name: 17
source: dbSNP
start: 73376905
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376906
feature_type: variation
id: rs1230889922
seq_region_name: 17
source: dbSNP
start: 73376906
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376908
feature_type: variation
id: rs1331752171
seq_region_name: 17
source: dbSNP
start: 73376908
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376909
feature_type: variation
id: rs1001467970
seq_region_name: 17
source: dbSNP
start: 73376909
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376911
feature_type: variation
id: rs2062786527
seq_region_name: 17
source: dbSNP
start: 73376911
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376919
feature_type: variation
id: rs2062786546
seq_region_name: 17
source: dbSNP
start: 73376919
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376920
feature_type: variation
id: rs1568371888
seq_region_name: 17
source: dbSNP
start: 73376920
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376921
feature_type: variation
id: rs2062786587
seq_region_name: 17
source: dbSNP
start: 73376921
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376922
feature_type: variation
id: rs1053939202
seq_region_name: 17
source: dbSNP
start: 73376922
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376926
feature_type: variation
id: rs763703356
seq_region_name: 17
source: dbSNP
start: 73376926
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376927
feature_type: variation
id: rs1006966699
seq_region_name: 17
source: dbSNP
start: 73376927
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376928
feature_type: variation
id: rs187734311
seq_region_name: 17
source: dbSNP
start: 73376928
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376930
feature_type: variation
id: rs2145459483
seq_region_name: 17
source: dbSNP
start: 73376930
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376934
feature_type: variation
id: rs2062786693
seq_region_name: 17
source: dbSNP
start: 73376934
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376935
feature_type: variation
id: rs2062786723
seq_region_name: 17
source: dbSNP
start: 73376935
strand: 1
-
alleles:
- TGTATTAATG
- TGTATTAATGTATTAATG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376945
feature_type: variation
id: rs2062786742
seq_region_name: 17
source: dbSNP
start: 73376936
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376941
feature_type: variation
id: rs573086067
seq_region_name: 17
source: dbSNP
start: 73376941
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376944
feature_type: variation
id: rs2145459512
seq_region_name: 17
source: dbSNP
start: 73376944
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376947
feature_type: variation
id: rs2062786782
seq_region_name: 17
source: dbSNP
start: 73376947
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376948
feature_type: variation
id: rs2062786799
seq_region_name: 17
source: dbSNP
start: 73376948
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376949
feature_type: variation
id: rs965352842
seq_region_name: 17
source: dbSNP
start: 73376948
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376950
feature_type: variation
id: rs2062786841
seq_region_name: 17
source: dbSNP
start: 73376950
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376956
feature_type: variation
id: rs2062786863
seq_region_name: 17
source: dbSNP
start: 73376956
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376959
feature_type: variation
id: rs777391457
seq_region_name: 17
source: dbSNP
start: 73376959
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376962
feature_type: variation
id: rs2062786891
seq_region_name: 17
source: dbSNP
start: 73376962
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376972
feature_type: variation
id: rs1033425077
seq_region_name: 17
source: dbSNP
start: 73376972
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376974
feature_type: variation
id: rs1323887817
seq_region_name: 17
source: dbSNP
start: 73376974
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376987
feature_type: variation
id: rs2145459575
seq_region_name: 17
source: dbSNP
start: 73376987
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376988
feature_type: variation
id: rs1460975461
seq_region_name: 17
source: dbSNP
start: 73376988
strand: 1
-
alleles:
- CCCACCTGTGGGATGAGGTGCCTTG
- CCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377014
feature_type: variation
id: rs2062786981
seq_region_name: 17
source: dbSNP
start: 73376990
strand: 1
-
alleles:
- CCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTG
- CCCACCTGTGGGATGAGGTGCCTTG
- CCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTG
- CCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377053
feature_type: variation
id: rs1418591323
seq_region_name: 17
source: dbSNP
start: 73376990
strand: 1
-
alleles:
- CCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCAC
- CCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377072
feature_type: variation
id: rs1568371925
seq_region_name: 17
source: dbSNP
start: 73376990
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376994
feature_type: variation
id: rs2062787062
seq_region_name: 17
source: dbSNP
start: 73376994
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73376998
feature_type: variation
id: rs2062787077
seq_region_name: 17
source: dbSNP
start: 73376998
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377000
feature_type: variation
id: rs2062787106
seq_region_name: 17
source: dbSNP
start: 73377000
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377003
feature_type: variation
id: rs2062787129
seq_region_name: 17
source: dbSNP
start: 73377003
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377007
feature_type: variation
id: rs896250750
seq_region_name: 17
source: dbSNP
start: 73377007
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377011
feature_type: variation
id: rs2062787161
seq_region_name: 17
source: dbSNP
start: 73377011
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377012
feature_type: variation
id: rs1476941064
seq_region_name: 17
source: dbSNP
start: 73377012
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377013
feature_type: variation
id: rs138935497
seq_region_name: 17
source: dbSNP
start: 73377013
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377015
feature_type: variation
id: rs371805061
seq_region_name: 17
source: dbSNP
start: 73377015
strand: 1
-
alleles:
- TGTCTCTCCTACTCCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377030
feature_type: variation
id: rs2062787256
seq_region_name: 17
source: dbSNP
start: 73377015
strand: 1
-
alleles:
- GTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCAC
- GTCTCTCCTACTCCCCAC
- GTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377072
feature_type: variation
id: rs1568371942
seq_region_name: 17
source: dbSNP
start: 73377016
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377017
feature_type: variation
id: rs1430701471
seq_region_name: 17
source: dbSNP
start: 73377017
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377026
feature_type: variation
id: rs2062787320
seq_region_name: 17
source: dbSNP
start: 73377026
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377027
feature_type: variation
id: rs2062787341
seq_region_name: 17
source: dbSNP
start: 73377027
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377028
feature_type: variation
id: rs1599499333
seq_region_name: 17
source: dbSNP
start: 73377028
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377029
feature_type: variation
id: rs1265875661
seq_region_name: 17
source: dbSNP
start: 73377029
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377030
feature_type: variation
id: rs2062787413
seq_region_name: 17
source: dbSNP
start: 73377030
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377031
feature_type: variation
id: rs966576696
seq_region_name: 17
source: dbSNP
start: 73377031
strand: 1
-
alleles:
- CCTGTGGGATGAGGTGCCTTGCG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377055
feature_type: variation
id: rs2062787450
seq_region_name: 17
source: dbSNP
start: 73377033
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377036
feature_type: variation
id: rs2062787468
seq_region_name: 17
source: dbSNP
start: 73377036
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377037
feature_type: variation
id: rs1599499348
seq_region_name: 17
source: dbSNP
start: 73377037
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377038
feature_type: variation
id: rs2062787516
seq_region_name: 17
source: dbSNP
start: 73377038
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377040
feature_type: variation
id: rs2062787538
seq_region_name: 17
source: dbSNP
start: 73377038
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377041
feature_type: variation
id: rs201340521
seq_region_name: 17
source: dbSNP
start: 73377041
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377046
feature_type: variation
id: rs2062787587
seq_region_name: 17
source: dbSNP
start: 73377046
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377052
feature_type: variation
id: rs2062787602
seq_region_name: 17
source: dbSNP
start: 73377052
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377054
feature_type: variation
id: rs375092178
seq_region_name: 17
source: dbSNP
start: 73377054
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377055
feature_type: variation
id: rs80251592
seq_region_name: 17
source: dbSNP
start: 73377055
strand: 1
-
alleles:
- GTCTCTCCTACTCCCCAC
- GTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377072
feature_type: variation
id: rs2145459816
seq_region_name: 17
source: dbSNP
start: 73377055
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377056
feature_type: variation
id: rs1273229820
seq_region_name: 17
source: dbSNP
start: 73377056
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377059
feature_type: variation
id: rs2062787705
seq_region_name: 17
source: dbSNP
start: 73377059
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377060
feature_type: variation
id: rs1215049617
seq_region_name: 17
source: dbSNP
start: 73377060
strand: 1
-
alleles:
- CTACT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377066
feature_type: variation
id: rs1337021345
seq_region_name: 17
source: dbSNP
start: 73377062
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377063
feature_type: variation
id: rs2062787753
seq_region_name: 17
source: dbSNP
start: 73377063
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377067
feature_type: variation
id: rs1269272115
seq_region_name: 17
source: dbSNP
start: 73377067
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377068
feature_type: variation
id: rs2145459859
seq_region_name: 17
source: dbSNP
start: 73377068
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377070
feature_type: variation
id: rs1196050993
seq_region_name: 17
source: dbSNP
start: 73377070
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377072
feature_type: variation
id: rs1300997089
seq_region_name: 17
source: dbSNP
start: 73377072
strand: 1
-
alleles:
- C
- CC
- CCTGTGGGATGAGGTGCC
- CCTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCC
- CCTGTGGGCTGAGGTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377072
feature_type: variation
id: rs2062787831
seq_region_name: 17
source: dbSNP
start: 73377072
strand: 1
-
alleles:
- "-"
- CTGTGGGA
- CTGTGGGATGAGG
- CTGTGGGATGAGGTGCCTTG
- CTGTGGGATGAGGTGCCTTGCG
- CTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTG
- CTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATGAGG
- CTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTTGGATGAGGTGCCTTG
- CTGTGGGATGAGGTGCCTTGTG
- CTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTG
- CTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGA
- CTGTGGGATGAGGTGCCTTGTGTCTCTCCTACTCCCCACCTGTGGGATGAGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377072
feature_type: variation
id: rs1568371968
seq_region_name: 17
source: dbSNP
start: 73377073
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377073
feature_type: variation
id: rs952647014
seq_region_name: 17
source: dbSNP
start: 73377073
strand: 1
-
alleles:
- "-"
- GTGGGA
- GTGGGATGAGGTGCCTTGAGTCTCTCCTACTCCCCACCTGAGGCATGTC
- GTGGGATGAGGTGCCTTGTGTCTCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377073
feature_type: variation
id: rs1599499386
seq_region_name: 17
source: dbSNP
start: 73377074
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377074
feature_type: variation
id: rs1599499390
seq_region_name: 17
source: dbSNP
start: 73377074
strand: 1
-
alleles:
- "-"
- GTGGG
- GTGTCTCTCCTACTCCCCACCTGTGGG
- GTGTCTCTCCTACTCCCCACCTGTGGGATG
- GTGTCTCTCCTACTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377074
feature_type: variation
id: rs2062788002
seq_region_name: 17
source: dbSNP
start: 73377075
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377075
feature_type: variation
id: rs1267599055
seq_region_name: 17
source: dbSNP
start: 73377075
strand: 1
-
alleles:
- "-"
- CTCCCC
- CTCCCCACCTGTGGGATG
- CTCCCCACCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGTGGGATG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377075
feature_type: variation
id: rs2062788067
seq_region_name: 17
source: dbSNP
start: 73377076
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377076
feature_type: variation
id: rs1477916570
seq_region_name: 17
source: dbSNP
start: 73377076
strand: 1
-
alleles:
- "-"
- CCTGTGGGATGAGGT
- CCTGTGGGATGAGGTGCCTTGCGTCTCTCCTACTCCCCACCTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377076
feature_type: variation
id: rs2145459964
seq_region_name: 17
source: dbSNP
start: 73377077
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377077
feature_type: variation
id: rs767064167
seq_region_name: 17
source: dbSNP
start: 73377077
strand: 1
-
alleles:
- G
- GTGCCTTGCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377077
feature_type: variation
id: rs2062788141
seq_region_name: 17
source: dbSNP
start: 73377077
strand: 1
-
alleles:
- "-"
- GGATGAGGTGCCTTGTGTCTCTCCTACTCCCCA
- GTGACTTGCGTCTCTCCTACTCC
- GTGCCTTGCGTCTCTCCTACTCC
- GTGCCTTGTGTCTCTCCTACTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377077
feature_type: variation
id: rs2062788173
seq_region_name: 17
source: dbSNP
start: 73377078
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377078
feature_type: variation
id: rs2062788204
seq_region_name: 17
source: dbSNP
start: 73377078
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377079
feature_type: variation
id: rs2062788227
seq_region_name: 17
source: dbSNP
start: 73377079
strand: 1
-
alleles:
- "-"
- TTGCGTCTCTCCTACTCCCCACCTGTGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377079
feature_type: variation
id: rs2145460002
seq_region_name: 17
source: dbSNP
start: 73377080
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377080
feature_type: variation
id: rs1195464226
seq_region_name: 17
source: dbSNP
start: 73377080
strand: 1
-
alleles:
- "-"
- CCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377080
feature_type: variation
id: rs2145460013
seq_region_name: 17
source: dbSNP
start: 73377081
strand: 1
-
alleles:
- "-"
- GATGAGGTGCCTTGCGTCTCTCCTACTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377083
feature_type: variation
id: rs2145460020
seq_region_name: 17
source: dbSNP
start: 73377084
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377086
feature_type: variation
id: rs2145460027
seq_region_name: 17
source: dbSNP
start: 73377086
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377087
feature_type: variation
id: rs1408323978
seq_region_name: 17
source: dbSNP
start: 73377087
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377089
feature_type: variation
id: rs2062788278
seq_region_name: 17
source: dbSNP
start: 73377089
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377093
feature_type: variation
id: rs984386859
seq_region_name: 17
source: dbSNP
start: 73377093
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377097
feature_type: variation
id: rs2062788327
seq_region_name: 17
source: dbSNP
start: 73377097
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377099
feature_type: variation
id: rs2062788346
seq_region_name: 17
source: dbSNP
start: 73377099
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377100
feature_type: variation
id: rs1426190698
seq_region_name: 17
source: dbSNP
start: 73377100
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377102
feature_type: variation
id: rs1168777502
seq_region_name: 17
source: dbSNP
start: 73377102
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377104
feature_type: variation
id: rs1476584887
seq_region_name: 17
source: dbSNP
start: 73377104
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377108
feature_type: variation
id: rs2062788464
seq_region_name: 17
source: dbSNP
start: 73377108
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377110
feature_type: variation
id: rs1599499419
seq_region_name: 17
source: dbSNP
start: 73377110
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377111
feature_type: variation
id: rs991969318
seq_region_name: 17
source: dbSNP
start: 73377111
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377112
feature_type: variation
id: rs199555255
seq_region_name: 17
source: dbSNP
start: 73377112
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377113
feature_type: variation
id: rs1393590315
seq_region_name: 17
source: dbSNP
start: 73377113
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377116
feature_type: variation
id: rs142842884
seq_region_name: 17
source: dbSNP
start: 73377116
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377117
feature_type: variation
id: rs912644410
seq_region_name: 17
source: dbSNP
start: 73377117
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377118
feature_type: variation
id: rs1194927102
seq_region_name: 17
source: dbSNP
start: 73377118
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377119
feature_type: variation
id: rs2062788616
seq_region_name: 17
source: dbSNP
start: 73377119
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377122
feature_type: variation
id: rs2062788640
seq_region_name: 17
source: dbSNP
start: 73377122
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377125
feature_type: variation
id: rs1392007815
seq_region_name: 17
source: dbSNP
start: 73377125
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377126
feature_type: variation
id: rs750824292
seq_region_name: 17
source: dbSNP
start: 73377126
strand: 1
-
alleles:
- GAGAG
- GAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377130
feature_type: variation
id: rs1195963231
seq_region_name: 17
source: dbSNP
start: 73377126
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377128
feature_type: variation
id: rs572405233
seq_region_name: 17
source: dbSNP
start: 73377128
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377131
feature_type: variation
id: rs2062788733
seq_region_name: 17
source: dbSNP
start: 73377131
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377132
feature_type: variation
id: rs1277873597
seq_region_name: 17
source: dbSNP
start: 73377132
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377134
feature_type: variation
id: rs2062788781
seq_region_name: 17
source: dbSNP
start: 73377134
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377136
feature_type: variation
id: rs192699875
seq_region_name: 17
source: dbSNP
start: 73377136
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377144
feature_type: variation
id: rs2062788835
seq_region_name: 17
source: dbSNP
start: 73377144
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377146
feature_type: variation
id: rs2062788866
seq_region_name: 17
source: dbSNP
start: 73377146
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377148
feature_type: variation
id: rs1321626796
seq_region_name: 17
source: dbSNP
start: 73377148
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377149
feature_type: variation
id: rs373535577
seq_region_name: 17
source: dbSNP
start: 73377149
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377153
feature_type: variation
id: rs2062788926
seq_region_name: 17
source: dbSNP
start: 73377153
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377155
feature_type: variation
id: rs1440103291
seq_region_name: 17
source: dbSNP
start: 73377155
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377159
feature_type: variation
id: rs916977687
seq_region_name: 17
source: dbSNP
start: 73377159
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377161
feature_type: variation
id: rs1329634866
seq_region_name: 17
source: dbSNP
start: 73377161
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377163
feature_type: variation
id: rs1344988618
seq_region_name: 17
source: dbSNP
start: 73377163
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377168
feature_type: variation
id: rs2062789002
seq_region_name: 17
source: dbSNP
start: 73377168
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377169
feature_type: variation
id: rs1373896218
seq_region_name: 17
source: dbSNP
start: 73377169
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377172
feature_type: variation
id: rs796506958
seq_region_name: 17
source: dbSNP
start: 73377172
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377173
feature_type: variation
id: rs2062789070
seq_region_name: 17
source: dbSNP
start: 73377173
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377174
feature_type: variation
id: rs1397426203
seq_region_name: 17
source: dbSNP
start: 73377174
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377178
feature_type: variation
id: rs200669326
seq_region_name: 17
source: dbSNP
start: 73377174
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377175
feature_type: variation
id: rs1157398327
seq_region_name: 17
source: dbSNP
start: 73377175
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377176
feature_type: variation
id: rs1338137412
seq_region_name: 17
source: dbSNP
start: 73377176
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377180
feature_type: variation
id: rs1796171742
seq_region_name: 17
source: dbSNP
start: 73377180
strand: 1
-
alleles:
- CCAACCA
- CCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377195
feature_type: variation
id: rs1226351585
seq_region_name: 17
source: dbSNP
start: 73377189
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377190
feature_type: variation
id: rs1265819903
seq_region_name: 17
source: dbSNP
start: 73377190
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377202
feature_type: variation
id: rs574716630
seq_region_name: 17
source: dbSNP
start: 73377202
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377203
feature_type: variation
id: rs1599499503
seq_region_name: 17
source: dbSNP
start: 73377203
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377205
feature_type: variation
id: rs2062789239
seq_region_name: 17
source: dbSNP
start: 73377205
strand: 1
-
alleles:
- TTCCTTTTTTTTTTTTC
- TTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377222
feature_type: variation
id: rs1208016846
seq_region_name: 17
source: dbSNP
start: 73377206
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377207
feature_type: variation
id: rs371624539
seq_region_name: 17
source: dbSNP
start: 73377207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377208
feature_type: variation
id: rs1599499519
seq_region_name: 17
source: dbSNP
start: 73377208
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377209
feature_type: variation
id: rs201678481
seq_region_name: 17
source: dbSNP
start: 73377208
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377209
feature_type: variation
id: rs917780511
seq_region_name: 17
source: dbSNP
start: 73377209
strand: 1
-
alleles:
- CTTT
- "-"
assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73377229
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73377230
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73377232
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1158617384
seq_region_name: 17
source: dbSNP
start: 73377233
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377236
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377238
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377240
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377242
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377243
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377247
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377250
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377251
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73377253
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377255
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377258
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73377259
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377260
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377268
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377271
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73377274
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062790406
seq_region_name: 17
source: dbSNP
start: 73377275
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377280
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1292763412
seq_region_name: 17
source: dbSNP
start: 73377281
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1358790255
seq_region_name: 17
source: dbSNP
start: 73377282
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062790510
seq_region_name: 17
source: dbSNP
start: 73377289
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377293
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377298
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599499651
seq_region_name: 17
source: dbSNP
start: 73377299
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377300
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs942833450
seq_region_name: 17
source: dbSNP
start: 73377301
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1346275630
seq_region_name: 17
source: dbSNP
start: 73377304
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377305
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs896230728
seq_region_name: 17
source: dbSNP
start: 73377309
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs901237891
seq_region_name: 17
source: dbSNP
start: 73377311
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377313
feature_type: variation
id: rs2062790755
seq_region_name: 17
source: dbSNP
start: 73377313
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377314
feature_type: variation
id: rs2062790776
seq_region_name: 17
source: dbSNP
start: 73377314
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377318
feature_type: variation
id: rs1475304619
seq_region_name: 17
source: dbSNP
start: 73377318
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs532348652
seq_region_name: 17
source: dbSNP
start: 73377321
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377322
feature_type: variation
id: rs1020607629
seq_region_name: 17
source: dbSNP
start: 73377322
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs888403236
seq_region_name: 17
source: dbSNP
start: 73377324
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377325
feature_type: variation
id: rs2062790892
seq_region_name: 17
source: dbSNP
start: 73377325
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1210451665
seq_region_name: 17
source: dbSNP
start: 73377327
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062790936
seq_region_name: 17
source: dbSNP
start: 73377330
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1005460809
seq_region_name: 17
source: dbSNP
start: 73377334
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062790975
seq_region_name: 17
source: dbSNP
start: 73377337
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377342
feature_type: variation
id: rs879921963
seq_region_name: 17
source: dbSNP
start: 73377342
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377343
feature_type: variation
id: rs2062791026
seq_region_name: 17
source: dbSNP
start: 73377343
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377344
feature_type: variation
id: rs1034648891
seq_region_name: 17
source: dbSNP
start: 73377344
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377345
feature_type: variation
id: rs1599499701
seq_region_name: 17
source: dbSNP
start: 73377345
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377346
feature_type: variation
id: rs1314378434
seq_region_name: 17
source: dbSNP
start: 73377346
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377347
feature_type: variation
id: rs1214346081
seq_region_name: 17
source: dbSNP
start: 73377347
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377348
feature_type: variation
id: rs1870370647
seq_region_name: 17
source: dbSNP
start: 73377348
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377353
feature_type: variation
id: rs902192163
seq_region_name: 17
source: dbSNP
start: 73377353
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377354
feature_type: variation
id: rs1272299745
seq_region_name: 17
source: dbSNP
start: 73377354
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377357
feature_type: variation
id: rs1439254913
seq_region_name: 17
source: dbSNP
start: 73377357
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062791231
seq_region_name: 17
source: dbSNP
start: 73377362
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377364
feature_type: variation
id: rs1599499716
seq_region_name: 17
source: dbSNP
start: 73377364
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377365
feature_type: variation
id: rs1353783524
seq_region_name: 17
source: dbSNP
start: 73377365
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377366
feature_type: variation
id: rs1241609433
seq_region_name: 17
source: dbSNP
start: 73377366
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377367
feature_type: variation
id: rs1000560181
seq_region_name: 17
source: dbSNP
start: 73377367
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377368
feature_type: variation
id: rs1032241578
seq_region_name: 17
source: dbSNP
start: 73377368
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377369
feature_type: variation
id: rs954138247
seq_region_name: 17
source: dbSNP
start: 73377369
strand: 1
-
alleles:
- ACCACGCCTGGATAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGATCTCCTGACC
- ACC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377450
feature_type: variation
id: rs2062791416
seq_region_name: 17
source: dbSNP
start: 73377371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1257271829
seq_region_name: 17
source: dbSNP
start: 73377373
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs373748021
seq_region_name: 17
source: dbSNP
start: 73377375
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1444532074
seq_region_name: 17
source: dbSNP
start: 73377376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1019873119
seq_region_name: 17
source: dbSNP
start: 73377377
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377379
feature_type: variation
id: rs1182276997
seq_region_name: 17
source: dbSNP
start: 73377379
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377382
feature_type: variation
id: rs1385217063
seq_region_name: 17
source: dbSNP
start: 73377382
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377383
feature_type: variation
id: rs2062791541
seq_region_name: 17
source: dbSNP
start: 73377383
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377384
feature_type: variation
id: rs2062791574
seq_region_name: 17
source: dbSNP
start: 73377384
strand: 1
-
alleles:
- TTTTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377390
feature_type: variation
id: rs1440854745
seq_region_name: 17
source: dbSNP
start: 73377386
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377391
feature_type: variation
id: rs1252350799
seq_region_name: 17
source: dbSNP
start: 73377391
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377391
feature_type: variation
id: rs2062791620
seq_region_name: 17
source: dbSNP
start: 73377391
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377394
feature_type: variation
id: rs965453130
seq_region_name: 17
source: dbSNP
start: 73377394
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377398
feature_type: variation
id: rs1489544659
seq_region_name: 17
source: dbSNP
start: 73377398
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377405
feature_type: variation
id: rs2062791716
seq_region_name: 17
source: dbSNP
start: 73377405
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377406
feature_type: variation
id: rs1249819357
seq_region_name: 17
source: dbSNP
start: 73377406
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377407
feature_type: variation
id: rs28412293
seq_region_name: 17
source: dbSNP
start: 73377407
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377408
feature_type: variation
id: rs2062791761
seq_region_name: 17
source: dbSNP
start: 73377408
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377410
feature_type: variation
id: rs541639135
seq_region_name: 17
source: dbSNP
start: 73377410
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377413
feature_type: variation
id: rs1232623393
seq_region_name: 17
source: dbSNP
start: 73377413
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377420
feature_type: variation
id: rs1370870223
seq_region_name: 17
source: dbSNP
start: 73377420
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377429
feature_type: variation
id: rs2062791849
seq_region_name: 17
source: dbSNP
start: 73377429
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377431
feature_type: variation
id: rs2145461054
seq_region_name: 17
source: dbSNP
start: 73377431
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377434
feature_type: variation
id: rs1453300344
seq_region_name: 17
source: dbSNP
start: 73377434
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377436
feature_type: variation
id: rs1304899920
seq_region_name: 17
source: dbSNP
start: 73377436
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377437
feature_type: variation
id: rs918558208
seq_region_name: 17
source: dbSNP
start: 73377437
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377438
feature_type: variation
id: rs529713708
seq_region_name: 17
source: dbSNP
start: 73377438
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377439
feature_type: variation
id: rs1404082299
seq_region_name: 17
source: dbSNP
start: 73377439
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377441
feature_type: variation
id: rs1394132609
seq_region_name: 17
source: dbSNP
start: 73377441
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377442
feature_type: variation
id: rs1170223663
seq_region_name: 17
source: dbSNP
start: 73377442
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377446
feature_type: variation
id: rs1432672287
seq_region_name: 17
source: dbSNP
start: 73377446
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377447
feature_type: variation
id: rs2062792106
seq_region_name: 17
source: dbSNP
start: 73377447
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377452
feature_type: variation
id: rs2062792130
seq_region_name: 17
source: dbSNP
start: 73377452
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377454
feature_type: variation
id: rs1599499821
seq_region_name: 17
source: dbSNP
start: 73377454
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377455
feature_type: variation
id: rs967099629
seq_region_name: 17
source: dbSNP
start: 73377455
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377457
feature_type: variation
id: rs1174249342
seq_region_name: 17
source: dbSNP
start: 73377457
strand: 1
-
alleles:
- G
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377457
feature_type: variation
id: rs2062792225
seq_region_name: 17
source: dbSNP
start: 73377457
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377462
feature_type: variation
id: rs2145461173
seq_region_name: 17
source: dbSNP
start: 73377461
strand: 1
-
alleles:
- "-"
- GC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377463
feature_type: variation
id: rs2145461185
seq_region_name: 17
source: dbSNP
start: 73377464
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377465
feature_type: variation
id: rs2145461192
seq_region_name: 17
source: dbSNP
start: 73377465
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377466
feature_type: variation
id: rs2062792248
seq_region_name: 17
source: dbSNP
start: 73377466
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377467
feature_type: variation
id: rs2062792277
seq_region_name: 17
source: dbSNP
start: 73377467
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377468
feature_type: variation
id: rs1434848663
seq_region_name: 17
source: dbSNP
start: 73377468
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377470
feature_type: variation
id: rs2062792328
seq_region_name: 17
source: dbSNP
start: 73377470
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377471
feature_type: variation
id: rs977124635
seq_region_name: 17
source: dbSNP
start: 73377471
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377473
feature_type: variation
id: rs28698457
seq_region_name: 17
source: dbSNP
start: 73377473
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377475
feature_type: variation
id: rs2062792421
seq_region_name: 17
source: dbSNP
start: 73377475
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377482
feature_type: variation
id: rs1481052908
seq_region_name: 17
source: dbSNP
start: 73377482
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377485
feature_type: variation
id: rs2145461265
seq_region_name: 17
source: dbSNP
start: 73377485
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377486
feature_type: variation
id: rs1242265543
seq_region_name: 17
source: dbSNP
start: 73377486
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377487
feature_type: variation
id: rs1209176266
seq_region_name: 17
source: dbSNP
start: 73377487
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377492
feature_type: variation
id: rs1347690947
seq_region_name: 17
source: dbSNP
start: 73377492
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377495
feature_type: variation
id: rs2062792532
seq_region_name: 17
source: dbSNP
start: 73377495
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377496
feature_type: variation
id: rs1281515930
seq_region_name: 17
source: dbSNP
start: 73377496
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377501
feature_type: variation
id: rs927568521
seq_region_name: 17
source: dbSNP
start: 73377501
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377502
feature_type: variation
id: rs867288188
seq_region_name: 17
source: dbSNP
start: 73377502
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377510
feature_type: variation
id: rs2062792640
seq_region_name: 17
source: dbSNP
start: 73377510
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377511
feature_type: variation
id: rs1304175262
seq_region_name: 17
source: dbSNP
start: 73377511
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377512
feature_type: variation
id: rs749643024
seq_region_name: 17
source: dbSNP
start: 73377512
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377514
feature_type: variation
id: rs2062792727
seq_region_name: 17
source: dbSNP
start: 73377514
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377517
feature_type: variation
id: rs1350692162
seq_region_name: 17
source: dbSNP
start: 73377517
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377518
feature_type: variation
id: rs2062792766
seq_region_name: 17
source: dbSNP
start: 73377518
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377521
feature_type: variation
id: rs2062792795
seq_region_name: 17
source: dbSNP
start: 73377521
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377522
feature_type: variation
id: rs1309540358
seq_region_name: 17
source: dbSNP
start: 73377522
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377525
feature_type: variation
id: rs149346847
seq_region_name: 17
source: dbSNP
start: 73377525
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377527
feature_type: variation
id: rs1568372211
seq_region_name: 17
source: dbSNP
start: 73377527
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377536
feature_type: variation
id: rs549643399
seq_region_name: 17
source: dbSNP
start: 73377536
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377538
feature_type: variation
id: rs2062792894
seq_region_name: 17
source: dbSNP
start: 73377538
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377542
feature_type: variation
id: rs2062792918
seq_region_name: 17
source: dbSNP
start: 73377542
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377543
feature_type: variation
id: rs1202100592
seq_region_name: 17
source: dbSNP
start: 73377543
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377547
feature_type: variation
id: rs2062792979
seq_region_name: 17
source: dbSNP
start: 73377547
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377549
feature_type: variation
id: rs949085620
seq_region_name: 17
source: dbSNP
start: 73377549
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377555
feature_type: variation
id: rs1042145496
seq_region_name: 17
source: dbSNP
start: 73377555
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377558
feature_type: variation
id: rs2062793080
seq_region_name: 17
source: dbSNP
start: 73377558
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377559
feature_type: variation
id: rs2062793109
seq_region_name: 17
source: dbSNP
start: 73377559
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377562
feature_type: variation
id: rs1458571610
seq_region_name: 17
source: dbSNP
start: 73377562
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377565
feature_type: variation
id: rs532078363
seq_region_name: 17
source: dbSNP
start: 73377565
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377569
feature_type: variation
id: rs369591782
seq_region_name: 17
source: dbSNP
start: 73377569
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377574
feature_type: variation
id: rs1158439311
seq_region_name: 17
source: dbSNP
start: 73377574
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377580
feature_type: variation
id: rs941359353
seq_region_name: 17
source: dbSNP
start: 73377580
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377581
feature_type: variation
id: rs2062793243
seq_region_name: 17
source: dbSNP
start: 73377581
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377582
feature_type: variation
id: rs2062793270
seq_region_name: 17
source: dbSNP
start: 73377582
strand: 1
-
alleles:
- CCTCGG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377588
feature_type: variation
id: rs2062793291
seq_region_name: 17
source: dbSNP
start: 73377583
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377584
feature_type: variation
id: rs2145461522
seq_region_name: 17
source: dbSNP
start: 73377584
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377586
feature_type: variation
id: rs902286818
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377697
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73377699
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73377700
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377701
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377707
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377721
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377722
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062794852
seq_region_name: 17
source: dbSNP
start: 73377726
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377728
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377730
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73377732
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs965197262
seq_region_name: 17
source: dbSNP
start: 73377737
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377738
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062795000
seq_region_name: 17
source: dbSNP
start: 73377739
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377740
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062795043
seq_region_name: 17
source: dbSNP
start: 73377741
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377746
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377751
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377753
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377754
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062795156
seq_region_name: 17
source: dbSNP
start: 73377759
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs369834410
seq_region_name: 17
source: dbSNP
start: 73377761
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377762
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377762
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73377764
feature_type: variation
id: rs577016287
seq_region_name: 17
source: dbSNP
start: 73377764
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73377905
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73377910
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377920
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377922
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377924
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73377927
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377928
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73377932
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73378132
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378134
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73378138
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73378160
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378162
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378163
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378164
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378165
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378166
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378169
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378170
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378175
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378180
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378183
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378188
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378189
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378190
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378192
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378192
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599500582
seq_region_name: 17
source: dbSNP
start: 73378198
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062799504
seq_region_name: 17
source: dbSNP
start: 73378200
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1017275874
seq_region_name: 17
source: dbSNP
start: 73378204
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73378210
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73378365
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73378368
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73378371
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73378371
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378372
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378373
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378387
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378387
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378388
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378389
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378396
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062801499
seq_region_name: 17
source: dbSNP
start: 73378398
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378400
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs892969114
seq_region_name: 17
source: dbSNP
start: 73378404
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73378405
feature_type: variation
id: rs2062801573
seq_region_name: 17
source: dbSNP
start: 73378405
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73378406
feature_type: variation
id: rs2062801596
seq_region_name: 17
source: dbSNP
start: 73378406
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73378528
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378529
strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378533
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378535
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378538
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378539
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378540
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378544
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378545
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73378546
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378547
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378555
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73378557
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378562
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73378565
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73378568
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378570
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73378571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145464569
seq_region_name: 17
source: dbSNP
start: 73378573
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062803558
seq_region_name: 17
source: dbSNP
start: 73378574
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1435746575
seq_region_name: 17
source: dbSNP
start: 73378576
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378577
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1321709030
seq_region_name: 17
source: dbSNP
start: 73378578
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73378579
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1440040943
seq_region_name: 17
source: dbSNP
start: 73378580
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378581
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378591
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378592
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378601
strand: 1
-
alleles:
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- GATGGGATGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062803818
seq_region_name: 17
source: dbSNP
start: 73378606
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378608
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378609
strand: 1
-
alleles:
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- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73378612
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id: rs1368526327
seq_region_name: 17
source: dbSNP
start: 73378609
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73378610
feature_type: variation
id: rs1196159051
seq_region_name: 17
source: dbSNP
start: 73378610
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378968
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73378971
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378979
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378984
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378987
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73378988
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378990
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73378998
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73378999
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs909551187
seq_region_name: 17
source: dbSNP
start: 73379000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1246418627
seq_region_name: 17
source: dbSNP
start: 73379001
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73379010
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379014
feature_type: variation
id: rs1222750224
seq_region_name: 17
source: dbSNP
start: 73379014
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379015
feature_type: variation
id: rs962923790
seq_region_name: 17
source: dbSNP
start: 73379015
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379019
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1272935644
seq_region_name: 17
source: dbSNP
start: 73379021
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379022
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062808142
seq_region_name: 17
source: dbSNP
start: 73379028
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1044634749
seq_region_name: 17
source: dbSNP
start: 73379034
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379035
feature_type: variation
id: rs2062808178
seq_region_name: 17
source: dbSNP
start: 73379034
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379035
feature_type: variation
id: rs1343524412
seq_region_name: 17
source: dbSNP
start: 73379035
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379036
feature_type: variation
id: rs73345936
seq_region_name: 17
source: dbSNP
start: 73379036
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379039
feature_type: variation
id: rs915843225
seq_region_name: 17
source: dbSNP
start: 73379039
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs760010788
seq_region_name: 17
source: dbSNP
start: 73379042
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs552408220
seq_region_name: 17
source: dbSNP
start: 73379052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs956138459
seq_region_name: 17
source: dbSNP
start: 73379053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379056
feature_type: variation
id: rs2062808322
seq_region_name: 17
source: dbSNP
start: 73379056
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379059
feature_type: variation
id: rs1568372874
seq_region_name: 17
source: dbSNP
start: 73379059
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379060
feature_type: variation
id: rs2062808376
seq_region_name: 17
source: dbSNP
start: 73379060
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379061
feature_type: variation
id: rs1436757974
seq_region_name: 17
source: dbSNP
start: 73379061
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379062
feature_type: variation
id: rs1432028906
seq_region_name: 17
source: dbSNP
start: 73379062
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379063
feature_type: variation
id: rs2062808449
seq_region_name: 17
source: dbSNP
start: 73379063
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379066
feature_type: variation
id: rs1488386209
seq_region_name: 17
source: dbSNP
start: 73379065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379073
feature_type: variation
id: rs1599501427
seq_region_name: 17
source: dbSNP
start: 73379073
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379074
feature_type: variation
id: rs1045633584
seq_region_name: 17
source: dbSNP
start: 73379074
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379076
feature_type: variation
id: rs2062808539
seq_region_name: 17
source: dbSNP
start: 73379076
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379077
feature_type: variation
id: rs1206580611
seq_region_name: 17
source: dbSNP
start: 73379077
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379078
feature_type: variation
id: rs2062808585
seq_region_name: 17
source: dbSNP
start: 73379078
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379080
feature_type: variation
id: rs570897164
seq_region_name: 17
source: dbSNP
start: 73379080
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379084
feature_type: variation
id: rs2062808626
seq_region_name: 17
source: dbSNP
start: 73379084
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379086
feature_type: variation
id: rs924682826
seq_region_name: 17
source: dbSNP
start: 73379086
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379087
feature_type: variation
id: rs2145465984
seq_region_name: 17
source: dbSNP
start: 73379087
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379089
feature_type: variation
id: rs1264267617
seq_region_name: 17
source: dbSNP
start: 73379089
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379091
feature_type: variation
id: rs1012027764
seq_region_name: 17
source: dbSNP
start: 73379091
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379095
feature_type: variation
id: rs1021616959
seq_region_name: 17
source: dbSNP
start: 73379095
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379096
feature_type: variation
id: rs775390155
seq_region_name: 17
source: dbSNP
start: 73379096
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379097
feature_type: variation
id: rs2062808754
seq_region_name: 17
source: dbSNP
start: 73379097
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379098
feature_type: variation
id: rs2062808773
seq_region_name: 17
source: dbSNP
start: 73379098
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379099
feature_type: variation
id: rs2062808796
seq_region_name: 17
source: dbSNP
start: 73379099
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379103
feature_type: variation
id: rs2062808811
seq_region_name: 17
source: dbSNP
start: 73379103
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379104
feature_type: variation
id: rs2062808834
seq_region_name: 17
source: dbSNP
start: 73379104
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379105
feature_type: variation
id: rs1424561749
seq_region_name: 17
source: dbSNP
start: 73379105
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379108
feature_type: variation
id: rs2145466057
seq_region_name: 17
source: dbSNP
start: 73379108
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379115
feature_type: variation
id: rs1191919247
seq_region_name: 17
source: dbSNP
start: 73379115
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379117
feature_type: variation
id: rs1481558274
seq_region_name: 17
source: dbSNP
start: 73379117
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379121
feature_type: variation
id: rs1250001663
seq_region_name: 17
source: dbSNP
start: 73379121
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379124
feature_type: variation
id: rs867252722
seq_region_name: 17
source: dbSNP
start: 73379124
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379125
feature_type: variation
id: rs1193083568
seq_region_name: 17
source: dbSNP
start: 73379125
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379126
feature_type: variation
id: rs1244227603
seq_region_name: 17
source: dbSNP
start: 73379126
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379129
feature_type: variation
id: rs2145466106
seq_region_name: 17
source: dbSNP
start: 73379129
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379130
feature_type: variation
id: rs2145466114
seq_region_name: 17
source: dbSNP
start: 73379130
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379133
feature_type: variation
id: rs534711935
seq_region_name: 17
source: dbSNP
start: 73379133
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379140
feature_type: variation
id: rs772928262
seq_region_name: 17
source: dbSNP
start: 73379140
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379141
feature_type: variation
id: rs1202453470
seq_region_name: 17
source: dbSNP
start: 73379141
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379142
feature_type: variation
id: rs749234329
seq_region_name: 17
source: dbSNP
start: 73379142
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379143
feature_type: variation
id: rs762604112
seq_region_name: 17
source: dbSNP
start: 73379143
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379149
feature_type: variation
id: rs1205506743
seq_region_name: 17
source: dbSNP
start: 73379149
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379150
feature_type: variation
id: rs367948638
seq_region_name: 17
source: dbSNP
start: 73379150
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379160
feature_type: variation
id: rs370403996
seq_region_name: 17
source: dbSNP
start: 73379160
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379161
feature_type: variation
id: rs1309863254
seq_region_name: 17
source: dbSNP
start: 73379161
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379163
feature_type: variation
id: rs1472323166
seq_region_name: 17
source: dbSNP
start: 73379163
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379164
feature_type: variation
id: rs1186956136
seq_region_name: 17
source: dbSNP
start: 73379164
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379167
feature_type: variation
id: rs751442576
seq_region_name: 17
source: dbSNP
start: 73379167
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379183
feature_type: variation
id: rs374754543
seq_region_name: 17
source: dbSNP
start: 73379183
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379192
feature_type: variation
id: rs1351025401
seq_region_name: 17
source: dbSNP
start: 73379192
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379193
feature_type: variation
id: rs2062809328
seq_region_name: 17
source: dbSNP
start: 73379193
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379194
feature_type: variation
id: rs1299752276
seq_region_name: 17
source: dbSNP
start: 73379194
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379197
feature_type: variation
id: rs2062809382
seq_region_name: 17
source: dbSNP
start: 73379197
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379198
feature_type: variation
id: rs754946969
seq_region_name: 17
source: dbSNP
start: 73379198
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379201
feature_type: variation
id: rs1429424023
seq_region_name: 17
source: dbSNP
start: 73379201
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379205
feature_type: variation
id: rs767623981
seq_region_name: 17
source: dbSNP
start: 73379205
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379207
feature_type: variation
id: rs1339240625
seq_region_name: 17
source: dbSNP
start: 73379207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379210
feature_type: variation
id: rs2145466309
seq_region_name: 17
source: dbSNP
start: 73379210
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379213
feature_type: variation
id: rs546934610
seq_region_name: 17
source: dbSNP
start: 73379213
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379214
feature_type: variation
id: rs568407397
seq_region_name: 17
source: dbSNP
start: 73379214
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379215
feature_type: variation
id: rs866493128
seq_region_name: 17
source: dbSNP
start: 73379215
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379217
feature_type: variation
id: rs866806553
seq_region_name: 17
source: dbSNP
start: 73379217
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379219
feature_type: variation
id: rs1599501569
seq_region_name: 17
source: dbSNP
start: 73379219
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379222
feature_type: variation
id: rs1289830769
seq_region_name: 17
source: dbSNP
start: 73379222
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379226
feature_type: variation
id: rs868590072
seq_region_name: 17
source: dbSNP
start: 73379226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379229
feature_type: variation
id: rs1364266001
seq_region_name: 17
source: dbSNP
start: 73379229
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379233
feature_type: variation
id: rs1471064479
seq_region_name: 17
source: dbSNP
start: 73379233
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73379234
feature_type: variation
id: rs778945510
seq_region_name: 17
source: dbSNP
start: 73379234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379236
feature_type: variation
id: rs1181903789
seq_region_name: 17
source: dbSNP
start: 73379236
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379238
feature_type: variation
id: rs2062809834
seq_region_name: 17
source: dbSNP
start: 73379238
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379239
feature_type: variation
id: rs1277590017
seq_region_name: 17
source: dbSNP
start: 73379239
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379244
feature_type: variation
id: rs1429189879
seq_region_name: 17
source: dbSNP
start: 73379244
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379246
feature_type: variation
id: rs1324343462
seq_region_name: 17
source: dbSNP
start: 73379246
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379247
feature_type: variation
id: rs1225469834
seq_region_name: 17
source: dbSNP
start: 73379247
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379248
feature_type: variation
id: rs2062809991
seq_region_name: 17
source: dbSNP
start: 73379248
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73379249
feature_type: variation
id: rs139388742
seq_region_name: 17
source: dbSNP
start: 73379249
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379250
feature_type: variation
id: rs758724270
seq_region_name: 17
source: dbSNP
start: 73379250
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379251
feature_type: variation
id: rs1216172745
seq_region_name: 17
source: dbSNP
start: 73379251
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379254
feature_type: variation
id: rs780372738
seq_region_name: 17
source: dbSNP
start: 73379254
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379255
feature_type: variation
id: rs150065416
seq_region_name: 17
source: dbSNP
start: 73379255
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379257
feature_type: variation
id: rs371224876
seq_region_name: 17
source: dbSNP
start: 73379257
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379258
feature_type: variation
id: rs1429617079
seq_region_name: 17
source: dbSNP
start: 73379258
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379259
feature_type: variation
id: rs1008198239
seq_region_name: 17
source: dbSNP
start: 73379259
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379261
feature_type: variation
id: rs1481114812
seq_region_name: 17
source: dbSNP
start: 73379261
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379262
feature_type: variation
id: rs1173721542
seq_region_name: 17
source: dbSNP
start: 73379262
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379263
feature_type: variation
id: rs781724733
seq_region_name: 17
source: dbSNP
start: 73379263
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379264
feature_type: variation
id: rs769364453
seq_region_name: 17
source: dbSNP
start: 73379264
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379268
feature_type: variation
id: rs772697329
seq_region_name: 17
source: dbSNP
start: 73379268
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379269
feature_type: variation
id: rs762632405
seq_region_name: 17
source: dbSNP
start: 73379269
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379270
feature_type: variation
id: rs770759494
seq_region_name: 17
source: dbSNP
start: 73379270
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379274
feature_type: variation
id: rs774277102
seq_region_name: 17
source: dbSNP
start: 73379274
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379275
feature_type: variation
id: rs1346458883
seq_region_name: 17
source: dbSNP
start: 73379275
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379278
feature_type: variation
id: rs1406827877
seq_region_name: 17
source: dbSNP
start: 73379278
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379279
feature_type: variation
id: rs2062810564
seq_region_name: 17
source: dbSNP
start: 73379279
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379284
feature_type: variation
id: rs1308914651
seq_region_name: 17
source: dbSNP
start: 73379284
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379285
feature_type: variation
id: rs1281473801
seq_region_name: 17
source: dbSNP
start: 73379285
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379286
feature_type: variation
id: rs557224263
seq_region_name: 17
source: dbSNP
start: 73379286
strand: 1
-
alleles:
- G
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73379286
feature_type: variation
id: rs1394164306
seq_region_name: 17
source: dbSNP
start: 73379286
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379287
feature_type: variation
id: rs1378409068
seq_region_name: 17
source: dbSNP
start: 73379287
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73379291
feature_type: variation
id: rs575492454
seq_region_name: 17
source: dbSNP
start: 73379291
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73379294
feature_type: variation
id: rs997630449
seq_region_name: 17
source: dbSNP
start: 73379294
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73379298
feature_type: variation
id: rs2062810760
seq_region_name: 17
source: dbSNP
start: 73379298
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379301
feature_type: variation
id: rs759474742
seq_region_name: 17
source: dbSNP
start: 73379301
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379302
feature_type: variation
id: rs973512506
seq_region_name: 17
source: dbSNP
start: 73379302
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379305
feature_type: variation
id: rs916258984
seq_region_name: 17
source: dbSNP
start: 73379305
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379306
feature_type: variation
id: rs1454709464
seq_region_name: 17
source: dbSNP
start: 73379306
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379308
feature_type: variation
id: rs1314887721
seq_region_name: 17
source: dbSNP
start: 73379308
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379310
feature_type: variation
id: rs1599501713
seq_region_name: 17
source: dbSNP
start: 73379310
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379317
feature_type: variation
id: rs767499195
seq_region_name: 17
source: dbSNP
start: 73379317
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379322
feature_type: variation
id: rs2062810946
seq_region_name: 17
source: dbSNP
start: 73379322
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379323
feature_type: variation
id: rs752694148
seq_region_name: 17
source: dbSNP
start: 73379323
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379324
feature_type: variation
id: rs886818509
seq_region_name: 17
source: dbSNP
start: 73379324
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379325
feature_type: variation
id: rs190277130
seq_region_name: 17
source: dbSNP
start: 73379325
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379326
feature_type: variation
id: rs750510486
seq_region_name: 17
source: dbSNP
start: 73379326
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379327
feature_type: variation
id: rs1885600112
seq_region_name: 17
source: dbSNP
start: 73379327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379333
feature_type: variation
id: rs1477960079
seq_region_name: 17
source: dbSNP
start: 73379333
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379334
feature_type: variation
id: rs938880078
seq_region_name: 17
source: dbSNP
start: 73379334
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379336
feature_type: variation
id: rs2062811104
seq_region_name: 17
source: dbSNP
start: 73379336
strand: 1
-
alleles:
- "-"
- GTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379338
feature_type: variation
id: rs2062811127
seq_region_name: 17
source: dbSNP
start: 73379339
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379339
feature_type: variation
id: rs2062811157
seq_region_name: 17
source: dbSNP
start: 73379339
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379340
feature_type: variation
id: rs2062811179
seq_region_name: 17
source: dbSNP
start: 73379340
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379343
feature_type: variation
id: rs2062811204
seq_region_name: 17
source: dbSNP
start: 73379343
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379344
feature_type: variation
id: rs2062811227
seq_region_name: 17
source: dbSNP
start: 73379344
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379346
feature_type: variation
id: rs1016982277
seq_region_name: 17
source: dbSNP
start: 73379346
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379348
feature_type: variation
id: rs2062811278
seq_region_name: 17
source: dbSNP
start: 73379348
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379351
feature_type: variation
id: rs962391868
seq_region_name: 17
source: dbSNP
start: 73379351
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379352
feature_type: variation
id: rs2062811311
seq_region_name: 17
source: dbSNP
start: 73379352
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379356
feature_type: variation
id: rs991586717
seq_region_name: 17
source: dbSNP
start: 73379356
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379357
feature_type: variation
id: rs1022879289
seq_region_name: 17
source: dbSNP
start: 73379357
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379362
feature_type: variation
id: rs2062811369
seq_region_name: 17
source: dbSNP
start: 73379362
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379365
feature_type: variation
id: rs1349518369
seq_region_name: 17
source: dbSNP
start: 73379362
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379364
feature_type: variation
id: rs2062811414
seq_region_name: 17
source: dbSNP
start: 73379364
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379368
feature_type: variation
id: rs753306719
seq_region_name: 17
source: dbSNP
start: 73379368
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379375
feature_type: variation
id: rs1207672274
seq_region_name: 17
source: dbSNP
start: 73379375
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379377
feature_type: variation
id: rs761254009
seq_region_name: 17
source: dbSNP
start: 73379377
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379378
feature_type: variation
id: rs557586511
seq_region_name: 17
source: dbSNP
start: 73379378
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379379
feature_type: variation
id: rs1568373057
seq_region_name: 17
source: dbSNP
start: 73379379
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379380
feature_type: variation
id: rs2145467073
seq_region_name: 17
source: dbSNP
start: 73379380
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379381
feature_type: variation
id: rs2062811555
seq_region_name: 17
source: dbSNP
start: 73379381
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379386
feature_type: variation
id: rs2062811575
seq_region_name: 17
source: dbSNP
start: 73379386
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379389
feature_type: variation
id: rs2145467101
seq_region_name: 17
source: dbSNP
start: 73379389
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379397
feature_type: variation
id: rs751268980
seq_region_name: 17
source: dbSNP
start: 73379397
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379398
feature_type: variation
id: rs2062811632
seq_region_name: 17
source: dbSNP
start: 73379398
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379400
feature_type: variation
id: rs924444286
seq_region_name: 17
source: dbSNP
start: 73379400
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379401
feature_type: variation
id: rs1321046119
seq_region_name: 17
source: dbSNP
start: 73379401
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379406
feature_type: variation
id: rs1276280046
seq_region_name: 17
source: dbSNP
start: 73379406
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379407
feature_type: variation
id: rs934710334
seq_region_name: 17
source: dbSNP
start: 73379407
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379411
feature_type: variation
id: rs758603675
seq_region_name: 17
source: dbSNP
start: 73379411
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379413
feature_type: variation
id: rs375474489
seq_region_name: 17
source: dbSNP
start: 73379413
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379418
feature_type: variation
id: rs1158479192
seq_region_name: 17
source: dbSNP
start: 73379418
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379421
feature_type: variation
id: rs3751927
seq_region_name: 17
source: dbSNP
start: 73379421
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379422
feature_type: variation
id: rs755348728
seq_region_name: 17
source: dbSNP
start: 73379422
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379423
feature_type: variation
id: rs1321630513
seq_region_name: 17
source: dbSNP
start: 73379423
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379425
feature_type: variation
id: rs781498828
seq_region_name: 17
source: dbSNP
start: 73379425
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379426
feature_type: variation
id: rs1443091323
seq_region_name: 17
source: dbSNP
start: 73379426
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379427
feature_type: variation
id: rs748717752
seq_region_name: 17
source: dbSNP
start: 73379427
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379431
feature_type: variation
id: rs1374662352
seq_region_name: 17
source: dbSNP
start: 73379431
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379432
feature_type: variation
id: rs914673156
seq_region_name: 17
source: dbSNP
start: 73379432
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379434
feature_type: variation
id: rs200215829
seq_region_name: 17
source: dbSNP
start: 73379434
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379435
feature_type: variation
id: rs777318693
seq_region_name: 17
source: dbSNP
start: 73379435
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379436
feature_type: variation
id: rs1361100406
seq_region_name: 17
source: dbSNP
start: 73379436
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379438
feature_type: variation
id: rs555332435
seq_region_name: 17
source: dbSNP
start: 73379438
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379439
feature_type: variation
id: rs187479318
seq_region_name: 17
source: dbSNP
start: 73379439
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73379440
feature_type: variation
id: rs771924342
seq_region_name: 17
source: dbSNP
start: 73379440
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73379442
feature_type: variation
id: rs775253223
seq_region_name: 17
source: dbSNP
start: 73379442
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73379445
feature_type: variation
id: rs1165942350
seq_region_name: 17
source: dbSNP
start: 73379445
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73379446
feature_type: variation
id: rs1599501883
seq_region_name: 17
source: dbSNP
start: 73379446
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379451
feature_type: variation
id: rs954608639
seq_region_name: 17
source: dbSNP
start: 73379451
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379452
feature_type: variation
id: rs983729353
seq_region_name: 17
source: dbSNP
start: 73379452
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379455
feature_type: variation
id: rs2062812257
seq_region_name: 17
source: dbSNP
start: 73379455
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379457
feature_type: variation
id: rs1178338204
seq_region_name: 17
source: dbSNP
start: 73379457
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379460
feature_type: variation
id: rs772124255
seq_region_name: 17
source: dbSNP
start: 73379460
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379466
feature_type: variation
id: rs750511145
seq_region_name: 17
source: dbSNP
start: 73379466
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379473
feature_type: variation
id: rs144878236
seq_region_name: 17
source: dbSNP
start: 73379473
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379474
feature_type: variation
id: rs141987716
seq_region_name: 17
source: dbSNP
start: 73379474
strand: 1
-
alleles:
- GGGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73379479
feature_type: variation
id: rs772983269
seq_region_name: 17
source: dbSNP
start: 73379474
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379475
feature_type: variation
id: rs2062812513
seq_region_name: 17
source: dbSNP
start: 73379475
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379477
feature_type: variation
id: rs1568373144
seq_region_name: 17
source: dbSNP
start: 73379477
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379479
feature_type: variation
id: rs145852009
seq_region_name: 17
source: dbSNP
start: 73379479
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379482
feature_type: variation
id: rs531033081
seq_region_name: 17
source: dbSNP
start: 73379482
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379485
feature_type: variation
id: rs2145467519
seq_region_name: 17
source: dbSNP
start: 73379485
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379486
feature_type: variation
id: rs2145467529
seq_region_name: 17
source: dbSNP
start: 73379486
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379488
feature_type: variation
id: rs1006829466
seq_region_name: 17
source: dbSNP
start: 73379488
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379489
feature_type: variation
id: rs753049657
seq_region_name: 17
source: dbSNP
start: 73379489
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379494
feature_type: variation
id: rs756633261
seq_region_name: 17
source: dbSNP
start: 73379494
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379495
feature_type: variation
id: rs898279246
seq_region_name: 17
source: dbSNP
start: 73379495
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379497
feature_type: variation
id: rs778213729
seq_region_name: 17
source: dbSNP
start: 73379497
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379500
feature_type: variation
id: rs981762475
seq_region_name: 17
source: dbSNP
start: 73379500
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379502
feature_type: variation
id: rs748744042
seq_region_name: 17
source: dbSNP
start: 73379502
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73379503
feature_type: variation
id: rs78145056
seq_region_name: 17
source: dbSNP
start: 73379503
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379507
feature_type: variation
id: rs2062812950
seq_region_name: 17
source: dbSNP
start: 73379507
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379508
feature_type: variation
id: rs2062812976
seq_region_name: 17
source: dbSNP
start: 73379508
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379511
feature_type: variation
id: rs778660343
seq_region_name: 17
source: dbSNP
start: 73379511
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379512
feature_type: variation
id: rs368455179
seq_region_name: 17
source: dbSNP
start: 73379512
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379515
feature_type: variation
id: rs372190160
seq_region_name: 17
source: dbSNP
start: 73379515
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379519
feature_type: variation
id: rs775335270
seq_region_name: 17
source: dbSNP
start: 73379519
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379520
feature_type: variation
id: rs865895593
seq_region_name: 17
source: dbSNP
start: 73379520
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379522
feature_type: variation
id: rs746844523
seq_region_name: 17
source: dbSNP
start: 73379522
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379523
feature_type: variation
id: rs768571029
seq_region_name: 17
source: dbSNP
start: 73379523
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379524
feature_type: variation
id: rs776562618
seq_region_name: 17
source: dbSNP
start: 73379524
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73379526
feature_type: variation
id: rs762971606
seq_region_name: 17
source: dbSNP
start: 73379526
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: stop_gained
end: 73379527
feature_type: variation
id: rs141328074
seq_region_name: 17
source: dbSNP
start: 73379527
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73379530
feature_type: variation
id: rs2062813237
seq_region_name: 17
source: dbSNP
start: 73379530
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379531
feature_type: variation
id: rs143525062
seq_region_name: 17
source: dbSNP
start: 73379531
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379532
feature_type: variation
id: rs545793892
seq_region_name: 17
source: dbSNP
start: 73379532
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73379535
feature_type: variation
id: rs373146531
seq_region_name: 17
source: dbSNP
start: 73379535
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379537
feature_type: variation
id: rs1421601439
seq_region_name: 17
source: dbSNP
start: 73379537
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73379548
feature_type: variation
id: rs2062813394
seq_region_name: 17
source: dbSNP
start: 73379548
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73379550
feature_type: variation
id: rs1465211167
seq_region_name: 17
source: dbSNP
start: 73379550
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: splice_region_variant
end: 73379554
feature_type: variation
id: rs183962646
seq_region_name: 17
source: dbSNP
start: 73379554
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73379555
feature_type: variation
id: rs764608200
seq_region_name: 17
source: dbSNP
start: 73379555
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73379556
feature_type: variation
id: rs1482029186
seq_region_name: 17
source: dbSNP
start: 73379556
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379558
feature_type: variation
id: rs754418602
seq_region_name: 17
source: dbSNP
start: 73379558
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379559
feature_type: variation
id: rs1333278079
seq_region_name: 17
source: dbSNP
start: 73379559
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379560
feature_type: variation
id: rs1210233053
seq_region_name: 17
source: dbSNP
start: 73379560
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379562
feature_type: variation
id: rs756788098
seq_region_name: 17
source: dbSNP
start: 73379562
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379563
feature_type: variation
id: rs1326582624
seq_region_name: 17
source: dbSNP
start: 73379563
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73379564
feature_type: variation
id: rs778535816
seq_region_name: 17
source: dbSNP
start: 73379564
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379567
feature_type: variation
id: rs1275705377
seq_region_name: 17
source: dbSNP
start: 73379567
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379568
feature_type: variation
id: rs568444152
seq_region_name: 17
source: dbSNP
start: 73379568
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379570
feature_type: variation
id: rs758063765
seq_region_name: 17
source: dbSNP
start: 73379570
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379571
feature_type: variation
id: rs1196319533
seq_region_name: 17
source: dbSNP
start: 73379571
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379572
feature_type: variation
id: rs947517892
seq_region_name: 17
source: dbSNP
start: 73379572
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379575
feature_type: variation
id: rs187676654
seq_region_name: 17
source: dbSNP
start: 73379575
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379577
feature_type: variation
id: rs1484561404
seq_region_name: 17
source: dbSNP
start: 73379577
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379579
feature_type: variation
id: rs746759670
seq_region_name: 17
source: dbSNP
start: 73379579
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379582
feature_type: variation
id: rs2062813748
seq_region_name: 17
source: dbSNP
start: 73379582
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379585
feature_type: variation
id: rs1255911835
seq_region_name: 17
source: dbSNP
start: 73379585
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379586
feature_type: variation
id: rs1447746300
seq_region_name: 17
source: dbSNP
start: 73379586
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379588
feature_type: variation
id: rs374118685
seq_region_name: 17
source: dbSNP
start: 73379588
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379591
feature_type: variation
id: rs1408458505
seq_region_name: 17
source: dbSNP
start: 73379590
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379591
feature_type: variation
id: rs772810009
seq_region_name: 17
source: dbSNP
start: 73379591
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379592
feature_type: variation
id: rs769768933
seq_region_name: 17
source: dbSNP
start: 73379592
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379597
feature_type: variation
id: rs1477531908
seq_region_name: 17
source: dbSNP
start: 73379597
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379598
feature_type: variation
id: rs774398614
seq_region_name: 17
source: dbSNP
start: 73379598
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379599
feature_type: variation
id: rs759602754
seq_region_name: 17
source: dbSNP
start: 73379599
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379600
feature_type: variation
id: rs2062814017
seq_region_name: 17
source: dbSNP
start: 73379600
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379607
feature_type: variation
id: rs2062814041
seq_region_name: 17
source: dbSNP
start: 73379607
strand: 1
-
alleles:
- CCCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379614
feature_type: variation
id: rs996156386
seq_region_name: 17
source: dbSNP
start: 73379611
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379612
feature_type: variation
id: rs1468938170
seq_region_name: 17
source: dbSNP
start: 73379612
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379613
feature_type: variation
id: rs1030286588
seq_region_name: 17
source: dbSNP
start: 73379613
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379621
feature_type: variation
id: rs2062814153
seq_region_name: 17
source: dbSNP
start: 73379621
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379623
feature_type: variation
id: rs1599502195
seq_region_name: 17
source: dbSNP
start: 73379623
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379624
feature_type: variation
id: rs890405895
seq_region_name: 17
source: dbSNP
start: 73379624
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379633
feature_type: variation
id: rs927386641
seq_region_name: 17
source: dbSNP
start: 73379633
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379636
feature_type: variation
id: rs2062814217
seq_region_name: 17
source: dbSNP
start: 73379636
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379640
feature_type: variation
id: rs1004810487
seq_region_name: 17
source: dbSNP
start: 73379640
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379641
feature_type: variation
id: rs2062814259
seq_region_name: 17
source: dbSNP
start: 73379641
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379642
feature_type: variation
id: rs1174711333
seq_region_name: 17
source: dbSNP
start: 73379642
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379643
feature_type: variation
id: rs1354967108
seq_region_name: 17
source: dbSNP
start: 73379643
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379644
feature_type: variation
id: rs1439510975
seq_region_name: 17
source: dbSNP
start: 73379644
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379648
feature_type: variation
id: rs962795354
seq_region_name: 17
source: dbSNP
start: 73379648
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379649
feature_type: variation
id: rs550907104
seq_region_name: 17
source: dbSNP
start: 73379649
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379650
feature_type: variation
id: rs879017750
seq_region_name: 17
source: dbSNP
start: 73379650
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379652
feature_type: variation
id: rs2062814457
seq_region_name: 17
source: dbSNP
start: 73379652
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379654
feature_type: variation
id: rs923291886
seq_region_name: 17
source: dbSNP
start: 73379654
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379655
feature_type: variation
id: rs62072075
seq_region_name: 17
source: dbSNP
start: 73379655
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379656
feature_type: variation
id: rs1226812496
seq_region_name: 17
source: dbSNP
start: 73379656
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379659
feature_type: variation
id: rs1599502252
seq_region_name: 17
source: dbSNP
start: 73379659
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379664
feature_type: variation
id: rs1284876183
seq_region_name: 17
source: dbSNP
start: 73379664
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379665
feature_type: variation
id: rs2062814621
seq_region_name: 17
source: dbSNP
start: 73379665
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379667
feature_type: variation
id: rs1280537733
seq_region_name: 17
source: dbSNP
start: 73379667
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73379775
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73379778
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73379779
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379794
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379796
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379799
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379803
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73379805
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73379805
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379807
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379810
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73379812
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379816
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379816
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379819
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379819
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379820
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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end: 73379820
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379820
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379821
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1005269823
seq_region_name: 17
source: dbSNP
start: 73379822
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1673718233
seq_region_name: 17
source: dbSNP
start: 73379823
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379825
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379830
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379838
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73379838
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379839
feature_type: variation
id: rs578170363
seq_region_name: 17
source: dbSNP
start: 73379839
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73379841
feature_type: variation
id: rs765469076
seq_region_name: 17
source: dbSNP
start: 73379841
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380071
strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- CCTTCCCC
- CCTTCCCCCTTCCCC
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73380187
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73380190
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380206
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380214
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380215
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380219
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380227
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380228
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs953561741
seq_region_name: 17
source: dbSNP
start: 73380233
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs575897434
seq_region_name: 17
source: dbSNP
start: 73380241
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380242
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062819480
seq_region_name: 17
source: dbSNP
start: 73380243
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380248
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380249
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs749181057
seq_region_name: 17
source: dbSNP
start: 73380250
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062819574
seq_region_name: 17
source: dbSNP
start: 73380256
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380258
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs938411853
seq_region_name: 17
source: dbSNP
start: 73380259
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380264
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062819637
seq_region_name: 17
source: dbSNP
start: 73380265
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs542916443
seq_region_name: 17
source: dbSNP
start: 73380269
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs145957434
seq_region_name: 17
source: dbSNP
start: 73380277
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1444584525
seq_region_name: 17
source: dbSNP
start: 73380278
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062819744
seq_region_name: 17
source: dbSNP
start: 73380282
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380283
feature_type: variation
id: rs2062819767
seq_region_name: 17
source: dbSNP
start: 73380283
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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end: 73380287
feature_type: variation
id: rs2062819789
seq_region_name: 17
source: dbSNP
start: 73380287
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380289
feature_type: variation
id: rs573401964
seq_region_name: 17
source: dbSNP
start: 73380289
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380294
feature_type: variation
id: rs768562432
seq_region_name: 17
source: dbSNP
start: 73380294
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380297
feature_type: variation
id: rs73345937
seq_region_name: 17
source: dbSNP
start: 73380297
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062819911
seq_region_name: 17
source: dbSNP
start: 73380300
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380301
feature_type: variation
id: rs1599502879
seq_region_name: 17
source: dbSNP
start: 73380301
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380303
feature_type: variation
id: rs1259299272
seq_region_name: 17
source: dbSNP
start: 73380303
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380308
feature_type: variation
id: rs147835653
seq_region_name: 17
source: dbSNP
start: 73380308
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380309
feature_type: variation
id: rs1204202478
seq_region_name: 17
source: dbSNP
start: 73380309
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380315
feature_type: variation
id: rs2062820035
seq_region_name: 17
source: dbSNP
start: 73380315
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380319
feature_type: variation
id: rs1486035318
seq_region_name: 17
source: dbSNP
start: 73380319
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380325
feature_type: variation
id: rs939189309
seq_region_name: 17
source: dbSNP
start: 73380325
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380332
feature_type: variation
id: rs187142363
seq_region_name: 17
source: dbSNP
start: 73380332
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380333
feature_type: variation
id: rs1182714118
seq_region_name: 17
source: dbSNP
start: 73380333
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380335
feature_type: variation
id: rs995958092
seq_region_name: 17
source: dbSNP
start: 73380335
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380337
feature_type: variation
id: rs1292553397
seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380525
strand: 1
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alleles:
- CCTTCGATGGGACTAGATGGGGCAGCAACCAC
- C
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380534
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73380535
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73380542
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380548
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380561
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380562
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380569
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380575
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380576
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380577
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs796812577
seq_region_name: 17
source: dbSNP
start: 73380580
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380581
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380581
strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73380717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73380728
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73380729
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73380730
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73380731
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73380758
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73380760
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380770
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73380780
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380787
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380788
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73380795
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380796
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380797
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380797
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380800
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380801
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380801
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380803
feature_type: variation
id: rs947164760
seq_region_name: 17
source: dbSNP
start: 73380803
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380805
feature_type: variation
id: rs2145471354
seq_region_name: 17
source: dbSNP
start: 73380805
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380810
feature_type: variation
id: rs2062823681
seq_region_name: 17
source: dbSNP
start: 73380810
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380815
feature_type: variation
id: rs2062823695
seq_region_name: 17
source: dbSNP
start: 73380815
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380816
feature_type: variation
id: rs111890201
seq_region_name: 17
source: dbSNP
start: 73380816
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380817
feature_type: variation
id: rs1382899168
seq_region_name: 17
source: dbSNP
start: 73380817
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380819
feature_type: variation
id: rs1285519838
seq_region_name: 17
source: dbSNP
start: 73380819
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380824
feature_type: variation
id: rs2145471396
seq_region_name: 17
source: dbSNP
start: 73380824
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380831
feature_type: variation
id: rs184468826
seq_region_name: 17
source: dbSNP
start: 73380831
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380834
feature_type: variation
id: rs2062823876
seq_region_name: 17
source: dbSNP
start: 73380831
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380832
feature_type: variation
id: rs2062823913
seq_region_name: 17
source: dbSNP
start: 73380832
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380833
feature_type: variation
id: rs573408612
seq_region_name: 17
source: dbSNP
start: 73380833
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380835
feature_type: variation
id: rs1599503341
seq_region_name: 17
source: dbSNP
start: 73380835
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380838
feature_type: variation
id: rs1318784445
seq_region_name: 17
source: dbSNP
start: 73380838
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380840
feature_type: variation
id: rs534400568
seq_region_name: 17
source: dbSNP
start: 73380840
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380842
feature_type: variation
id: rs2145471467
seq_region_name: 17
source: dbSNP
start: 73380842
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380845
feature_type: variation
id: rs201490153
seq_region_name: 17
source: dbSNP
start: 73380845
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380847
feature_type: variation
id: rs1171738892
seq_region_name: 17
source: dbSNP
start: 73380847
strand: 1
-
alleles:
- CT
- CTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380848
feature_type: variation
id: rs2062824154
seq_region_name: 17
source: dbSNP
start: 73380847
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380848
feature_type: variation
id: rs775589284
seq_region_name: 17
source: dbSNP
start: 73380848
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380849
feature_type: variation
id: rs1383757730
seq_region_name: 17
source: dbSNP
start: 73380849
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380850
feature_type: variation
id: rs370093905
seq_region_name: 17
source: dbSNP
start: 73380850
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380851
feature_type: variation
id: rs574231940
seq_region_name: 17
source: dbSNP
start: 73380851
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380859
feature_type: variation
id: rs1405020392
seq_region_name: 17
source: dbSNP
start: 73380859
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380861
feature_type: variation
id: rs754297993
seq_region_name: 17
source: dbSNP
start: 73380861
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380863
feature_type: variation
id: rs544693975
seq_region_name: 17
source: dbSNP
start: 73380863
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380864
feature_type: variation
id: rs373540764
seq_region_name: 17
source: dbSNP
start: 73380864
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380865
feature_type: variation
id: rs73999012
seq_region_name: 17
source: dbSNP
start: 73380865
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380866
feature_type: variation
id: rs890797483
seq_region_name: 17
source: dbSNP
start: 73380866
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380868
feature_type: variation
id: rs940527866
seq_region_name: 17
source: dbSNP
start: 73380868
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380869
feature_type: variation
id: rs757856941
seq_region_name: 17
source: dbSNP
start: 73380869
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380875
feature_type: variation
id: rs1036235078
seq_region_name: 17
source: dbSNP
start: 73380875
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380876
feature_type: variation
id: rs1284126231
seq_region_name: 17
source: dbSNP
start: 73380876
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380877
feature_type: variation
id: rs2062824530
seq_region_name: 17
source: dbSNP
start: 73380877
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380880
feature_type: variation
id: rs2062824560
seq_region_name: 17
source: dbSNP
start: 73380880
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380882
feature_type: variation
id: rs2062824590
seq_region_name: 17
source: dbSNP
start: 73380882
strand: 1
-
alleles:
- AGGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380887
feature_type: variation
id: rs1488093612
seq_region_name: 17
source: dbSNP
start: 73380883
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380885
feature_type: variation
id: rs779704701
seq_region_name: 17
source: dbSNP
start: 73380885
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73380889
feature_type: variation
id: rs545027699
seq_region_name: 17
source: dbSNP
start: 73380889
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73380893
feature_type: variation
id: rs751198523
seq_region_name: 17
source: dbSNP
start: 73380893
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380897
feature_type: variation
id: rs1212419234
seq_region_name: 17
source: dbSNP
start: 73380897
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380901
feature_type: variation
id: rs560405975
seq_region_name: 17
source: dbSNP
start: 73380901
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380903
feature_type: variation
id: rs80234264
seq_region_name: 17
source: dbSNP
start: 73380903
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380904
feature_type: variation
id: rs994948082
seq_region_name: 17
source: dbSNP
start: 73380904
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380905
feature_type: variation
id: rs2062824842
seq_region_name: 17
source: dbSNP
start: 73380905
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380910
feature_type: variation
id: rs141769892
seq_region_name: 17
source: dbSNP
start: 73380910
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380911
feature_type: variation
id: rs769720071
seq_region_name: 17
source: dbSNP
start: 73380911
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380912
feature_type: variation
id: rs1302399371
seq_region_name: 17
source: dbSNP
start: 73380912
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380913
feature_type: variation
id: rs1359439966
seq_region_name: 17
source: dbSNP
start: 73380913
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380916
feature_type: variation
id: rs1424910873
seq_region_name: 17
source: dbSNP
start: 73380916
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380919
feature_type: variation
id: rs2062825001
seq_region_name: 17
source: dbSNP
start: 73380919
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380920
feature_type: variation
id: rs1304392507
seq_region_name: 17
source: dbSNP
start: 73380920
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380922
feature_type: variation
id: rs1405519413
seq_region_name: 17
source: dbSNP
start: 73380922
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73380923
feature_type: variation
id: rs777693190
seq_region_name: 17
source: dbSNP
start: 73380923
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380924
feature_type: variation
id: rs1351663972
seq_region_name: 17
source: dbSNP
start: 73380924
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380927
feature_type: variation
id: rs1385769546
seq_region_name: 17
source: dbSNP
start: 73380927
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380928
feature_type: variation
id: rs745903296
seq_region_name: 17
source: dbSNP
start: 73380928
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380929
feature_type: variation
id: rs1336927066
seq_region_name: 17
source: dbSNP
start: 73380929
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380930
feature_type: variation
id: rs1242694814
seq_region_name: 17
source: dbSNP
start: 73380930
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380931
feature_type: variation
id: rs1307537837
seq_region_name: 17
source: dbSNP
start: 73380931
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380933
feature_type: variation
id: rs2145471845
seq_region_name: 17
source: dbSNP
start: 73380933
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73380935
feature_type: variation
id: rs764376018
seq_region_name: 17
source: dbSNP
start: 73380935
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73380936
feature_type: variation
id: rs370912779
seq_region_name: 17
source: dbSNP
start: 73380936
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380938
feature_type: variation
id: rs2062825362
seq_region_name: 17
source: dbSNP
start: 73380938
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73380940
feature_type: variation
id: rs1267509990
seq_region_name: 17
source: dbSNP
start: 73380940
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380941
feature_type: variation
id: rs2145471876
seq_region_name: 17
source: dbSNP
start: 73380941
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380942
feature_type: variation
id: rs2062825403
seq_region_name: 17
source: dbSNP
start: 73380942
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73380942
feature_type: variation
id: rs2062825427
seq_region_name: 17
source: dbSNP
start: 73380942
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380946
feature_type: variation
id: rs2062825450
seq_region_name: 17
source: dbSNP
start: 73380946
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380947
feature_type: variation
id: rs1420564369
seq_region_name: 17
source: dbSNP
start: 73380947
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380948
feature_type: variation
id: rs1487529701
seq_region_name: 17
source: dbSNP
start: 73380948
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380949
feature_type: variation
id: rs2062825510
seq_region_name: 17
source: dbSNP
start: 73380949
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73380950
feature_type: variation
id: rs1209386474
seq_region_name: 17
source: dbSNP
start: 73380950
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73380951
feature_type: variation
id: rs2062825557
seq_region_name: 17
source: dbSNP
start: 73380951
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: splice_region_variant
end: 73380953
feature_type: variation
id: rs2062825575
seq_region_name: 17
source: dbSNP
start: 73380953
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380954
feature_type: variation
id: rs1233654835
seq_region_name: 17
source: dbSNP
start: 73380954
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380955
feature_type: variation
id: rs777126059
seq_region_name: 17
source: dbSNP
start: 73380955
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380958
feature_type: variation
id: rs1555755560
seq_region_name: 17
source: dbSNP
start: 73380955
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380956
feature_type: variation
id: rs762270223
seq_region_name: 17
source: dbSNP
start: 73380956
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380957
feature_type: variation
id: rs374092221
seq_region_name: 17
source: dbSNP
start: 73380957
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73380958
feature_type: variation
id: rs1267334539
seq_region_name: 17
source: dbSNP
start: 73380958
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73380959
feature_type: variation
id: rs1379493754
seq_region_name: 17
source: dbSNP
start: 73380959
strand: 1
-
alleles:
- GGGGG
- GGGGGG
- GGGGGGG
- GGGGGGGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73380964
feature_type: variation
id: rs1489784214
seq_region_name: 17
source: dbSNP
start: 73380960
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73380962
feature_type: variation
id: rs1247918933
seq_region_name: 17
source: dbSNP
start: 73380962
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs762481061
seq_region_name: 17
source: dbSNP
start: 73380964
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380965
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145472068
seq_region_name: 17
source: dbSNP
start: 73380965
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1165050325
seq_region_name: 17
source: dbSNP
start: 73380966
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs2062825897
seq_region_name: 17
source: dbSNP
start: 73380966
strand: 1
-
alleles:
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- GCCGGGGCGGGGGCGCCGGGGCGGGGGCGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568373880
seq_region_name: 17
source: dbSNP
start: 73380966
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs765775408
seq_region_name: 17
source: dbSNP
start: 73380967
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062825969
seq_region_name: 17
source: dbSNP
start: 73380967
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs751128775
seq_region_name: 17
source: dbSNP
start: 73380968
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs754611415
seq_region_name: 17
source: dbSNP
start: 73380969
strand: 1
-
alleles:
- GG
- GGCTGGTTTACCTGGGTTTGGGGGGGGGGGGGGGGG
- GGTTTGTTTAACTGGGTTTGGGGGGGGGGGGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380970
feature_type: variation
id: rs2145472140
seq_region_name: 17
source: dbSNP
start: 73380969
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1298260465
seq_region_name: 17
source: dbSNP
start: 73380970
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73380971
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs780887767
seq_region_name: 17
source: dbSNP
start: 73380972
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145472177
seq_region_name: 17
source: dbSNP
start: 73380972
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1449690412
seq_region_name: 17
source: dbSNP
start: 73380973
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1307464628
seq_region_name: 17
source: dbSNP
start: 73380974
strand: 1
-
alleles:
- GGGGG
- GGGGGGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062826187
seq_region_name: 17
source: dbSNP
start: 73380974
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs994107987
seq_region_name: 17
source: dbSNP
start: 73380976
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs752424909
seq_region_name: 17
source: dbSNP
start: 73380979
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1247226823
seq_region_name: 17
source: dbSNP
start: 73380980
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062826280
seq_region_name: 17
source: dbSNP
start: 73380982
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062826320
seq_region_name: 17
source: dbSNP
start: 73380983
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs755918552
seq_region_name: 17
source: dbSNP
start: 73380986
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1320205154
seq_region_name: 17
source: dbSNP
start: 73380987
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380991
feature_type: variation
id: rs1244087407
seq_region_name: 17
source: dbSNP
start: 73380991
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73380994
feature_type: variation
id: rs1251974304
seq_region_name: 17
source: dbSNP
start: 73380994
strand: 1
-
alleles:
- GAGGAGG
- GAGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381006
feature_type: variation
id: rs1568373922
seq_region_name: 17
source: dbSNP
start: 73381000
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062826461
seq_region_name: 17
source: dbSNP
start: 73381003
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381005
feature_type: variation
id: rs956975957
seq_region_name: 17
source: dbSNP
start: 73381005
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs952152496
seq_region_name: 17
source: dbSNP
start: 73381007
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062826535
seq_region_name: 17
source: dbSNP
start: 73381011
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062826562
seq_region_name: 17
source: dbSNP
start: 73381012
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381015
feature_type: variation
id: rs1010114790
seq_region_name: 17
source: dbSNP
start: 73381015
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381017
feature_type: variation
id: rs2062826603
seq_region_name: 17
source: dbSNP
start: 73381017
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381018
feature_type: variation
id: rs1177656740
seq_region_name: 17
source: dbSNP
start: 73381018
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381019
feature_type: variation
id: rs2062826641
seq_region_name: 17
source: dbSNP
start: 73381019
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381023
feature_type: variation
id: rs2062826669
seq_region_name: 17
source: dbSNP
start: 73381023
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381025
feature_type: variation
id: rs1435425630
seq_region_name: 17
source: dbSNP
start: 73381025
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381027
feature_type: variation
id: rs1406505359
seq_region_name: 17
source: dbSNP
start: 73381027
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381028
feature_type: variation
id: rs189138070
seq_region_name: 17
source: dbSNP
start: 73381028
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381029
feature_type: variation
id: rs1177148640
seq_region_name: 17
source: dbSNP
start: 73381029
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381030
feature_type: variation
id: rs1568373938
seq_region_name: 17
source: dbSNP
start: 73381030
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381032
feature_type: variation
id: rs2145472419
seq_region_name: 17
source: dbSNP
start: 73381032
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381043
feature_type: variation
id: rs892173307
seq_region_name: 17
source: dbSNP
start: 73381043
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381044
feature_type: variation
id: rs182278527
seq_region_name: 17
source: dbSNP
start: 73381044
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381050
feature_type: variation
id: rs2062826825
seq_region_name: 17
source: dbSNP
start: 73381050
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381051
feature_type: variation
id: rs1194367159
seq_region_name: 17
source: dbSNP
start: 73381051
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381052
feature_type: variation
id: rs1459732111
seq_region_name: 17
source: dbSNP
start: 73381052
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381054
feature_type: variation
id: rs1568373956
seq_region_name: 17
source: dbSNP
start: 73381054
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381056
feature_type: variation
id: rs1262272239
seq_region_name: 17
source: dbSNP
start: 73381056
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381060
feature_type: variation
id: rs185568229
seq_region_name: 17
source: dbSNP
start: 73381060
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381061
feature_type: variation
id: rs921715485
seq_region_name: 17
source: dbSNP
start: 73381061
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381063
feature_type: variation
id: rs953032007
seq_region_name: 17
source: dbSNP
start: 73381063
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381064
feature_type: variation
id: rs549483445
seq_region_name: 17
source: dbSNP
start: 73381064
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381069
feature_type: variation
id: rs571229007
seq_region_name: 17
source: dbSNP
start: 73381069
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381070
feature_type: variation
id: rs2145472508
seq_region_name: 17
source: dbSNP
start: 73381070
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381073
feature_type: variation
id: rs979272068
seq_region_name: 17
source: dbSNP
start: 73381073
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381078
feature_type: variation
id: rs1599503710
seq_region_name: 17
source: dbSNP
start: 73381078
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381082
feature_type: variation
id: rs1599503715
seq_region_name: 17
source: dbSNP
start: 73381082
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381087
feature_type: variation
id: rs925118384
seq_region_name: 17
source: dbSNP
start: 73381087
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381091
feature_type: variation
id: rs2145472551
seq_region_name: 17
source: dbSNP
start: 73381091
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381093
feature_type: variation
id: rs2062827150
seq_region_name: 17
source: dbSNP
start: 73381093
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381094
feature_type: variation
id: rs2062827165
seq_region_name: 17
source: dbSNP
start: 73381094
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381095
feature_type: variation
id: rs1405718063
seq_region_name: 17
source: dbSNP
start: 73381095
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381096
feature_type: variation
id: rs2062827203
seq_region_name: 17
source: dbSNP
start: 73381096
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381098
feature_type: variation
id: rs1337791107
seq_region_name: 17
source: dbSNP
start: 73381098
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381100
feature_type: variation
id: rs940628197
seq_region_name: 17
source: dbSNP
start: 73381100
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381101
feature_type: variation
id: rs2062827271
seq_region_name: 17
source: dbSNP
start: 73381101
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381105
feature_type: variation
id: rs2062827293
seq_region_name: 17
source: dbSNP
start: 73381105
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381109
feature_type: variation
id: rs538629169
seq_region_name: 17
source: dbSNP
start: 73381109
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381110
feature_type: variation
id: rs1161970714
seq_region_name: 17
source: dbSNP
start: 73381110
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381112
feature_type: variation
id: rs2062827382
seq_region_name: 17
source: dbSNP
start: 73381110
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381111
feature_type: variation
id: rs1599503740
seq_region_name: 17
source: dbSNP
start: 73381111
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381114
feature_type: variation
id: rs1389731865
seq_region_name: 17
source: dbSNP
start: 73381114
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381116
feature_type: variation
id: rs920460013
seq_region_name: 17
source: dbSNP
start: 73381116
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381118
feature_type: variation
id: rs1401015585
seq_region_name: 17
source: dbSNP
start: 73381118
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381119
feature_type: variation
id: rs2062827474
seq_region_name: 17
source: dbSNP
start: 73381119
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381122
feature_type: variation
id: rs1442378669
seq_region_name: 17
source: dbSNP
start: 73381122
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381123
feature_type: variation
id: rs1242080658
seq_region_name: 17
source: dbSNP
start: 73381123
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381128
feature_type: variation
id: rs2145472693
seq_region_name: 17
source: dbSNP
start: 73381128
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381129
feature_type: variation
id: rs1182087474
seq_region_name: 17
source: dbSNP
start: 73381129
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381129
feature_type: variation
id: rs1484086860
seq_region_name: 17
source: dbSNP
start: 73381129
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381131
feature_type: variation
id: rs1049489024
seq_region_name: 17
source: dbSNP
start: 73381131
strand: 1
-
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-
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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- C
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381185
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73381187
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381191
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381205
strand: 1
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alleles:
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- G
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381208
strand: 1
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alleles:
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- G
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381210
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73381216
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381225
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381230
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381233
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381239
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381242
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381243
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381244
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381245
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381247
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381248
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381250
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381254
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381255
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381257
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381257
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs547035071
seq_region_name: 17
source: dbSNP
start: 73381258
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381260
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1488569752
seq_region_name: 17
source: dbSNP
start: 73381261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381263
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381265
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73381267
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381270
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1266136571
seq_region_name: 17
source: dbSNP
start: 73381282
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062828679
seq_region_name: 17
source: dbSNP
start: 73381288
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062828704
seq_region_name: 17
source: dbSNP
start: 73381291
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381294
feature_type: variation
id: rs2062828723
seq_region_name: 17
source: dbSNP
start: 73381294
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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end: 73381298
feature_type: variation
id: rs2062828757
seq_region_name: 17
source: dbSNP
start: 73381298
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381304
feature_type: variation
id: rs1247236282
seq_region_name: 17
source: dbSNP
start: 73381304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381305
feature_type: variation
id: rs2145473281
seq_region_name: 17
source: dbSNP
start: 73381305
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381307
feature_type: variation
id: rs1286813486
seq_region_name: 17
source: dbSNP
start: 73381307
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381308
feature_type: variation
id: rs79358180
seq_region_name: 17
source: dbSNP
start: 73381308
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381309
feature_type: variation
id: rs2062828863
seq_region_name: 17
source: dbSNP
start: 73381309
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381310
feature_type: variation
id: rs1295284211
seq_region_name: 17
source: dbSNP
start: 73381310
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381313
feature_type: variation
id: rs1022862238
seq_region_name: 17
source: dbSNP
start: 73381313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381314
feature_type: variation
id: rs1342773871
seq_region_name: 17
source: dbSNP
start: 73381314
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381315
feature_type: variation
id: rs2062828955
seq_region_name: 17
source: dbSNP
start: 73381315
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381324
feature_type: variation
id: rs1014036353
seq_region_name: 17
source: dbSNP
start: 73381324
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381325
feature_type: variation
id: rs2062828999
seq_region_name: 17
source: dbSNP
start: 73381325
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381328
feature_type: variation
id: rs534490685
seq_region_name: 17
source: dbSNP
start: 73381328
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1243813901
seq_region_name: 17
source: dbSNP
start: 73381335
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381340
feature_type: variation
id: rs968224692
seq_region_name: 17
source: dbSNP
start: 73381340
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381341
feature_type: variation
id: rs2062829073
seq_region_name: 17
source: dbSNP
start: 73381341
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381347
feature_type: variation
id: rs2145473375
seq_region_name: 17
source: dbSNP
start: 73381347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381349
feature_type: variation
id: rs997451178
seq_region_name: 17
source: dbSNP
start: 73381349
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381351
feature_type: variation
id: rs35551526
seq_region_name: 17
source: dbSNP
start: 73381351
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381353
feature_type: variation
id: rs112743415
seq_region_name: 17
source: dbSNP
start: 73381353
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381355
feature_type: variation
id: rs1169325732
seq_region_name: 17
source: dbSNP
start: 73381355
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381475
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381475
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381478
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381483
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381488
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381500
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381504
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381513
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381519
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381522
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381523
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381533
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381534
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381537
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381538
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381541
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381543
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs566010630
seq_region_name: 17
source: dbSNP
start: 73381547
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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end: 73381548
feature_type: variation
id: rs1021420893
seq_region_name: 17
source: dbSNP
start: 73381548
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381555
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1379734529
seq_region_name: 17
source: dbSNP
start: 73381556
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062830434
seq_region_name: 17
source: dbSNP
start: 73381558
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381561
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381564
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381566
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062830521
seq_region_name: 17
source: dbSNP
start: 73381567
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062830539
seq_region_name: 17
source: dbSNP
start: 73381569
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381571
feature_type: variation
id: rs1568374262
seq_region_name: 17
source: dbSNP
start: 73381571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599504089
seq_region_name: 17
source: dbSNP
start: 73381576
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs748052366
seq_region_name: 17
source: dbSNP
start: 73381580
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381581
feature_type: variation
id: rs545427460
seq_region_name: 17
source: dbSNP
start: 73381581
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381582
feature_type: variation
id: rs2145473990
seq_region_name: 17
source: dbSNP
start: 73381582
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381589
feature_type: variation
id: rs2062830642
seq_region_name: 17
source: dbSNP
start: 73381589
strand: 1
-
alleles:
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- GA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381593
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381589
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1183229821
seq_region_name: 17
source: dbSNP
start: 73381596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062830745
seq_region_name: 17
source: dbSNP
start: 73381598
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062830769
seq_region_name: 17
source: dbSNP
start: 73381600
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381602
feature_type: variation
id: rs538230156
seq_region_name: 17
source: dbSNP
start: 73381602
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381603
feature_type: variation
id: rs1281197146
seq_region_name: 17
source: dbSNP
start: 73381603
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381605
feature_type: variation
id: rs1203881048
seq_region_name: 17
source: dbSNP
start: 73381605
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381606
feature_type: variation
id: rs1056450580
seq_region_name: 17
source: dbSNP
start: 73381606
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381607
feature_type: variation
id: rs1264236075
seq_region_name: 17
source: dbSNP
start: 73381607
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
-
alleles:
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- GA
assembly_name: GRCh38
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strand: 1
-
alleles:
- CACCTGAGGTCAGGAGTTCGAGACCACCTGAGGTCAGGAGTTCGAGAC
- CACCTGAGGTCAGGAGTTCGAGAC
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assembly_name: GRCh38
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alleles:
- ACCT
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73381700
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alleles:
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assembly_name: GRCh38
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start: 73381701
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381714
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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start: 73381715
strand: 1
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alleles:
- C
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381717
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381722
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381723
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381725
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381730
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381732
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73381733
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381740
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381743
strand: 1
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alleles:
- C
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assembly_name: GRCh38
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start: 73381748
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73381755
strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73381762
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73381765
strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73381770
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381772
strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381774
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs961725552
seq_region_name: 17
source: dbSNP
start: 73381777
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381778
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062832994
seq_region_name: 17
source: dbSNP
start: 73381779
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs909497475
seq_region_name: 17
source: dbSNP
start: 73381780
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1416305380
seq_region_name: 17
source: dbSNP
start: 73381781
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1166386515
seq_region_name: 17
source: dbSNP
start: 73381784
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062833070
seq_region_name: 17
source: dbSNP
start: 73381785
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145474601
seq_region_name: 17
source: dbSNP
start: 73381786
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062833112
seq_region_name: 17
source: dbSNP
start: 73381790
strand: 1
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alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73381796
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381799
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs938240074
seq_region_name: 17
source: dbSNP
start: 73381802
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381803
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381804
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062833308
seq_region_name: 17
source: dbSNP
start: 73381807
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381810
feature_type: variation
id: rs1027570612
seq_region_name: 17
source: dbSNP
start: 73381810
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381812
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381812
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381813
feature_type: variation
id: rs1244470262
seq_region_name: 17
source: dbSNP
start: 73381813
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381815
feature_type: variation
id: rs746611810
seq_region_name: 17
source: dbSNP
start: 73381815
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73381819
feature_type: variation
id: rs770686101
seq_region_name: 17
source: dbSNP
start: 73381819
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73381930
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73381934
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73381945
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73381947
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381953
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381963
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73381968
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381972
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73381975
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73381980
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73381986
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381987
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381994
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73381998
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs926947064
seq_region_name: 17
source: dbSNP
start: 73382001
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1482123668
seq_region_name: 17
source: dbSNP
start: 73382004
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382005
feature_type: variation
id: rs2062835069
seq_region_name: 17
source: dbSNP
start: 73382005
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382006
feature_type: variation
id: rs1236729152
seq_region_name: 17
source: dbSNP
start: 73382006
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382012
feature_type: variation
id: rs891278431
seq_region_name: 17
source: dbSNP
start: 73382012
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382013
feature_type: variation
id: rs373388462
seq_region_name: 17
source: dbSNP
start: 73382013
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382016
feature_type: variation
id: rs958324890
seq_region_name: 17
source: dbSNP
start: 73382016
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382019
feature_type: variation
id: rs1283955063
seq_region_name: 17
source: dbSNP
start: 73382019
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1239444116
seq_region_name: 17
source: dbSNP
start: 73382020
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382021
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id: rs1354507065
seq_region_name: 17
source: dbSNP
start: 73382021
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382023
feature_type: variation
id: rs1311686613
seq_region_name: 17
source: dbSNP
start: 73382023
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382025
feature_type: variation
id: rs1599504559
seq_region_name: 17
source: dbSNP
start: 73382025
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382027
feature_type: variation
id: rs1008381660
seq_region_name: 17
source: dbSNP
start: 73382027
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382034
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id: rs1394533808
seq_region_name: 17
source: dbSNP
start: 73382033
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382036
feature_type: variation
id: rs1378875506
seq_region_name: 17
source: dbSNP
start: 73382036
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382107
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs925287183
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1290184444
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382116
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382122
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382131
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382132
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382134
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382141
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382148
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1294144299
seq_region_name: 17
source: dbSNP
start: 73382155
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs767365640
seq_region_name: 17
source: dbSNP
start: 73382156
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1425292258
seq_region_name: 17
source: dbSNP
start: 73382160
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382171
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062836546
seq_region_name: 17
source: dbSNP
start: 73382175
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs912851295
seq_region_name: 17
source: dbSNP
start: 73382177
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1320145065
seq_region_name: 17
source: dbSNP
start: 73382178
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062836573
seq_region_name: 17
source: dbSNP
start: 73382179
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382183
feature_type: variation
id: rs138329333
seq_region_name: 17
source: dbSNP
start: 73382183
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1478130429
seq_region_name: 17
source: dbSNP
start: 73382184
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599504687
seq_region_name: 17
source: dbSNP
start: 73382195
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382198
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062836667
seq_region_name: 17
source: dbSNP
start: 73382203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062836684
seq_region_name: 17
source: dbSNP
start: 73382204
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382205
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382205
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382210
feature_type: variation
id: rs1599504697
seq_region_name: 17
source: dbSNP
start: 73382210
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382211
feature_type: variation
id: rs1016125677
seq_region_name: 17
source: dbSNP
start: 73382211
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382212
feature_type: variation
id: rs2062836750
seq_region_name: 17
source: dbSNP
start: 73382212
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382213
feature_type: variation
id: rs2062836777
seq_region_name: 17
source: dbSNP
start: 73382212
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382215
feature_type: variation
id: rs2062836799
seq_region_name: 17
source: dbSNP
start: 73382215
strand: 1
-
alleles:
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- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382217
feature_type: variation
id: rs2062836836
seq_region_name: 17
source: dbSNP
start: 73382215
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382218
feature_type: variation
id: rs753823973
seq_region_name: 17
source: dbSNP
start: 73382218
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382218
feature_type: variation
id: rs963526200
seq_region_name: 17
source: dbSNP
start: 73382218
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382219
feature_type: variation
id: rs773076847
seq_region_name: 17
source: dbSNP
start: 73382218
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382219
feature_type: variation
id: rs63085260
seq_region_name: 17
source: dbSNP
start: 73382219
strand: 1
-
alleles:
- AAAAAAAAAAAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382235
feature_type: variation
id: rs34453546
seq_region_name: 17
source: dbSNP
start: 73382219
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382220
feature_type: variation
id: rs2062837039
seq_region_name: 17
source: dbSNP
start: 73382220
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382224
feature_type: variation
id: rs2062837067
seq_region_name: 17
source: dbSNP
start: 73382224
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382225
feature_type: variation
id: rs2062837084
seq_region_name: 17
source: dbSNP
start: 73382225
strand: 1
-
alleles:
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- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382238
feature_type: variation
id: rs1299834103
seq_region_name: 17
source: dbSNP
start: 73382232
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382233
feature_type: variation
id: rs78812804
seq_region_name: 17
source: dbSNP
start: 73382233
strand: 1
-
alleles:
- AAAGAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382238
feature_type: variation
id: rs1568374536
seq_region_name: 17
source: dbSNP
start: 73382233
strand: 1
-
alleles:
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- AAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382240
feature_type: variation
id: rs2145475942
seq_region_name: 17
source: dbSNP
start: 73382234
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382235
feature_type: variation
id: rs1427659989
seq_region_name: 17
source: dbSNP
start: 73382235
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382236
feature_type: variation
id: rs974193801
seq_region_name: 17
source: dbSNP
start: 73382236
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382236
feature_type: variation
id: rs1389424199
seq_region_name: 17
source: dbSNP
start: 73382236
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382239
feature_type: variation
id: rs944208905
seq_region_name: 17
source: dbSNP
start: 73382239
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382240
feature_type: variation
id: rs2145475978
seq_region_name: 17
source: dbSNP
start: 73382240
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382243
feature_type: variation
id: rs1486794274
seq_region_name: 17
source: dbSNP
start: 73382243
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382244
feature_type: variation
id: rs1186638904
seq_region_name: 17
source: dbSNP
start: 73382244
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382245
feature_type: variation
id: rs1037609522
seq_region_name: 17
source: dbSNP
start: 73382245
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382248
feature_type: variation
id: rs1599504781
seq_region_name: 17
source: dbSNP
start: 73382248
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382254
feature_type: variation
id: rs1599504783
seq_region_name: 17
source: dbSNP
start: 73382254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062837709
seq_region_name: 17
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start: 73382309
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73382341
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73382346
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73382347
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382348
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382349
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1442642001
seq_region_name: 17
source: dbSNP
start: 73382353
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382355
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1286056785
seq_region_name: 17
source: dbSNP
start: 73382361
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062838158
seq_region_name: 17
source: dbSNP
start: 73382362
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382370
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382372
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382375
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1374274681
seq_region_name: 17
source: dbSNP
start: 73382376
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599504882
seq_region_name: 17
source: dbSNP
start: 73382377
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382379
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382380
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seq_region_name: 17
source: dbSNP
start: 73382380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382383
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382385
feature_type: variation
id: rs1465888286
seq_region_name: 17
source: dbSNP
start: 73382385
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382387
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382399
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73382401
feature_type: variation
id: rs567932285
seq_region_name: 17
source: dbSNP
start: 73382401
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382404
feature_type: variation
id: rs79125057
seq_region_name: 17
source: dbSNP
start: 73382404
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs556471743
seq_region_name: 17
source: dbSNP
start: 73382407
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382408
feature_type: variation
id: rs2062838426
seq_region_name: 17
source: dbSNP
start: 73382408
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382410
feature_type: variation
id: rs2145476487
seq_region_name: 17
source: dbSNP
start: 73382410
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382415
feature_type: variation
id: rs1599504900
seq_region_name: 17
source: dbSNP
start: 73382415
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs954039677
seq_region_name: 17
source: dbSNP
start: 73382417
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382418
feature_type: variation
id: rs571760540
seq_region_name: 17
source: dbSNP
start: 73382418
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382420
feature_type: variation
id: rs1175662511
seq_region_name: 17
source: dbSNP
start: 73382420
strand: 1
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alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382422
feature_type: variation
id: rs1206606754
seq_region_name: 17
source: dbSNP
start: 73382422
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382423
feature_type: variation
id: rs2062838636
seq_region_name: 17
source: dbSNP
start: 73382423
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382428
feature_type: variation
id: rs936813762
seq_region_name: 17
source: dbSNP
start: 73382428
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382429
feature_type: variation
id: rs2062838686
seq_region_name: 17
source: dbSNP
start: 73382429
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382432
feature_type: variation
id: rs1461739424
seq_region_name: 17
source: dbSNP
start: 73382432
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382442
feature_type: variation
id: rs2062838714
seq_region_name: 17
source: dbSNP
start: 73382442
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382448
feature_type: variation
id: rs556424612
seq_region_name: 17
source: dbSNP
start: 73382448
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382449
feature_type: variation
id: rs1053819106
seq_region_name: 17
source: dbSNP
start: 73382449
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382455
feature_type: variation
id: rs2062838770
seq_region_name: 17
source: dbSNP
start: 73382455
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382460
feature_type: variation
id: rs2062838794
seq_region_name: 17
source: dbSNP
start: 73382460
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382464
feature_type: variation
id: rs538736609
seq_region_name: 17
source: dbSNP
start: 73382464
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382465
feature_type: variation
id: rs1235297484
seq_region_name: 17
source: dbSNP
start: 73382465
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382469
feature_type: variation
id: rs912776111
seq_region_name: 17
source: dbSNP
start: 73382469
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382475
feature_type: variation
id: rs1346414188
seq_region_name: 17
source: dbSNP
start: 73382475
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382476
feature_type: variation
id: rs942746093
seq_region_name: 17
source: dbSNP
start: 73382476
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382479
feature_type: variation
id: rs1235781650
seq_region_name: 17
source: dbSNP
start: 73382479
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382480
feature_type: variation
id: rs554174284
seq_region_name: 17
source: dbSNP
start: 73382480
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382482
feature_type: variation
id: rs1568374615
seq_region_name: 17
source: dbSNP
start: 73382482
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382484
feature_type: variation
id: rs1177498066
seq_region_name: 17
source: dbSNP
start: 73382484
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382486
feature_type: variation
id: rs2145476649
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73382619
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73382634
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73382646
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382647
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382650
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382652
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382656
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382660
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73382661
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382662
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382663
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73382664
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73382666
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382668
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145477106
seq_region_name: 17
source: dbSNP
start: 73382682
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382685
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382686
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382687
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73382692
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382696
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867361894
seq_region_name: 17
source: dbSNP
start: 73382703
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382705
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382710
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382712
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382718
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382718
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73382719
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382719
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382721
feature_type: variation
id: rs1323089354
seq_region_name: 17
source: dbSNP
start: 73382721
strand: 1
-
alleles:
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- G
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382847
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73382850
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382852
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382852
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73382855
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- "-"
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382858
strand: 1
-
alleles:
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- AC
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- ACAACAACAAC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73382860
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382861
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382862
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382866
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382870
strand: 1
-
alleles:
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- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382871
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1204050232
seq_region_name: 17
source: dbSNP
start: 73382872
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382873
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73382873
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382874
feature_type: variation
id: rs2145477605
seq_region_name: 17
source: dbSNP
start: 73382874
strand: 1
-
alleles:
- ACAACA
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73382879
feature_type: variation
id: rs1438743902
seq_region_name: 17
source: dbSNP
start: 73382874
strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73383030
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73383055
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383063
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383070
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383071
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383075
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383075
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383082
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383083
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73383085
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1429157969
seq_region_name: 17
source: dbSNP
start: 73383086
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383093
strand: 1
-
alleles:
- GCCTCGGTCCACCCCGAGTCTGTGCCTCGGT
- GCCTCGGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062844730
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source: dbSNP
start: 73383101
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1263993199
seq_region_name: 17
source: dbSNP
start: 73383103
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs144850975
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599505634
seq_region_name: 17
source: dbSNP
start: 73383111
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs949891692
seq_region_name: 17
source: dbSNP
start: 73383113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1045914537
seq_region_name: 17
source: dbSNP
start: 73383115
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs563689266
seq_region_name: 17
source: dbSNP
start: 73383116
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062844911
seq_region_name: 17
source: dbSNP
start: 73383119
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062844929
seq_region_name: 17
source: dbSNP
start: 73383121
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568374919
seq_region_name: 17
source: dbSNP
start: 73383124
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1228849762
seq_region_name: 17
source: dbSNP
start: 73383128
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1307545667
seq_region_name: 17
source: dbSNP
start: 73383129
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1297175517
seq_region_name: 17
source: dbSNP
start: 73383136
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs571734487
seq_region_name: 17
source: dbSNP
start: 73383137
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs949071935
seq_region_name: 17
source: dbSNP
start: 73383138
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs183884807
seq_region_name: 17
source: dbSNP
start: 73383139
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs879041487
seq_region_name: 17
source: dbSNP
start: 73383140
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062845090
seq_region_name: 17
source: dbSNP
start: 73383143
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1042060273
seq_region_name: 17
source: dbSNP
start: 73383151
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062845108
seq_region_name: 17
source: dbSNP
start: 73383154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1819961714
seq_region_name: 17
source: dbSNP
start: 73383155
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs892764167
seq_region_name: 17
source: dbSNP
start: 73383156
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599505694
seq_region_name: 17
source: dbSNP
start: 73383160
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs547599801
seq_region_name: 17
source: dbSNP
start: 73383163
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1462475386
seq_region_name: 17
source: dbSNP
start: 73383164
strand: 1
-
alleles:
- AA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383165
feature_type: variation
id: rs1401211531
seq_region_name: 17
source: dbSNP
start: 73383164
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1011119399
seq_region_name: 17
source: dbSNP
start: 73383167
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383170
feature_type: variation
id: rs2062845230
seq_region_name: 17
source: dbSNP
start: 73383170
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs370877787
seq_region_name: 17
source: dbSNP
start: 73383172
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062845269
seq_region_name: 17
source: dbSNP
start: 73383174
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062845286
seq_region_name: 17
source: dbSNP
start: 73383175
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs902396152
seq_region_name: 17
source: dbSNP
start: 73383176
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1432673917
seq_region_name: 17
source: dbSNP
start: 73383178
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383181
feature_type: variation
id: rs565525383
seq_region_name: 17
source: dbSNP
start: 73383181
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565791144
seq_region_name: 17
source: dbSNP
start: 73383182
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383188
feature_type: variation
id: rs536254380
seq_region_name: 17
source: dbSNP
start: 73383188
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383189
feature_type: variation
id: rs2062845382
seq_region_name: 17
source: dbSNP
start: 73383189
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383190
feature_type: variation
id: rs1238008120
seq_region_name: 17
source: dbSNP
start: 73383190
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383192
feature_type: variation
id: rs889598730
seq_region_name: 17
source: dbSNP
start: 73383192
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383194
feature_type: variation
id: rs73345938
seq_region_name: 17
source: dbSNP
start: 73383194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383207
feature_type: variation
id: rs1568374958
seq_region_name: 17
source: dbSNP
start: 73383207
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383208
feature_type: variation
id: rs1599505767
seq_region_name: 17
source: dbSNP
start: 73383208
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383211
feature_type: variation
id: rs2062845517
seq_region_name: 17
source: dbSNP
start: 73383211
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383213
feature_type: variation
id: rs1254772581
seq_region_name: 17
source: dbSNP
start: 73383213
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383214
feature_type: variation
id: rs2062845565
seq_region_name: 17
source: dbSNP
start: 73383214
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383216
feature_type: variation
id: rs575975607
seq_region_name: 17
source: dbSNP
start: 73383216
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383217
feature_type: variation
id: rs2062845647
seq_region_name: 17
source: dbSNP
start: 73383217
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383220
feature_type: variation
id: rs1230364955
seq_region_name: 17
source: dbSNP
start: 73383220
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383221
feature_type: variation
id: rs1599505775
seq_region_name: 17
source: dbSNP
start: 73383221
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383223
feature_type: variation
id: rs2062845702
seq_region_name: 17
source: dbSNP
start: 73383223
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383225
feature_type: variation
id: rs148576899
seq_region_name: 17
source: dbSNP
start: 73383225
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383227
feature_type: variation
id: rs1242211374
seq_region_name: 17
source: dbSNP
start: 73383227
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383232
feature_type: variation
id: rs2062845821
seq_region_name: 17
source: dbSNP
start: 73383232
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383233
feature_type: variation
id: rs2062845856
seq_region_name: 17
source: dbSNP
start: 73383233
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383234
feature_type: variation
id: rs2062845885
seq_region_name: 17
source: dbSNP
start: 73383234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383237
feature_type: variation
id: rs2062845921
seq_region_name: 17
source: dbSNP
start: 73383237
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383239
feature_type: variation
id: rs2062845960
seq_region_name: 17
source: dbSNP
start: 73383239
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383242
feature_type: variation
id: rs901296299
seq_region_name: 17
source: dbSNP
start: 73383242
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383245
feature_type: variation
id: rs2145478385
seq_region_name: 17
source: dbSNP
start: 73383245
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383246
feature_type: variation
id: rs2062846026
seq_region_name: 17
source: dbSNP
start: 73383246
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383247
feature_type: variation
id: rs2145478397
seq_region_name: 17
source: dbSNP
start: 73383247
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383249
feature_type: variation
id: rs1236093025
seq_region_name: 17
source: dbSNP
start: 73383248
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383254
feature_type: variation
id: rs1599505806
seq_region_name: 17
source: dbSNP
start: 73383254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383262
feature_type: variation
id: rs2145478417
seq_region_name: 17
source: dbSNP
start: 73383262
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383265
feature_type: variation
id: rs1374352959
seq_region_name: 17
source: dbSNP
start: 73383265
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383267
feature_type: variation
id: rs994534460
seq_region_name: 17
source: dbSNP
start: 73383267
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383269
feature_type: variation
id: rs1025650361
seq_region_name: 17
source: dbSNP
start: 73383269
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383270
feature_type: variation
id: rs576977930
seq_region_name: 17
source: dbSNP
start: 73383270
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383277
feature_type: variation
id: rs2062846310
seq_region_name: 17
source: dbSNP
start: 73383277
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383281
feature_type: variation
id: rs953046787
seq_region_name: 17
source: dbSNP
start: 73383281
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383282
feature_type: variation
id: rs2062846376
seq_region_name: 17
source: dbSNP
start: 73383282
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383283
feature_type: variation
id: rs114859380
seq_region_name: 17
source: dbSNP
start: 73383283
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383284
feature_type: variation
id: rs142515554
seq_region_name: 17
source: dbSNP
start: 73383284
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383291
feature_type: variation
id: rs2062846517
seq_region_name: 17
source: dbSNP
start: 73383291
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383292
feature_type: variation
id: rs924395756
seq_region_name: 17
source: dbSNP
start: 73383292
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383293
feature_type: variation
id: rs958855381
seq_region_name: 17
source: dbSNP
start: 73383293
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383295
feature_type: variation
id: rs574575228
seq_region_name: 17
source: dbSNP
start: 73383295
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383300
feature_type: variation
id: rs541893196
seq_region_name: 17
source: dbSNP
start: 73383300
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383301
feature_type: variation
id: rs2062846680
seq_region_name: 17
source: dbSNP
start: 73383301
strand: 1
-
alleles:
- GGCTCTCCCTGACATTTCCACCTGGGCTC
- GGCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383329
feature_type: variation
id: rs2062846709
seq_region_name: 17
source: dbSNP
start: 73383301
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383305
feature_type: variation
id: rs2145478511
seq_region_name: 17
source: dbSNP
start: 73383305
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383306
feature_type: variation
id: rs2062846742
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383414
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383415
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383416
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383418
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1187833998
seq_region_name: 17
source: dbSNP
start: 73383419
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383425
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73383428
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383436
strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2062848223
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs749219156
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383443
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383447
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs901218209
seq_region_name: 17
source: dbSNP
start: 73383448
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383450
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383452
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383453
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1047480846
seq_region_name: 17
source: dbSNP
start: 73383465
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383469
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383472
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1335989836
seq_region_name: 17
source: dbSNP
start: 73383473
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383475
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1398175793
seq_region_name: 17
source: dbSNP
start: 73383476
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs888433899
seq_region_name: 17
source: dbSNP
start: 73383478
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs951494654
seq_region_name: 17
source: dbSNP
start: 73383483
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1319194285
seq_region_name: 17
source: dbSNP
start: 73383484
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383495
feature_type: variation
id: rs1005582946
seq_region_name: 17
source: dbSNP
start: 73383495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383499
feature_type: variation
id: rs1599506027
seq_region_name: 17
source: dbSNP
start: 73383499
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383505
feature_type: variation
id: rs1389009585
seq_region_name: 17
source: dbSNP
start: 73383505
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383506
feature_type: variation
id: rs2062848685
seq_region_name: 17
source: dbSNP
start: 73383506
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383508
feature_type: variation
id: rs1004315866
seq_region_name: 17
source: dbSNP
start: 73383508
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383510
feature_type: variation
id: rs1034600988
seq_region_name: 17
source: dbSNP
start: 73383510
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383515
feature_type: variation
id: rs1599506038
seq_region_name: 17
source: dbSNP
start: 73383515
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383519
feature_type: variation
id: rs1290617701
seq_region_name: 17
source: dbSNP
start: 73383519
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383520
feature_type: variation
id: rs1462296920
seq_region_name: 17
source: dbSNP
start: 73383520
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383523
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383523
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383526
feature_type: variation
id: rs2062848818
seq_region_name: 17
source: dbSNP
start: 73383526
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383527
feature_type: variation
id: rs373743512
seq_region_name: 17
source: dbSNP
start: 73383527
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73383697
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73383702
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73383705
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383710
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383711
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73383717
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73383718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383719
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383720
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383721
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73383723
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383725
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383728
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383742
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383743
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383746
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383755
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383756
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383759
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383760
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73383762
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs887293824
seq_region_name: 17
source: dbSNP
start: 73383765
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383767
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383770
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383771
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383772
strand: 1
-
alleles:
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- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383775
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73383773
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383778
feature_type: variation
id: rs1281750785
seq_region_name: 17
source: dbSNP
start: 73383778
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1446527178
seq_region_name: 17
source: dbSNP
start: 73383779
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383785
feature_type: variation
id: rs2062850536
seq_region_name: 17
source: dbSNP
start: 73383785
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383786
feature_type: variation
id: rs1599506314
seq_region_name: 17
source: dbSNP
start: 73383786
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383788
feature_type: variation
id: rs2062850576
seq_region_name: 17
source: dbSNP
start: 73383788
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs894702854
seq_region_name: 17
source: dbSNP
start: 73383795
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062850618
seq_region_name: 17
source: dbSNP
start: 73383800
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062850646
seq_region_name: 17
source: dbSNP
start: 73383801
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1353008753
seq_region_name: 17
source: dbSNP
start: 73383802
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1014533936
seq_region_name: 17
source: dbSNP
start: 73383805
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383814
feature_type: variation
id: rs560216538
seq_region_name: 17
source: dbSNP
start: 73383814
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs563339800
seq_region_name: 17
source: dbSNP
start: 73383815
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs575154653
seq_region_name: 17
source: dbSNP
start: 73383821
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383826
feature_type: variation
id: rs1459005997
seq_region_name: 17
source: dbSNP
start: 73383826
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1196700035
seq_region_name: 17
source: dbSNP
start: 73383830
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383831
feature_type: variation
id: rs2062850811
seq_region_name: 17
source: dbSNP
start: 73383831
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs140290310
seq_region_name: 17
source: dbSNP
start: 73383832
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383833
feature_type: variation
id: rs200993992
seq_region_name: 17
source: dbSNP
start: 73383833
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383834
feature_type: variation
id: rs770945306
seq_region_name: 17
source: dbSNP
start: 73383834
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383836
feature_type: variation
id: rs1030747472
seq_region_name: 17
source: dbSNP
start: 73383836
strand: 1
-
alleles:
- CCCATCCCACCCAT
- CCCAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383849
feature_type: variation
id: rs2062850904
seq_region_name: 17
source: dbSNP
start: 73383836
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383838
feature_type: variation
id: rs779979198
seq_region_name: 17
source: dbSNP
start: 73383838
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383842
feature_type: variation
id: rs2062850948
seq_region_name: 17
source: dbSNP
start: 73383842
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383843
feature_type: variation
id: rs1422884185
seq_region_name: 17
source: dbSNP
start: 73383843
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383845
feature_type: variation
id: rs747174910
seq_region_name: 17
source: dbSNP
start: 73383845
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383846
feature_type: variation
id: rs1425176399
seq_region_name: 17
source: dbSNP
start: 73383846
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383847
feature_type: variation
id: rs1463649316
seq_region_name: 17
source: dbSNP
start: 73383847
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383848
feature_type: variation
id: rs369209011
seq_region_name: 17
source: dbSNP
start: 73383848
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383849
feature_type: variation
id: rs2062851076
seq_region_name: 17
source: dbSNP
start: 73383849
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383850
feature_type: variation
id: rs762829089
seq_region_name: 17
source: dbSNP
start: 73383849
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383852
feature_type: variation
id: rs768997441
seq_region_name: 17
source: dbSNP
start: 73383852
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383853
feature_type: variation
id: rs777003711
seq_region_name: 17
source: dbSNP
start: 73383853
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383855
feature_type: variation
id: rs957786314
seq_region_name: 17
source: dbSNP
start: 73383855
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383858
feature_type: variation
id: rs1166082278
seq_region_name: 17
source: dbSNP
start: 73383858
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383859
feature_type: variation
id: rs746769118
seq_region_name: 17
source: dbSNP
start: 73383859
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383860
feature_type: variation
id: rs2062851237
seq_region_name: 17
source: dbSNP
start: 73383860
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383862
feature_type: variation
id: rs766032743
seq_region_name: 17
source: dbSNP
start: 73383860
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383862
feature_type: variation
id: rs1453821175
seq_region_name: 17
source: dbSNP
start: 73383862
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383863
feature_type: variation
id: rs770310051
seq_region_name: 17
source: dbSNP
start: 73383863
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383865
feature_type: variation
id: rs773662493
seq_region_name: 17
source: dbSNP
start: 73383865
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73383867
feature_type: variation
id: rs1599506418
seq_region_name: 17
source: dbSNP
start: 73383867
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73383873
feature_type: variation
id: rs963903201
seq_region_name: 17
source: dbSNP
start: 73383873
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383878
feature_type: variation
id: rs757185853
seq_region_name: 17
source: dbSNP
start: 73383878
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383883
feature_type: variation
id: rs763345868
seq_region_name: 17
source: dbSNP
start: 73383883
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383887
feature_type: variation
id: rs35171980
seq_region_name: 17
source: dbSNP
start: 73383887
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383889
feature_type: variation
id: rs2145479757
seq_region_name: 17
source: dbSNP
start: 73383889
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383891
feature_type: variation
id: rs766966307
seq_region_name: 17
source: dbSNP
start: 73383891
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383892
feature_type: variation
id: rs773727796
seq_region_name: 17
source: dbSNP
start: 73383892
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383896
feature_type: variation
id: rs1257327552
seq_region_name: 17
source: dbSNP
start: 73383896
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383897
feature_type: variation
id: rs2062851548
seq_region_name: 17
source: dbSNP
start: 73383897
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383900
feature_type: variation
id: rs1324199488
seq_region_name: 17
source: dbSNP
start: 73383900
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383902
feature_type: variation
id: rs1215389855
seq_region_name: 17
source: dbSNP
start: 73383902
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383904
feature_type: variation
id: rs759049279
seq_region_name: 17
source: dbSNP
start: 73383904
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383907
feature_type: variation
id: rs976677346
seq_region_name: 17
source: dbSNP
start: 73383907
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383908
feature_type: variation
id: rs2145479808
seq_region_name: 17
source: dbSNP
start: 73383908
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73383910
feature_type: variation
id: rs150173502
seq_region_name: 17
source: dbSNP
start: 73383910
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383912
feature_type: variation
id: rs2062851765
seq_region_name: 17
source: dbSNP
start: 73383912
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383917
feature_type: variation
id: rs532828854
seq_region_name: 17
source: dbSNP
start: 73383917
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383921
feature_type: variation
id: rs1264930292
seq_region_name: 17
source: dbSNP
start: 73383921
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383922
feature_type: variation
id: rs755863605
seq_region_name: 17
source: dbSNP
start: 73383922
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383923
feature_type: variation
id: rs35467001
seq_region_name: 17
source: dbSNP
start: 73383923
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383928
feature_type: variation
id: rs753718657
seq_region_name: 17
source: dbSNP
start: 73383928
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383929
feature_type: variation
id: rs971769002
seq_region_name: 17
source: dbSNP
start: 73383929
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383930
feature_type: variation
id: rs757131822
seq_region_name: 17
source: dbSNP
start: 73383930
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383932
feature_type: variation
id: rs778978606
seq_region_name: 17
source: dbSNP
start: 73383932
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383937
feature_type: variation
id: rs1357811997
seq_region_name: 17
source: dbSNP
start: 73383937
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383938
feature_type: variation
id: rs373967562
seq_region_name: 17
source: dbSNP
start: 73383938
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383940
feature_type: variation
id: rs2062852089
seq_region_name: 17
source: dbSNP
start: 73383940
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383944
feature_type: variation
id: rs755128556
seq_region_name: 17
source: dbSNP
start: 73383944
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383946
feature_type: variation
id: rs2062852142
seq_region_name: 17
source: dbSNP
start: 73383946
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383948
feature_type: variation
id: rs2270716
seq_region_name: 17
source: dbSNP
start: 73383948
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383950
feature_type: variation
id: rs1055782501
seq_region_name: 17
source: dbSNP
start: 73383950
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383951
feature_type: variation
id: rs12952305
seq_region_name: 17
source: dbSNP
start: 73383951
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383953
feature_type: variation
id: rs1398160253
seq_region_name: 17
source: dbSNP
start: 73383953
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383954
feature_type: variation
id: rs530166844
seq_region_name: 17
source: dbSNP
start: 73383954
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383955
feature_type: variation
id: rs2062852333
seq_region_name: 17
source: dbSNP
start: 73383955
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383956
feature_type: variation
id: rs374738523
seq_region_name: 17
source: dbSNP
start: 73383956
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73383957
feature_type: variation
id: rs773435219
seq_region_name: 17
source: dbSNP
start: 73383957
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73383960
feature_type: variation
id: rs377639571
seq_region_name: 17
source: dbSNP
start: 73383960
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383962
feature_type: variation
id: rs771273833
seq_region_name: 17
source: dbSNP
start: 73383962
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383963
feature_type: variation
id: rs2062852466
seq_region_name: 17
source: dbSNP
start: 73383963
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383964
feature_type: variation
id: rs2062852503
seq_region_name: 17
source: dbSNP
start: 73383964
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73383968
feature_type: variation
id: rs146088947
seq_region_name: 17
source: dbSNP
start: 73383968
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73383969
feature_type: variation
id: rs199630308
seq_region_name: 17
source: dbSNP
start: 73383969
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383973
feature_type: variation
id: rs2062852593
seq_region_name: 17
source: dbSNP
start: 73383973
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383979
feature_type: variation
id: rs1487112225
seq_region_name: 17
source: dbSNP
start: 73383979
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383981
feature_type: variation
id: rs767046719
seq_region_name: 17
source: dbSNP
start: 73383981
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383991
feature_type: variation
id: rs2062852668
seq_region_name: 17
source: dbSNP
start: 73383991
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383992
feature_type: variation
id: rs2062852681
seq_region_name: 17
source: dbSNP
start: 73383992
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383994
feature_type: variation
id: rs2062852706
seq_region_name: 17
source: dbSNP
start: 73383994
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383995
feature_type: variation
id: rs111968107
seq_region_name: 17
source: dbSNP
start: 73383995
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73383997
feature_type: variation
id: rs2062852749
seq_region_name: 17
source: dbSNP
start: 73383997
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73383999
feature_type: variation
id: rs775021565
seq_region_name: 17
source: dbSNP
start: 73383999
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73384005
feature_type: variation
id: rs2062852798
seq_region_name: 17
source: dbSNP
start: 73384005
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73384009
feature_type: variation
id: rs760302351
seq_region_name: 17
source: dbSNP
start: 73384009
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73384010
feature_type: variation
id: rs763869312
seq_region_name: 17
source: dbSNP
start: 73384010
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73384012
feature_type: variation
id: rs2145480108
seq_region_name: 17
source: dbSNP
start: 73384012
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73384014
feature_type: variation
id: rs1423736095
seq_region_name: 17
source: dbSNP
start: 73384014
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73384015
feature_type: variation
id: rs753573465
seq_region_name: 17
source: dbSNP
start: 73384015
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73384016
feature_type: variation
id: rs2062852888
seq_region_name: 17
source: dbSNP
start: 73384016
strand: 1
-
alleles:
- AGGAAGG
- AGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73384022
feature_type: variation
id: rs2062852920
seq_region_name: 17
source: dbSNP
start: 73384016
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73384017
feature_type: variation
id: rs1259803329
seq_region_name: 17
source: dbSNP
start: 73384017
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73384022
feature_type: variation
id: rs192497165
seq_region_name: 17
source: dbSNP
start: 73384022
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73384025
feature_type: variation
id: rs765033830
seq_region_name: 17
source: dbSNP
start: 73384025
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73384026
feature_type: variation
id: rs750415571
seq_region_name: 17
source: dbSNP
start: 73384026
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73384028
feature_type: variation
id: rs758447468
seq_region_name: 17
source: dbSNP
start: 73384028
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384030
feature_type: variation
id: rs1297603028
seq_region_name: 17
source: dbSNP
start: 73384030
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384033
feature_type: variation
id: rs1350519223
seq_region_name: 17
source: dbSNP
start: 73384033
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384035
feature_type: variation
id: rs1438749733
seq_region_name: 17
source: dbSNP
start: 73384035
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384041
feature_type: variation
id: rs1486354811
seq_region_name: 17
source: dbSNP
start: 73384041
strand: 1
-
alleles:
- "-"
- GTGGGTGGTGGTCCAGGTGCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384041
feature_type: variation
id: rs1568375321
seq_region_name: 17
source: dbSNP
start: 73384042
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384042
feature_type: variation
id: rs77844675
seq_region_name: 17
source: dbSNP
start: 73384042
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384044
feature_type: variation
id: rs1334636090
seq_region_name: 17
source: dbSNP
start: 73384044
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384051
feature_type: variation
id: rs748296179
seq_region_name: 17
source: dbSNP
start: 73384051
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384056
feature_type: variation
id: rs76207297
seq_region_name: 17
source: dbSNP
start: 73384056
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384057
feature_type: variation
id: rs749555855
seq_region_name: 17
source: dbSNP
start: 73384057
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384059
feature_type: variation
id: rs1599506704
seq_region_name: 17
source: dbSNP
start: 73384059
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384060
feature_type: variation
id: rs372060531
seq_region_name: 17
source: dbSNP
start: 73384060
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384063
feature_type: variation
id: rs570704464
seq_region_name: 17
source: dbSNP
start: 73384063
strand: 1
-
alleles:
- CCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384068
feature_type: variation
id: rs2062853313
seq_region_name: 17
source: dbSNP
start: 73384065
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384066
feature_type: variation
id: rs1051376908
seq_region_name: 17
source: dbSNP
start: 73384066
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384067
feature_type: variation
id: rs976856593
seq_region_name: 17
source: dbSNP
start: 73384067
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384070
feature_type: variation
id: rs1029543880
seq_region_name: 17
source: dbSNP
start: 73384070
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384071
feature_type: variation
id: rs951384762
seq_region_name: 17
source: dbSNP
start: 73384071
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384074
feature_type: variation
id: rs2062853442
seq_region_name: 17
source: dbSNP
start: 73384074
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384076
feature_type: variation
id: rs1362153984
seq_region_name: 17
source: dbSNP
start: 73384076
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384078
feature_type: variation
id: rs775800378
seq_region_name: 17
source: dbSNP
start: 73384078
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384079
feature_type: variation
id: rs2062853511
seq_region_name: 17
source: dbSNP
start: 73384079
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384081
feature_type: variation
id: rs2062853539
seq_region_name: 17
source: dbSNP
start: 73384081
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384085
feature_type: variation
id: rs747359666
seq_region_name: 17
source: dbSNP
start: 73384085
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384087
feature_type: variation
id: rs1326473314
seq_region_name: 17
source: dbSNP
start: 73384087
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384089
feature_type: variation
id: rs2062853613
seq_region_name: 17
source: dbSNP
start: 73384089
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384092
feature_type: variation
id: rs1463003434
seq_region_name: 17
source: dbSNP
start: 73384092
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384093
feature_type: variation
id: rs1599506764
seq_region_name: 17
source: dbSNP
start: 73384093
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384096
feature_type: variation
id: rs2062853680
seq_region_name: 17
source: dbSNP
start: 73384096
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384102
feature_type: variation
id: rs2062853704
seq_region_name: 17
source: dbSNP
start: 73384102
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384104
feature_type: variation
id: rs769019025
seq_region_name: 17
source: dbSNP
start: 73384104
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384105
feature_type: variation
id: rs941198599
seq_region_name: 17
source: dbSNP
start: 73384105
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384106
feature_type: variation
id: rs1366094230
seq_region_name: 17
source: dbSNP
start: 73384106
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384119
feature_type: variation
id: rs1230715211
seq_region_name: 17
source: dbSNP
start: 73384119
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384121
feature_type: variation
id: rs1429212384
seq_region_name: 17
source: dbSNP
start: 73384121
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384122
feature_type: variation
id: rs2062853824
seq_region_name: 17
source: dbSNP
start: 73384122
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384129
feature_type: variation
id: rs2270717
seq_region_name: 17
source: dbSNP
start: 73384129
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384137
feature_type: variation
id: rs916033143
seq_region_name: 17
source: dbSNP
start: 73384137
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384139
feature_type: variation
id: rs2062853899
seq_region_name: 17
source: dbSNP
start: 73384139
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384144
feature_type: variation
id: rs1221962219
seq_region_name: 17
source: dbSNP
start: 73384144
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384145
feature_type: variation
id: rs1254069232
seq_region_name: 17
source: dbSNP
start: 73384145
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384147
feature_type: variation
id: rs2062854007
seq_region_name: 17
source: dbSNP
start: 73384147
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384152
feature_type: variation
id: rs2062854042
seq_region_name: 17
source: dbSNP
start: 73384152
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384153
feature_type: variation
id: rs1216080128
seq_region_name: 17
source: dbSNP
start: 73384153
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384160
feature_type: variation
id: rs1479980691
seq_region_name: 17
source: dbSNP
start: 73384160
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384167
feature_type: variation
id: rs2062854126
seq_region_name: 17
source: dbSNP
start: 73384167
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384168
feature_type: variation
id: rs2062854161
seq_region_name: 17
source: dbSNP
start: 73384168
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384175
feature_type: variation
id: rs2062854196
seq_region_name: 17
source: dbSNP
start: 73384175
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384179
feature_type: variation
id: rs1267049845
seq_region_name: 17
source: dbSNP
start: 73384179
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384181
feature_type: variation
id: rs2062854272
seq_region_name: 17
source: dbSNP
start: 73384181
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384182
feature_type: variation
id: rs2062854320
seq_region_name: 17
source: dbSNP
start: 73384182
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384187
feature_type: variation
id: rs2062854354
seq_region_name: 17
source: dbSNP
start: 73384187
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384188
feature_type: variation
id: rs2062854395
seq_region_name: 17
source: dbSNP
start: 73384188
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384190
feature_type: variation
id: rs2145480428
seq_region_name: 17
source: dbSNP
start: 73384190
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384192
feature_type: variation
id: rs1251260234
seq_region_name: 17
source: dbSNP
start: 73384192
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384195
feature_type: variation
id: rs1226000607
seq_region_name: 17
source: dbSNP
start: 73384195
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384197
feature_type: variation
id: rs1307607511
seq_region_name: 17
source: dbSNP
start: 73384197
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384200
feature_type: variation
id: rs1299321448
seq_region_name: 17
source: dbSNP
start: 73384200
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384202
feature_type: variation
id: rs1487449002
seq_region_name: 17
source: dbSNP
start: 73384202
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384203
feature_type: variation
id: rs950078779
seq_region_name: 17
source: dbSNP
start: 73384203
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384207
feature_type: variation
id: rs2062854602
seq_region_name: 17
source: dbSNP
start: 73384207
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384208
feature_type: variation
id: rs2062854622
seq_region_name: 17
source: dbSNP
start: 73384208
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384209
feature_type: variation
id: rs1231686799
seq_region_name: 17
source: dbSNP
start: 73384209
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384212
feature_type: variation
id: rs1369962054
seq_region_name: 17
source: dbSNP
start: 73384212
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384214
feature_type: variation
id: rs1209240504
seq_region_name: 17
source: dbSNP
start: 73384214
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384215
feature_type: variation
id: rs2062854720
seq_region_name: 17
source: dbSNP
start: 73384215
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384217
feature_type: variation
id: rs1248094524
seq_region_name: 17
source: dbSNP
start: 73384217
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384228
feature_type: variation
id: rs2062854771
seq_region_name: 17
source: dbSNP
start: 73384228
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384232
feature_type: variation
id: rs1450732615
seq_region_name: 17
source: dbSNP
start: 73384232
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73384356
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384384
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384388
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384389
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384401
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384403
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384408
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384409
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384410
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384411
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384421
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384425
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384428
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384429
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384431
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384434
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384438
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384439
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1483370399
seq_region_name: 17
source: dbSNP
start: 73384440
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384441
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384442
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384446
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384447
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384448
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs577493182
seq_region_name: 17
source: dbSNP
start: 73384449
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599507039
seq_region_name: 17
source: dbSNP
start: 73384457
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384458
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384461
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384462
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384462
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384464
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73384469
feature_type: variation
id: rs2062856521
seq_region_name: 17
source: dbSNP
start: 73384469
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384471
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384472
feature_type: variation
id: rs2145480989
seq_region_name: 17
source: dbSNP
start: 73384472
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384476
feature_type: variation
id: rs1422360829
seq_region_name: 17
source: dbSNP
start: 73384476
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384477
feature_type: variation
id: rs2062856582
seq_region_name: 17
source: dbSNP
start: 73384477
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73384675
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384679
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73384680
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384683
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384692
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384697
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384698
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384700
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384702
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384703
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384705
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384707
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384708
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs954611417
seq_region_name: 17
source: dbSNP
start: 73384709
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1187647125
seq_region_name: 17
source: dbSNP
start: 73384717
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs541971576
seq_region_name: 17
source: dbSNP
start: 73384719
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568375522
seq_region_name: 17
source: dbSNP
start: 73384724
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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id: rs907546284
seq_region_name: 17
source: dbSNP
start: 73384726
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1291955351
seq_region_name: 17
source: dbSNP
start: 73384727
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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id: rs766434864
seq_region_name: 17
source: dbSNP
start: 73384730
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384731
feature_type: variation
id: rs77208238
seq_region_name: 17
source: dbSNP
start: 73384731
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384733
feature_type: variation
id: rs2062858373
seq_region_name: 17
source: dbSNP
start: 73384733
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384734
feature_type: variation
id: rs1473857847
seq_region_name: 17
source: dbSNP
start: 73384734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384737
feature_type: variation
id: rs1230950774
seq_region_name: 17
source: dbSNP
start: 73384736
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384739
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id: rs67818535
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2062858859
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1053097387
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs956224117
seq_region_name: 17
source: dbSNP
start: 73384801
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384808
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384809
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384812
strand: 1
-
alleles:
- CAAAACAAAACAAAACAAAA
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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source: dbSNP
start: 73384835
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73384840
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73384840
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384841
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73384848
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1334660286
seq_region_name: 17
source: dbSNP
start: 73384857
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384860
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384861
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384863
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2145481770
seq_region_name: 17
source: dbSNP
start: 73384864
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384865
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73384866
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1308049613
seq_region_name: 17
source: dbSNP
start: 73384870
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2145481788
seq_region_name: 17
source: dbSNP
start: 73384871
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs6501628
seq_region_name: 17
source: dbSNP
start: 73384872
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145481813
seq_region_name: 17
source: dbSNP
start: 73384874
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1373190574
seq_region_name: 17
source: dbSNP
start: 73384875
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062859571
seq_region_name: 17
source: dbSNP
start: 73384876
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1172661515
seq_region_name: 17
source: dbSNP
start: 73384878
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062859631
seq_region_name: 17
source: dbSNP
start: 73384883
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1352163213
seq_region_name: 17
source: dbSNP
start: 73384885
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062859678
seq_region_name: 17
source: dbSNP
start: 73384886
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062859699
seq_region_name: 17
source: dbSNP
start: 73384890
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1599507407
seq_region_name: 17
source: dbSNP
start: 73384894
strand: 1
-
alleles:
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- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs377102757
seq_region_name: 17
source: dbSNP
start: 73384895
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1427062431
seq_region_name: 17
source: dbSNP
start: 73384897
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs974860092
seq_region_name: 17
source: dbSNP
start: 73384898
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384899
feature_type: variation
id: rs78884401
seq_region_name: 17
source: dbSNP
start: 73384899
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599507425
seq_region_name: 17
source: dbSNP
start: 73384906
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062859858
seq_region_name: 17
source: dbSNP
start: 73384908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384910
feature_type: variation
id: rs2062859886
seq_region_name: 17
source: dbSNP
start: 73384910
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384911
feature_type: variation
id: rs933534784
seq_region_name: 17
source: dbSNP
start: 73384911
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384912
feature_type: variation
id: rs1599507435
seq_region_name: 17
source: dbSNP
start: 73384912
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384913
feature_type: variation
id: rs1051279859
seq_region_name: 17
source: dbSNP
start: 73384913
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384916
feature_type: variation
id: rs2062859964
seq_region_name: 17
source: dbSNP
start: 73384916
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384917
feature_type: variation
id: rs2145481900
seq_region_name: 17
source: dbSNP
start: 73384917
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384919
feature_type: variation
id: rs115311941
seq_region_name: 17
source: dbSNP
start: 73384919
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384921
feature_type: variation
id: rs2062860014
seq_region_name: 17
source: dbSNP
start: 73384921
strand: 1
-
alleles:
- CCCCC
- CCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384925
feature_type: variation
id: rs2062860036
seq_region_name: 17
source: dbSNP
start: 73384921
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384922
feature_type: variation
id: rs535657996
seq_region_name: 17
source: dbSNP
start: 73384922
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384924
feature_type: variation
id: rs1038050690
seq_region_name: 17
source: dbSNP
start: 73384924
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73384925
feature_type: variation
id: rs1257024191
seq_region_name: 17
source: dbSNP
start: 73384925
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73385036
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385037
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73385045
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385054
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385055
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385061
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385062
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385064
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73385066
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385068
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385070
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385071
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385072
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385076
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1014710298
seq_region_name: 17
source: dbSNP
start: 73385077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385079
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385084
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1438568551
seq_region_name: 17
source: dbSNP
start: 73385089
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385094
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs376160278
seq_region_name: 17
source: dbSNP
start: 73385095
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385097
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385098
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1468374578
seq_region_name: 17
source: dbSNP
start: 73385099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs898908252
seq_region_name: 17
source: dbSNP
start: 73385102
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs191665483
seq_region_name: 17
source: dbSNP
start: 73385104
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1272566026
seq_region_name: 17
source: dbSNP
start: 73385106
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062861792
seq_region_name: 17
source: dbSNP
start: 73385108
strand: 1
-
alleles:
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- GTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385122
feature_type: variation
id: rs2062861818
seq_region_name: 17
source: dbSNP
start: 73385117
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1221597043
seq_region_name: 17
source: dbSNP
start: 73385119
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568375698
seq_region_name: 17
source: dbSNP
start: 73385121
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385122
feature_type: variation
id: rs2145482403
seq_region_name: 17
source: dbSNP
start: 73385122
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385126
feature_type: variation
id: rs1038017780
seq_region_name: 17
source: dbSNP
start: 73385126
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062861909
seq_region_name: 17
source: dbSNP
start: 73385129
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062861931
seq_region_name: 17
source: dbSNP
start: 73385135
strand: 1
-
alleles:
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- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1292957056
seq_region_name: 17
source: dbSNP
start: 73385145
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1227275539
seq_region_name: 17
source: dbSNP
start: 73385151
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385153
feature_type: variation
id: rs1365659415
seq_region_name: 17
source: dbSNP
start: 73385153
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385160
feature_type: variation
id: rs2062862019
seq_region_name: 17
source: dbSNP
start: 73385160
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385161
feature_type: variation
id: rs2062862052
seq_region_name: 17
source: dbSNP
start: 73385161
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385162
feature_type: variation
id: rs2062862077
seq_region_name: 17
source: dbSNP
start: 73385162
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385166
feature_type: variation
id: rs2062862103
seq_region_name: 17
source: dbSNP
start: 73385166
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385170
feature_type: variation
id: rs2062862126
seq_region_name: 17
source: dbSNP
start: 73385170
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385173
feature_type: variation
id: rs553254010
seq_region_name: 17
source: dbSNP
start: 73385173
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385175
feature_type: variation
id: rs574750428
seq_region_name: 17
source: dbSNP
start: 73385175
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385177
feature_type: variation
id: rs2062862199
seq_region_name: 17
source: dbSNP
start: 73385177
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385179
feature_type: variation
id: rs898144906
seq_region_name: 17
source: dbSNP
start: 73385179
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385184
feature_type: variation
id: rs1023722889
seq_region_name: 17
source: dbSNP
start: 73385184
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385186
feature_type: variation
id: rs2062862261
seq_region_name: 17
source: dbSNP
start: 73385186
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385188
feature_type: variation
id: rs534893847
seq_region_name: 17
source: dbSNP
start: 73385186
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385187
feature_type: variation
id: rs76024578
seq_region_name: 17
source: dbSNP
start: 73385187
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385192
feature_type: variation
id: rs1044695133
seq_region_name: 17
source: dbSNP
start: 73385192
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385195
feature_type: variation
id: rs2062862365
seq_region_name: 17
source: dbSNP
start: 73385195
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385197
feature_type: variation
id: rs2062862386
seq_region_name: 17
source: dbSNP
start: 73385197
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385207
feature_type: variation
id: rs960227094
seq_region_name: 17
source: dbSNP
start: 73385207
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385216
feature_type: variation
id: rs2062862431
seq_region_name: 17
source: dbSNP
start: 73385216
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385219
feature_type: variation
id: rs2062862448
seq_region_name: 17
source: dbSNP
start: 73385219
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385221
feature_type: variation
id: rs2062862467
seq_region_name: 17
source: dbSNP
start: 73385221
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385224
feature_type: variation
id: rs1430714088
seq_region_name: 17
source: dbSNP
start: 73385224
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385230
feature_type: variation
id: rs1599507706
seq_region_name: 17
source: dbSNP
start: 73385230
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385232
feature_type: variation
id: rs1194388304
seq_region_name: 17
source: dbSNP
start: 73385232
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385233
feature_type: variation
id: rs74653295
seq_region_name: 17
source: dbSNP
start: 73385233
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385234
feature_type: variation
id: rs1800437732
seq_region_name: 17
source: dbSNP
start: 73385234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385235
feature_type: variation
id: rs1003078064
seq_region_name: 17
source: dbSNP
start: 73385235
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385236
feature_type: variation
id: rs377160223
seq_region_name: 17
source: dbSNP
start: 73385236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385237
feature_type: variation
id: rs891858981
seq_region_name: 17
source: dbSNP
start: 73385237
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385238
feature_type: variation
id: rs779337779
seq_region_name: 17
source: dbSNP
start: 73385238
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385239
feature_type: variation
id: rs2062862636
seq_region_name: 17
source: dbSNP
start: 73385239
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385241
feature_type: variation
id: rs2062862649
seq_region_name: 17
source: dbSNP
start: 73385241
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385242
feature_type: variation
id: rs2062862675
seq_region_name: 17
source: dbSNP
start: 73385242
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385243
feature_type: variation
id: rs2145482643
seq_region_name: 17
source: dbSNP
start: 73385243
strand: 1
-
alleles:
- AG
- AGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385244
feature_type: variation
id: rs1568375732
seq_region_name: 17
source: dbSNP
start: 73385243
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385245
feature_type: variation
id: rs2062862717
seq_region_name: 17
source: dbSNP
start: 73385245
strand: 1
-
alleles:
- CCCATGAGCAGCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385259
feature_type: variation
id: rs2062862750
seq_region_name: 17
source: dbSNP
start: 73385247
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385248
feature_type: variation
id: rs1468037411
seq_region_name: 17
source: dbSNP
start: 73385248
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385252
feature_type: variation
id: rs978834849
seq_region_name: 17
source: dbSNP
start: 73385252
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385254
feature_type: variation
id: rs1189330107
seq_region_name: 17
source: dbSNP
start: 73385254
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385256
feature_type: variation
id: rs921941554
seq_region_name: 17
source: dbSNP
start: 73385256
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385259
feature_type: variation
id: rs1021695820
seq_region_name: 17
source: dbSNP
start: 73385259
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385261
feature_type: variation
id: rs931979622
seq_region_name: 17
source: dbSNP
start: 73385261
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385263
feature_type: variation
id: rs2145482696
seq_region_name: 17
source: dbSNP
start: 73385263
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385264
feature_type: variation
id: rs546295659
seq_region_name: 17
source: dbSNP
start: 73385264
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385265
feature_type: variation
id: rs149924178
seq_region_name: 17
source: dbSNP
start: 73385265
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385268
feature_type: variation
id: rs890363666
seq_region_name: 17
source: dbSNP
start: 73385268
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385271
feature_type: variation
id: rs2062862986
seq_region_name: 17
source: dbSNP
start: 73385271
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385272
feature_type: variation
id: rs1327343098
seq_region_name: 17
source: dbSNP
start: 73385272
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385281
feature_type: variation
id: rs1371268368
seq_region_name: 17
source: dbSNP
start: 73385281
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385282
feature_type: variation
id: rs2145482738
seq_region_name: 17
source: dbSNP
start: 73385282
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385283
feature_type: variation
id: rs2145482745
seq_region_name: 17
source: dbSNP
start: 73385283
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385284
feature_type: variation
id: rs940538571
seq_region_name: 17
source: dbSNP
start: 73385284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385287
feature_type: variation
id: rs1407006993
seq_region_name: 17
source: dbSNP
start: 73385287
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385290
feature_type: variation
id: rs2145482767
seq_region_name: 17
source: dbSNP
start: 73385290
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385296
feature_type: variation
id: rs1321448147
seq_region_name: 17
source: dbSNP
start: 73385296
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385297
feature_type: variation
id: rs1331538874
seq_region_name: 17
source: dbSNP
start: 73385297
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385299
feature_type: variation
id: rs1036194831
seq_region_name: 17
source: dbSNP
start: 73385299
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385301
feature_type: variation
id: rs2145482791
seq_region_name: 17
source: dbSNP
start: 73385301
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385302
feature_type: variation
id: rs1172041113
seq_region_name: 17
source: dbSNP
start: 73385302
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385303
feature_type: variation
id: rs2062863182
seq_region_name: 17
source: dbSNP
start: 73385303
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385313
feature_type: variation
id: rs2062863201
seq_region_name: 17
source: dbSNP
start: 73385313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385315
feature_type: variation
id: rs1393652162
seq_region_name: 17
source: dbSNP
start: 73385315
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385318
feature_type: variation
id: rs898957516
seq_region_name: 17
source: dbSNP
start: 73385318
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385318
feature_type: variation
id: rs1465827228
seq_region_name: 17
source: dbSNP
start: 73385318
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385319
feature_type: variation
id: rs77470631
seq_region_name: 17
source: dbSNP
start: 73385319
strand: 1
-
alleles:
- AA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385322
feature_type: variation
id: rs2062863328
seq_region_name: 17
source: dbSNP
start: 73385321
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385322
feature_type: variation
id: rs2062863354
seq_region_name: 17
source: dbSNP
start: 73385322
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385325
feature_type: variation
id: rs1044789723
seq_region_name: 17
source: dbSNP
start: 73385325
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385326
feature_type: variation
id: rs1599507842
seq_region_name: 17
source: dbSNP
start: 73385326
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385327
feature_type: variation
id: rs954992988
seq_region_name: 17
source: dbSNP
start: 73385327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385330
feature_type: variation
id: rs1483115066
seq_region_name: 17
source: dbSNP
start: 73385330
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385332
feature_type: variation
id: rs1253492099
seq_region_name: 17
source: dbSNP
start: 73385332
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385333
feature_type: variation
id: rs2062863493
seq_region_name: 17
source: dbSNP
start: 73385333
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385340
feature_type: variation
id: rs2062863533
seq_region_name: 17
source: dbSNP
start: 73385340
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385341
feature_type: variation
id: rs983997722
seq_region_name: 17
source: dbSNP
start: 73385341
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385342
feature_type: variation
id: rs546977088
seq_region_name: 17
source: dbSNP
start: 73385342
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385343
feature_type: variation
id: rs1599507863
seq_region_name: 17
source: dbSNP
start: 73385343
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385345
feature_type: variation
id: rs1226290375
seq_region_name: 17
source: dbSNP
start: 73385345
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385348
feature_type: variation
id: rs2062863644
seq_region_name: 17
source: dbSNP
start: 73385348
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73385501
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385509
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385510
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73385511
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73385512
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385513
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73385516
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385517
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385521
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385530
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs574841489
seq_region_name: 17
source: dbSNP
start: 73385535
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385540
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385541
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385552
strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2062865121
seq_region_name: 17
source: dbSNP
start: 73385553
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73385554
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385556
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062865178
seq_region_name: 17
source: dbSNP
start: 73385557
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385562
feature_type: variation
id: rs1599508115
seq_region_name: 17
source: dbSNP
start: 73385562
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385563
feature_type: variation
id: rs1271222933
seq_region_name: 17
source: dbSNP
start: 73385563
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73385568
feature_type: variation
id: rs1030346669
seq_region_name: 17
source: dbSNP
start: 73385568
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73385575
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385576
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385579
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385579
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385580
feature_type: variation
id: rs955103948
seq_region_name: 17
source: dbSNP
start: 73385580
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385585
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1005116525
seq_region_name: 17
source: dbSNP
start: 73385592
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062865389
seq_region_name: 17
source: dbSNP
start: 73385593
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1010458269
seq_region_name: 17
source: dbSNP
start: 73385594
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1364920950
seq_region_name: 17
source: dbSNP
start: 73385598
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599508149
seq_region_name: 17
source: dbSNP
start: 73385602
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385603
feature_type: variation
id: rs1298714564
seq_region_name: 17
source: dbSNP
start: 73385603
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385604
feature_type: variation
id: rs2145483414
seq_region_name: 17
source: dbSNP
start: 73385604
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1020471334
seq_region_name: 17
source: dbSNP
start: 73385609
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385610
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73385610
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385613
feature_type: variation
id: rs767370104
seq_region_name: 17
source: dbSNP
start: 73385613
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385830
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385834
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385835
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73385836
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385837
feature_type: variation
id: rs750288871
seq_region_name: 17
source: dbSNP
start: 73385837
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385838
feature_type: variation
id: rs201608312
seq_region_name: 17
source: dbSNP
start: 73385838
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73385839
feature_type: variation
id: rs1284422967
seq_region_name: 17
source: dbSNP
start: 73385839
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73385842
feature_type: variation
id: rs2062867413
seq_region_name: 17
source: dbSNP
start: 73385842
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73385843
feature_type: variation
id: rs2145483994
seq_region_name: 17
source: dbSNP
start: 73385843
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73385846
feature_type: variation
id: rs1208715536
seq_region_name: 17
source: dbSNP
start: 73385846
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73385850
feature_type: variation
id: rs762970443
seq_region_name: 17
source: dbSNP
start: 73385850
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385853
feature_type: variation
id: rs1327864201
seq_region_name: 17
source: dbSNP
start: 73385853
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385854
feature_type: variation
id: rs766490350
seq_region_name: 17
source: dbSNP
start: 73385854
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73385855
feature_type: variation
id: rs777411418
seq_region_name: 17
source: dbSNP
start: 73385855
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385856
feature_type: variation
id: rs756230449
seq_region_name: 17
source: dbSNP
start: 73385856
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385857
feature_type: variation
id: rs1376459669
seq_region_name: 17
source: dbSNP
start: 73385857
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73385858
feature_type: variation
id: rs370015319
seq_region_name: 17
source: dbSNP
start: 73385858
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385861
feature_type: variation
id: rs2043474775
seq_region_name: 17
source: dbSNP
start: 73385861
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73385864
feature_type: variation
id: rs562611295
seq_region_name: 17
source: dbSNP
start: 73385864
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385865
feature_type: variation
id: rs757461777
seq_region_name: 17
source: dbSNP
start: 73385865
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385866
feature_type: variation
id: rs1178472142
seq_region_name: 17
source: dbSNP
start: 73385866
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385867
feature_type: variation
id: rs1306976502
seq_region_name: 17
source: dbSNP
start: 73385867
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385868
feature_type: variation
id: rs1369213454
seq_region_name: 17
source: dbSNP
start: 73385868
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385869
feature_type: variation
id: rs779227615
seq_region_name: 17
source: dbSNP
start: 73385869
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385876
feature_type: variation
id: rs533153750
seq_region_name: 17
source: dbSNP
start: 73385876
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385877
feature_type: variation
id: rs772568053
seq_region_name: 17
source: dbSNP
start: 73385877
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385878
feature_type: variation
id: rs201969715
seq_region_name: 17
source: dbSNP
start: 73385878
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385880
feature_type: variation
id: rs1368350429
seq_region_name: 17
source: dbSNP
start: 73385880
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385881
feature_type: variation
id: rs1466256538
seq_region_name: 17
source: dbSNP
start: 73385881
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385882
feature_type: variation
id: rs1172698655
seq_region_name: 17
source: dbSNP
start: 73385882
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73385883
feature_type: variation
id: rs117291342
seq_region_name: 17
source: dbSNP
start: 73385883
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385884
feature_type: variation
id: rs140102684
seq_region_name: 17
source: dbSNP
start: 73385884
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73385888
feature_type: variation
id: rs533638289
seq_region_name: 17
source: dbSNP
start: 73385888
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385889
feature_type: variation
id: rs377529553
seq_region_name: 17
source: dbSNP
start: 73385889
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385897
feature_type: variation
id: rs2062868076
seq_region_name: 17
source: dbSNP
start: 73385897
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385898
feature_type: variation
id: rs761500362
seq_region_name: 17
source: dbSNP
start: 73385898
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73385899
feature_type: variation
id: rs1188336607
seq_region_name: 17
source: dbSNP
start: 73385899
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385900
feature_type: variation
id: rs1599508621
seq_region_name: 17
source: dbSNP
start: 73385900
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385902
feature_type: variation
id: rs1303318978
seq_region_name: 17
source: dbSNP
start: 73385902
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385904
feature_type: variation
id: rs1283285215
seq_region_name: 17
source: dbSNP
start: 73385904
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385906
feature_type: variation
id: rs1317959718
seq_region_name: 17
source: dbSNP
start: 73385906
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73385910
feature_type: variation
id: rs78185984
seq_region_name: 17
source: dbSNP
start: 73385910
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385911
feature_type: variation
id: rs566939609
seq_region_name: 17
source: dbSNP
start: 73385911
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385912
feature_type: variation
id: rs762845048
seq_region_name: 17
source: dbSNP
start: 73385912
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73385913
feature_type: variation
id: rs1198336911
seq_region_name: 17
source: dbSNP
start: 73385913
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73385916
feature_type: variation
id: rs766358671
seq_region_name: 17
source: dbSNP
start: 73385916
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73385917
feature_type: variation
id: rs1444294007
seq_region_name: 17
source: dbSNP
start: 73385917
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73385920
feature_type: variation
id: rs751563081
seq_region_name: 17
source: dbSNP
start: 73385920
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73385921
feature_type: variation
id: rs1599508675
seq_region_name: 17
source: dbSNP
start: 73385921
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73385924
feature_type: variation
id: rs2145484290
seq_region_name: 17
source: dbSNP
start: 73385924
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73385927
feature_type: variation
id: rs1237164324
seq_region_name: 17
source: dbSNP
start: 73385927
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73385931
feature_type: variation
id: rs1478188486
seq_region_name: 17
source: dbSNP
start: 73385931
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385935
feature_type: variation
id: rs1172989221
seq_region_name: 17
source: dbSNP
start: 73385935
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385936
feature_type: variation
id: rs377614924
seq_region_name: 17
source: dbSNP
start: 73385936
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385937
feature_type: variation
id: rs1465065912
seq_region_name: 17
source: dbSNP
start: 73385937
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385938
feature_type: variation
id: rs537416500
seq_region_name: 17
source: dbSNP
start: 73385938
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385939
feature_type: variation
id: rs201358824
seq_region_name: 17
source: dbSNP
start: 73385939
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385940
feature_type: variation
id: rs2062868584
seq_region_name: 17
source: dbSNP
start: 73385940
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385941
feature_type: variation
id: rs2270719
seq_region_name: 17
source: dbSNP
start: 73385941
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385942
feature_type: variation
id: rs757491350
seq_region_name: 17
source: dbSNP
start: 73385942
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385943
feature_type: variation
id: rs1599508727
seq_region_name: 17
source: dbSNP
start: 73385943
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385948
feature_type: variation
id: rs1365774414
seq_region_name: 17
source: dbSNP
start: 73385948
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385951
feature_type: variation
id: rs779178238
seq_region_name: 17
source: dbSNP
start: 73385951
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385952
feature_type: variation
id: rs373973350
seq_region_name: 17
source: dbSNP
start: 73385952
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385953
feature_type: variation
id: rs377163312
seq_region_name: 17
source: dbSNP
start: 73385953
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385954
feature_type: variation
id: rs370285630
seq_region_name: 17
source: dbSNP
start: 73385954
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385962
feature_type: variation
id: rs570143868
seq_region_name: 17
source: dbSNP
start: 73385962
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385963
feature_type: variation
id: rs747517758
seq_region_name: 17
source: dbSNP
start: 73385963
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385964
feature_type: variation
id: rs1257148123
seq_region_name: 17
source: dbSNP
start: 73385964
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385966
feature_type: variation
id: rs77056196
seq_region_name: 17
source: dbSNP
start: 73385966
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385967
feature_type: variation
id: rs1199170145
seq_region_name: 17
source: dbSNP
start: 73385967
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385968
feature_type: variation
id: rs540712584
seq_region_name: 17
source: dbSNP
start: 73385968
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385969
feature_type: variation
id: rs2145484414
seq_region_name: 17
source: dbSNP
start: 73385969
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385971
feature_type: variation
id: rs1407231476
seq_region_name: 17
source: dbSNP
start: 73385971
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385973
feature_type: variation
id: rs1814540144
seq_region_name: 17
source: dbSNP
start: 73385973
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385976
feature_type: variation
id: rs1302065309
seq_region_name: 17
source: dbSNP
start: 73385976
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385979
feature_type: variation
id: rs959732942
seq_region_name: 17
source: dbSNP
start: 73385979
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385982
feature_type: variation
id: rs2062868969
seq_region_name: 17
source: dbSNP
start: 73385982
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385983
feature_type: variation
id: rs2145484435
seq_region_name: 17
source: dbSNP
start: 73385983
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385986
feature_type: variation
id: rs2062869005
seq_region_name: 17
source: dbSNP
start: 73385986
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385988
feature_type: variation
id: rs1188278029
seq_region_name: 17
source: dbSNP
start: 73385988
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385991
feature_type: variation
id: rs2062869038
seq_region_name: 17
source: dbSNP
start: 73385991
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385994
feature_type: variation
id: rs1332968585
seq_region_name: 17
source: dbSNP
start: 73385994
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385995
feature_type: variation
id: rs1450519606
seq_region_name: 17
source: dbSNP
start: 73385995
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73385996
feature_type: variation
id: rs1232201504
seq_region_name: 17
source: dbSNP
start: 73385996
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386002
feature_type: variation
id: rs2062869090
seq_region_name: 17
source: dbSNP
start: 73386002
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386008
feature_type: variation
id: rs1302902724
seq_region_name: 17
source: dbSNP
start: 73386008
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386010
feature_type: variation
id: rs555861086
seq_region_name: 17
source: dbSNP
start: 73386010
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73386120
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2062870171
seq_region_name: 17
source: dbSNP
start: 73386124
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1763697531
seq_region_name: 17
source: dbSNP
start: 73386126
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73386128
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs1599508954
seq_region_name: 17
source: dbSNP
start: 73386129
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386131
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73386138
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73386140
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73386141
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs905354557
seq_region_name: 17
source: dbSNP
start: 73386142
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062870310
seq_region_name: 17
source: dbSNP
start: 73386144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs559894310
seq_region_name: 17
source: dbSNP
start: 73386145
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs527449619
seq_region_name: 17
source: dbSNP
start: 73386146
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145484858
seq_region_name: 17
source: dbSNP
start: 73386153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062870390
seq_region_name: 17
source: dbSNP
start: 73386162
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386165
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062870428
seq_region_name: 17
source: dbSNP
start: 73386168
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062870449
seq_region_name: 17
source: dbSNP
start: 73386176
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1398909444
seq_region_name: 17
source: dbSNP
start: 73386177
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062870489
seq_region_name: 17
source: dbSNP
start: 73386183
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386196
feature_type: variation
id: rs866842451
seq_region_name: 17
source: dbSNP
start: 73386196
strand: 1
-
alleles:
- CCC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386200
feature_type: variation
id: rs1366164042
seq_region_name: 17
source: dbSNP
start: 73386198
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386199
feature_type: variation
id: rs2062870547
seq_region_name: 17
source: dbSNP
start: 73386199
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386200
feature_type: variation
id: rs185459826
seq_region_name: 17
source: dbSNP
start: 73386200
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062870593
seq_region_name: 17
source: dbSNP
start: 73386201
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386202
feature_type: variation
id: rs2062870612
seq_region_name: 17
source: dbSNP
start: 73386202
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386205
feature_type: variation
id: rs1019927157
seq_region_name: 17
source: dbSNP
start: 73386205
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386206
feature_type: variation
id: rs2062870659
seq_region_name: 17
source: dbSNP
start: 73386206
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386209
feature_type: variation
id: rs968379706
seq_region_name: 17
source: dbSNP
start: 73386209
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386210
feature_type: variation
id: rs1179258367
seq_region_name: 17
source: dbSNP
start: 73386210
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386219
feature_type: variation
id: rs978635828
seq_region_name: 17
source: dbSNP
start: 73386219
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386223
feature_type: variation
id: rs2062870730
seq_region_name: 17
source: dbSNP
start: 73386221
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386223
feature_type: variation
id: rs2062870763
seq_region_name: 17
source: dbSNP
start: 73386223
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386225
feature_type: variation
id: rs921877748
seq_region_name: 17
source: dbSNP
start: 73386225
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386226
feature_type: variation
id: rs1599509029
seq_region_name: 17
source: dbSNP
start: 73386226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386228
feature_type: variation
id: rs1180834396
seq_region_name: 17
source: dbSNP
start: 73386228
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386229
feature_type: variation
id: rs2062870859
seq_region_name: 17
source: dbSNP
start: 73386229
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386233
feature_type: variation
id: rs73999026
seq_region_name: 17
source: dbSNP
start: 73386233
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386234
feature_type: variation
id: rs531347185
seq_region_name: 17
source: dbSNP
start: 73386234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599509045
seq_region_name: 17
source: dbSNP
start: 73386236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062870963
seq_region_name: 17
source: dbSNP
start: 73386247
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs913691965
seq_region_name: 17
source: dbSNP
start: 73386247
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062871006
seq_region_name: 17
source: dbSNP
start: 73386251
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386253
feature_type: variation
id: rs2062871022
seq_region_name: 17
source: dbSNP
start: 73386253
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062871041
seq_region_name: 17
source: dbSNP
start: 73386256
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386257
feature_type: variation
id: rs549504238
seq_region_name: 17
source: dbSNP
start: 73386257
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1306643002
seq_region_name: 17
source: dbSNP
start: 73386259
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062871079
seq_region_name: 17
source: dbSNP
start: 73386261
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145485071
seq_region_name: 17
source: dbSNP
start: 73386262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs911944520
seq_region_name: 17
source: dbSNP
start: 73386263
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs190385725
seq_region_name: 17
source: dbSNP
start: 73386265
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062871139
seq_region_name: 17
source: dbSNP
start: 73386266
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386267
feature_type: variation
id: rs1205544382
seq_region_name: 17
source: dbSNP
start: 73386267
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1036338642
seq_region_name: 17
source: dbSNP
start: 73386270
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs979555092
seq_region_name: 17
source: dbSNP
start: 73386288
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062871211
seq_region_name: 17
source: dbSNP
start: 73386289
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386290
feature_type: variation
id: rs2062871230
seq_region_name: 17
source: dbSNP
start: 73386290
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386294
feature_type: variation
id: rs2062871253
seq_region_name: 17
source: dbSNP
start: 73386294
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386301
feature_type: variation
id: rs899145195
seq_region_name: 17
source: dbSNP
start: 73386301
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386302
feature_type: variation
id: rs1337704822
seq_region_name: 17
source: dbSNP
start: 73386302
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386303
feature_type: variation
id: rs1599509097
seq_region_name: 17
source: dbSNP
start: 73386303
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386305
feature_type: variation
id: rs1310885187
seq_region_name: 17
source: dbSNP
start: 73386305
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386306
feature_type: variation
id: rs2062871360
seq_region_name: 17
source: dbSNP
start: 73386306
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386313
feature_type: variation
id: rs930667105
seq_region_name: 17
source: dbSNP
start: 73386313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386314
feature_type: variation
id: rs924984827
seq_region_name: 17
source: dbSNP
start: 73386314
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386315
feature_type: variation
id: rs80092974
seq_region_name: 17
source: dbSNP
start: 73386315
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386322
feature_type: variation
id: rs2062871431
seq_region_name: 17
source: dbSNP
start: 73386322
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386323
feature_type: variation
id: rs1822057724
seq_region_name: 17
source: dbSNP
start: 73386323
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386326
feature_type: variation
id: rs905448618
seq_region_name: 17
source: dbSNP
start: 73386326
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386327
feature_type: variation
id: rs2062871483
seq_region_name: 17
source: dbSNP
start: 73386327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386328
feature_type: variation
id: rs1248154271
seq_region_name: 17
source: dbSNP
start: 73386328
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386330
feature_type: variation
id: rs2062871534
seq_region_name: 17
source: dbSNP
start: 73386330
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386331
feature_type: variation
id: rs2062871555
seq_region_name: 17
source: dbSNP
start: 73386331
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386332
feature_type: variation
id: rs1388567454
seq_region_name: 17
source: dbSNP
start: 73386332
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386334
feature_type: variation
id: rs1157713399
seq_region_name: 17
source: dbSNP
start: 73386334
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386336
feature_type: variation
id: rs374534412
seq_region_name: 17
source: dbSNP
start: 73386336
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386337
feature_type: variation
id: rs2062871643
seq_region_name: 17
source: dbSNP
start: 73386337
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386341
feature_type: variation
id: rs2270721
seq_region_name: 17
source: dbSNP
start: 73386341
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386342
feature_type: variation
id: rs2062871707
seq_region_name: 17
source: dbSNP
start: 73386342
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386343
feature_type: variation
id: rs944897565
seq_region_name: 17
source: dbSNP
start: 73386343
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386344
feature_type: variation
id: rs1423010735
seq_region_name: 17
source: dbSNP
start: 73386344
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386345
feature_type: variation
id: rs1260628406
seq_region_name: 17
source: dbSNP
start: 73386345
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386356
feature_type: variation
id: rs1185202746
seq_region_name: 17
source: dbSNP
start: 73386356
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386357
feature_type: variation
id: rs2062871768
seq_region_name: 17
source: dbSNP
start: 73386357
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386361
feature_type: variation
id: rs534364522
seq_region_name: 17
source: dbSNP
start: 73386361
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386364
feature_type: variation
id: rs2062871816
seq_region_name: 17
source: dbSNP
start: 73386364
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386366
feature_type: variation
id: rs1599509190
seq_region_name: 17
source: dbSNP
start: 73386366
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386366
feature_type: variation
id: rs1599509194
seq_region_name: 17
source: dbSNP
start: 73386366
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386367
feature_type: variation
id: rs2062871894
seq_region_name: 17
source: dbSNP
start: 73386367
strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386372
feature_type: variation
id: rs1568376184
seq_region_name: 17
source: dbSNP
start: 73386367
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386368
feature_type: variation
id: rs1599509203
seq_region_name: 17
source: dbSNP
start: 73386368
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386369
feature_type: variation
id: rs1428222791
seq_region_name: 17
source: dbSNP
start: 73386369
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs895544016
seq_region_name: 17
source: dbSNP
start: 73386370
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386371
feature_type: variation
id: rs1209392485
seq_region_name: 17
source: dbSNP
start: 73386371
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386372
feature_type: variation
id: rs897961766
seq_region_name: 17
source: dbSNP
start: 73386372
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386373
feature_type: variation
id: rs555902192
seq_region_name: 17
source: dbSNP
start: 73386373
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386374
feature_type: variation
id: rs2145485325
seq_region_name: 17
source: dbSNP
start: 73386374
strand: 1
-
alleles:
- AAAA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386381
feature_type: variation
id: rs2062872088
seq_region_name: 17
source: dbSNP
start: 73386378
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386382
feature_type: variation
id: rs2062872107
seq_region_name: 17
source: dbSNP
start: 73386382
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386387
feature_type: variation
id: rs1341302114
seq_region_name: 17
source: dbSNP
start: 73386387
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386388
feature_type: variation
id: rs2270722
seq_region_name: 17
source: dbSNP
start: 73386388
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386389
feature_type: variation
id: rs2062872148
seq_region_name: 17
source: dbSNP
start: 73386389
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386390
feature_type: variation
id: rs1599509259
seq_region_name: 17
source: dbSNP
start: 73386390
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386391
feature_type: variation
id: rs968346728
seq_region_name: 17
source: dbSNP
start: 73386391
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386394
feature_type: variation
id: rs1432990463
seq_region_name: 17
source: dbSNP
start: 73386394
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386395
feature_type: variation
id: rs2145485372
seq_region_name: 17
source: dbSNP
start: 73386395
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386398
feature_type: variation
id: rs1279869411
seq_region_name: 17
source: dbSNP
start: 73386398
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386400
feature_type: variation
id: rs1488740766
seq_region_name: 17
source: dbSNP
start: 73386400
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386404
feature_type: variation
id: rs376876675
seq_region_name: 17
source: dbSNP
start: 73386404
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386405
feature_type: variation
id: rs1261150101
seq_region_name: 17
source: dbSNP
start: 73386405
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386406
feature_type: variation
id: rs1386577102
seq_region_name: 17
source: dbSNP
start: 73386406
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386410
feature_type: variation
id: rs1161086629
seq_region_name: 17
source: dbSNP
start: 73386410
strand: 1
-
alleles:
- GAGAGAGAGA
- GAGAGA
- GAGAGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386422
feature_type: variation
id: rs1568376212
seq_region_name: 17
source: dbSNP
start: 73386413
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386415
feature_type: variation
id: rs1457033491
seq_region_name: 17
source: dbSNP
start: 73386415
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386417
feature_type: variation
id: rs544635980
seq_region_name: 17
source: dbSNP
start: 73386417
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386423
feature_type: variation
id: rs2062872486
seq_region_name: 17
source: dbSNP
start: 73386423
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386424
feature_type: variation
id: rs1599509303
seq_region_name: 17
source: dbSNP
start: 73386424
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386426
feature_type: variation
id: rs1199449207
seq_region_name: 17
source: dbSNP
start: 73386426
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386428
feature_type: variation
id: rs1379365764
seq_region_name: 17
source: dbSNP
start: 73386428
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386429
feature_type: variation
id: rs2062872573
seq_region_name: 17
source: dbSNP
start: 73386429
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386436
feature_type: variation
id: rs1476911334
seq_region_name: 17
source: dbSNP
start: 73386436
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73386437
feature_type: variation
id: rs1171795581
seq_region_name: 17
source: dbSNP
start: 73386437
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73386438
feature_type: variation
id: rs2062872639
seq_region_name: 17
source: dbSNP
start: 73386438
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73386440
feature_type: variation
id: rs2062872659
seq_region_name: 17
source: dbSNP
start: 73386440
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73386441
feature_type: variation
id: rs376993948
seq_region_name: 17
source: dbSNP
start: 73386441
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386445
feature_type: variation
id: rs1421173117
seq_region_name: 17
source: dbSNP
start: 73386445
strand: 1
-
alleles:
- GCCTGCAGG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73386455
feature_type: variation
id: rs2062872720
seq_region_name: 17
source: dbSNP
start: 73386447
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386448
feature_type: variation
id: rs1295761813
seq_region_name: 17
source: dbSNP
start: 73386448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386450
feature_type: variation
id: rs2062872769
seq_region_name: 17
source: dbSNP
start: 73386450
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386451
feature_type: variation
id: rs2062872796
seq_region_name: 17
source: dbSNP
start: 73386451
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386452
feature_type: variation
id: rs1359328594
seq_region_name: 17
source: dbSNP
start: 73386452
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386456
feature_type: variation
id: rs1386888830
seq_region_name: 17
source: dbSNP
start: 73386456
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386457
feature_type: variation
id: rs1599509366
seq_region_name: 17
source: dbSNP
start: 73386457
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386458
feature_type: variation
id: rs2062872910
seq_region_name: 17
source: dbSNP
start: 73386458
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386459
feature_type: variation
id: rs1302584410
seq_region_name: 17
source: dbSNP
start: 73386459
strand: 1
-
alleles:
- GTCAGT
- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73386464
feature_type: variation
id: rs1568376243
seq_region_name: 17
source: dbSNP
start: 73386459
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386460
feature_type: variation
id: rs2062872982
seq_region_name: 17
source: dbSNP
start: 73386460
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386463
feature_type: variation
id: rs1333395807
seq_region_name: 17
source: dbSNP
start: 73386463
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386464
feature_type: variation
id: rs1167464311
seq_region_name: 17
source: dbSNP
start: 73386464
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386467
feature_type: variation
id: rs1231455326
seq_region_name: 17
source: dbSNP
start: 73386467
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386469
feature_type: variation
id: rs1303165013
seq_region_name: 17
source: dbSNP
start: 73386469
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386470
feature_type: variation
id: rs769504258
seq_region_name: 17
source: dbSNP
start: 73386470
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386471
feature_type: variation
id: rs773011099
seq_region_name: 17
source: dbSNP
start: 73386471
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386473
feature_type: variation
id: rs1284190442
seq_region_name: 17
source: dbSNP
start: 73386473
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386475
feature_type: variation
id: rs1485581305
seq_region_name: 17
source: dbSNP
start: 73386475
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386476
feature_type: variation
id: rs749042053
seq_region_name: 17
source: dbSNP
start: 73386476
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386478
feature_type: variation
id: rs770882397
seq_region_name: 17
source: dbSNP
start: 73386478
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386479
feature_type: variation
id: rs370905236
seq_region_name: 17
source: dbSNP
start: 73386479
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386480
feature_type: variation
id: rs866159411
seq_region_name: 17
source: dbSNP
start: 73386480
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386481
feature_type: variation
id: rs774330092
seq_region_name: 17
source: dbSNP
start: 73386481
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73386483
feature_type: variation
id: rs374296270
seq_region_name: 17
source: dbSNP
start: 73386483
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386485
feature_type: variation
id: rs144767155
seq_region_name: 17
source: dbSNP
start: 73386485
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386487
feature_type: variation
id: rs776770822
seq_region_name: 17
source: dbSNP
start: 73386487
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386488
feature_type: variation
id: rs761807489
seq_region_name: 17
source: dbSNP
start: 73386488
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386490
feature_type: variation
id: rs1265275730
seq_region_name: 17
source: dbSNP
start: 73386490
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386491
feature_type: variation
id: rs868780506
seq_region_name: 17
source: dbSNP
start: 73386491
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386492
feature_type: variation
id: rs2062873468
seq_region_name: 17
source: dbSNP
start: 73386492
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386493
feature_type: variation
id: rs1457959939
seq_region_name: 17
source: dbSNP
start: 73386493
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386496
feature_type: variation
id: rs1294791549
seq_region_name: 17
source: dbSNP
start: 73386496
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386497
feature_type: variation
id: rs1393433900
seq_region_name: 17
source: dbSNP
start: 73386497
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386498
feature_type: variation
id: rs1385610216
seq_region_name: 17
source: dbSNP
start: 73386498
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386499
feature_type: variation
id: rs765387304
seq_region_name: 17
source: dbSNP
start: 73386499
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386503
feature_type: variation
id: rs2145485741
seq_region_name: 17
source: dbSNP
start: 73386503
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73386504
feature_type: variation
id: rs750669601
seq_region_name: 17
source: dbSNP
start: 73386504
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386507
feature_type: variation
id: rs1013415637
seq_region_name: 17
source: dbSNP
start: 73386507
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386509
feature_type: variation
id: rs148565589
seq_region_name: 17
source: dbSNP
start: 73386509
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386510
feature_type: variation
id: rs766705397
seq_region_name: 17
source: dbSNP
start: 73386510
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386512
feature_type: variation
id: rs868513030
seq_region_name: 17
source: dbSNP
start: 73386512
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386515
feature_type: variation
id: rs953426371
seq_region_name: 17
source: dbSNP
start: 73386515
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73386517
feature_type: variation
id: rs556280806
seq_region_name: 17
source: dbSNP
start: 73386517
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386518
feature_type: variation
id: rs1320945257
seq_region_name: 17
source: dbSNP
start: 73386518
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386519
feature_type: variation
id: rs368464336
seq_region_name: 17
source: dbSNP
start: 73386519
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73386520
feature_type: variation
id: rs866006487
seq_region_name: 17
source: dbSNP
start: 73386520
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386521
feature_type: variation
id: rs1487436688
seq_region_name: 17
source: dbSNP
start: 73386521
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386525
feature_type: variation
id: rs911731504
seq_region_name: 17
source: dbSNP
start: 73386525
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386526
feature_type: variation
id: rs2062873928
seq_region_name: 17
source: dbSNP
start: 73386526
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386527
feature_type: variation
id: rs1212968634
seq_region_name: 17
source: dbSNP
start: 73386527
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73386533
feature_type: variation
id: rs371894396
seq_region_name: 17
source: dbSNP
start: 73386533
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73386534
feature_type: variation
id: rs1458924964
seq_region_name: 17
source: dbSNP
start: 73386534
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386535
feature_type: variation
id: rs143657622
seq_region_name: 17
source: dbSNP
start: 73386535
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386538
feature_type: variation
id: rs1249317457
seq_region_name: 17
source: dbSNP
start: 73386538
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73386539
feature_type: variation
id: rs1424037277
seq_region_name: 17
source: dbSNP
start: 73386539
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386540
feature_type: variation
id: rs2062874137
seq_region_name: 17
source: dbSNP
start: 73386540
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386541
feature_type: variation
id: rs142963601
seq_region_name: 17
source: dbSNP
start: 73386541
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73386547
feature_type: variation
id: rs1297021550
seq_region_name: 17
source: dbSNP
start: 73386547
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73386548
feature_type: variation
id: rs770757861
seq_region_name: 17
source: dbSNP
start: 73386548
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73386549
feature_type: variation
id: rs2062874237
seq_region_name: 17
source: dbSNP
start: 73386549
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73386551
feature_type: variation
id: rs1457003743
seq_region_name: 17
source: dbSNP
start: 73386551
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73386552
feature_type: variation
id: rs138265085
seq_region_name: 17
source: dbSNP
start: 73386552
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73386556
feature_type: variation
id: rs1401733585
seq_region_name: 17
source: dbSNP
start: 73386556
strand: 1
-
alleles:
- AGAAATCAGGGCCAA
- AGAAATCAGGGCCAAGAAATCAGGGCCAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386571
feature_type: variation
id: rs2062874315
seq_region_name: 17
source: dbSNP
start: 73386557
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73386561
feature_type: variation
id: rs745720684
seq_region_name: 17
source: dbSNP
start: 73386561
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73386563
feature_type: variation
id: rs771983427
seq_region_name: 17
source: dbSNP
start: 73386563
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73386564
feature_type: variation
id: rs1340297881
seq_region_name: 17
source: dbSNP
start: 73386564
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73386565
feature_type: variation
id: rs775305232
seq_region_name: 17
source: dbSNP
start: 73386565
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386566
feature_type: variation
id: rs1271295066
seq_region_name: 17
source: dbSNP
start: 73386566
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386571
feature_type: variation
id: rs930592127
seq_region_name: 17
source: dbSNP
start: 73386571
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386572
feature_type: variation
id: rs2062874480
seq_region_name: 17
source: dbSNP
start: 73386572
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386573
feature_type: variation
id: rs1315165890
seq_region_name: 17
source: dbSNP
start: 73386573
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386575
feature_type: variation
id: rs2062874526
seq_region_name: 17
source: dbSNP
start: 73386575
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386580
feature_type: variation
id: rs1319972722
seq_region_name: 17
source: dbSNP
start: 73386580
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386581
feature_type: variation
id: rs1232822565
seq_region_name: 17
source: dbSNP
start: 73386581
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386583
feature_type: variation
id: rs1216483183
seq_region_name: 17
source: dbSNP
start: 73386583
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386584
feature_type: variation
id: rs2062874592
seq_region_name: 17
source: dbSNP
start: 73386584
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386591
feature_type: variation
id: rs1273991997
seq_region_name: 17
source: dbSNP
start: 73386591
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386593
feature_type: variation
id: rs1258622336
seq_region_name: 17
source: dbSNP
start: 73386593
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386594
feature_type: variation
id: rs2062874670
seq_region_name: 17
source: dbSNP
start: 73386594
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386596
feature_type: variation
id: rs1319933368
seq_region_name: 17
source: dbSNP
start: 73386596
strand: 1
-
alleles:
- C
- T
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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alleles:
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386710
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386727
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386737
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386739
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386742
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73386748
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73386752
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73386759
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386760
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73386761
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73386767
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73386769
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73386770
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386771
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73386778
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386786
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386791
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386793
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386794
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386797
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386799
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1020804958
seq_region_name: 17
source: dbSNP
start: 73386802
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs571138319
seq_region_name: 17
source: dbSNP
start: 73386804
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386806
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386807
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386811
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386812
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73386812
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386819
feature_type: variation
id: rs75880465
seq_region_name: 17
source: dbSNP
start: 73386819
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386821
feature_type: variation
id: rs183582862
seq_region_name: 17
source: dbSNP
start: 73386821
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386823
feature_type: variation
id: rs1032125285
seq_region_name: 17
source: dbSNP
start: 73386823
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73386824
feature_type: variation
id: rs980775520
seq_region_name: 17
source: dbSNP
start: 73386824
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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source: dbSNP
start: 73387047
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73387048
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387051
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73387072
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062878608
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1406921657
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062878663
seq_region_name: 17
source: dbSNP
start: 73387077
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062878698
seq_region_name: 17
source: dbSNP
start: 73387078
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1033804779
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599510202
seq_region_name: 17
source: dbSNP
start: 73387086
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145486910
seq_region_name: 17
source: dbSNP
start: 73387088
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs560895174
seq_region_name: 17
source: dbSNP
start: 73387089
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1297910877
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387096
strand: 1
-
alleles:
- ATTACAGGCAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062878827
seq_region_name: 17
source: dbSNP
start: 73387097
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs960986972
seq_region_name: 17
source: dbSNP
start: 73387107
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1356759377
seq_region_name: 17
source: dbSNP
start: 73387107
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs576119157
seq_region_name: 17
source: dbSNP
start: 73387110
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062878918
seq_region_name: 17
source: dbSNP
start: 73387111
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599510239
seq_region_name: 17
source: dbSNP
start: 73387114
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062878984
seq_region_name: 17
source: dbSNP
start: 73387117
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145486954
seq_region_name: 17
source: dbSNP
start: 73387121
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1430938799
seq_region_name: 17
source: dbSNP
start: 73387122
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs992172793
seq_region_name: 17
source: dbSNP
start: 73387123
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387124
feature_type: variation
id: rs1032599426
seq_region_name: 17
source: dbSNP
start: 73387124
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062879069
seq_region_name: 17
source: dbSNP
start: 73387126
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145486974
seq_region_name: 17
source: dbSNP
start: 73387132
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1481181172
seq_region_name: 17
source: dbSNP
start: 73387134
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249191953
seq_region_name: 17
source: dbSNP
start: 73387135
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387140
feature_type: variation
id: rs1271126941
seq_region_name: 17
source: dbSNP
start: 73387140
strand: 1
-
alleles:
- AGAGA
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1480863942
seq_region_name: 17
source: dbSNP
start: 73387143
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062879163
seq_region_name: 17
source: dbSNP
start: 73387144
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062879181
seq_region_name: 17
source: dbSNP
start: 73387148
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387149
feature_type: variation
id: rs2062879195
seq_region_name: 17
source: dbSNP
start: 73387149
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387150
feature_type: variation
id: rs889599289
seq_region_name: 17
source: dbSNP
start: 73387150
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387152
feature_type: variation
id: rs145073850
seq_region_name: 17
source: dbSNP
start: 73387152
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387156
feature_type: variation
id: rs564967323
seq_region_name: 17
source: dbSNP
start: 73387156
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387158
feature_type: variation
id: rs2062879290
seq_region_name: 17
source: dbSNP
start: 73387158
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387161
feature_type: variation
id: rs945642760
seq_region_name: 17
source: dbSNP
start: 73387161
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387162
feature_type: variation
id: rs1213185015
seq_region_name: 17
source: dbSNP
start: 73387162
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387168
feature_type: variation
id: rs778127913
seq_region_name: 17
source: dbSNP
start: 73387168
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387170
feature_type: variation
id: rs1225448932
seq_region_name: 17
source: dbSNP
start: 73387170
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387172
feature_type: variation
id: rs2062879383
seq_region_name: 17
source: dbSNP
start: 73387172
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387174
feature_type: variation
id: rs2062879407
seq_region_name: 17
source: dbSNP
start: 73387174
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387185
feature_type: variation
id: rs2062879432
seq_region_name: 17
source: dbSNP
start: 73387185
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387186
feature_type: variation
id: rs2062879458
seq_region_name: 17
source: dbSNP
start: 73387186
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387188
feature_type: variation
id: rs1348820737
seq_region_name: 17
source: dbSNP
start: 73387188
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387193
feature_type: variation
id: rs925435951
seq_region_name: 17
source: dbSNP
start: 73387193
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387195
feature_type: variation
id: rs932863999
seq_region_name: 17
source: dbSNP
start: 73387195
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387201
feature_type: variation
id: rs2062879557
seq_region_name: 17
source: dbSNP
start: 73387201
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387202
feature_type: variation
id: rs2062879585
seq_region_name: 17
source: dbSNP
start: 73387202
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387204
feature_type: variation
id: rs747562925
seq_region_name: 17
source: dbSNP
start: 73387204
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387205
feature_type: variation
id: rs567648377
seq_region_name: 17
source: dbSNP
start: 73387205
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387206
feature_type: variation
id: rs536703738
seq_region_name: 17
source: dbSNP
start: 73387206
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387207
feature_type: variation
id: rs944338822
seq_region_name: 17
source: dbSNP
start: 73387207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387208
feature_type: variation
id: rs1251289375
seq_region_name: 17
source: dbSNP
start: 73387208
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387211
feature_type: variation
id: rs767249759
seq_region_name: 17
source: dbSNP
start: 73387211
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387212
feature_type: variation
id: rs1026608300
seq_region_name: 17
source: dbSNP
start: 73387212
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387213
feature_type: variation
id: rs2062879761
seq_region_name: 17
source: dbSNP
start: 73387213
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387219
feature_type: variation
id: rs2062879778
seq_region_name: 17
source: dbSNP
start: 73387219
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387221
feature_type: variation
id: rs2062879800
seq_region_name: 17
source: dbSNP
start: 73387221
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387223
feature_type: variation
id: rs2062879829
seq_region_name: 17
source: dbSNP
start: 73387223
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387232
feature_type: variation
id: rs897721701
seq_region_name: 17
source: dbSNP
start: 73387232
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387235
feature_type: variation
id: rs560808693
seq_region_name: 17
source: dbSNP
start: 73387235
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387236
feature_type: variation
id: rs527988761
seq_region_name: 17
source: dbSNP
start: 73387236
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387237
feature_type: variation
id: rs2062879950
seq_region_name: 17
source: dbSNP
start: 73387237
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387239
feature_type: variation
id: rs746034590
seq_region_name: 17
source: dbSNP
start: 73387239
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387240
feature_type: variation
id: rs549627422
seq_region_name: 17
source: dbSNP
start: 73387240
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387242
feature_type: variation
id: rs1243704218
seq_region_name: 17
source: dbSNP
start: 73387242
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387247
feature_type: variation
id: rs2145487207
seq_region_name: 17
source: dbSNP
start: 73387247
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387248
feature_type: variation
id: rs2145487210
seq_region_name: 17
source: dbSNP
start: 73387249
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387249
feature_type: variation
id: rs1002080905
seq_region_name: 17
source: dbSNP
start: 73387249
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387250
feature_type: variation
id: rs1034139028
seq_region_name: 17
source: dbSNP
start: 73387250
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387252
feature_type: variation
id: rs960828160
seq_region_name: 17
source: dbSNP
start: 73387252
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387254
feature_type: variation
id: rs992538141
seq_region_name: 17
source: dbSNP
start: 73387254
strand: 1
-
alleles:
- "-"
- CAAAGTTCTGGGATTATAGGCGTCAGCCACGCGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387254
feature_type: variation
id: rs2145487231
seq_region_name: 17
source: dbSNP
start: 73387255
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387255
feature_type: variation
id: rs1318964333
seq_region_name: 17
source: dbSNP
start: 73387255
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387257
feature_type: variation
id: rs902479034
seq_region_name: 17
source: dbSNP
start: 73387257
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387258
feature_type: variation
id: rs2062880240
seq_region_name: 17
source: dbSNP
start: 73387258
strand: 1
-
alleles:
- CTCTCT
- CTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387264
feature_type: variation
id: rs1452400850
seq_region_name: 17
source: dbSNP
start: 73387259
strand: 1
-
alleles:
- TCTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387265
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73387405
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387419
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73387420
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387426
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73387436
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73387438
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73387442
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387445
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387446
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387450
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387451
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs990939652
seq_region_name: 17
source: dbSNP
start: 73387452
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387455
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387457
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387458
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062882140
seq_region_name: 17
source: dbSNP
start: 73387461
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387463
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387467
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387468
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387470
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387473
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387476
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387478
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145487675
seq_region_name: 17
source: dbSNP
start: 73387481
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387482
feature_type: variation
id: rs150866934
seq_region_name: 17
source: dbSNP
start: 73387482
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387483
feature_type: variation
id: rs1280971725
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73387590
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73387601
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73387603
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387603
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73387614
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73387622
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73387624
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387629
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387633
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73387634
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387640
strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs1280289850
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs75985368
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1349516852
seq_region_name: 17
source: dbSNP
start: 73387645
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387646
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062883789
seq_region_name: 17
source: dbSNP
start: 73387648
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1279868333
seq_region_name: 17
source: dbSNP
start: 73387652
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062883852
seq_region_name: 17
source: dbSNP
start: 73387659
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145488020
seq_region_name: 17
source: dbSNP
start: 73387660
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062883873
seq_region_name: 17
source: dbSNP
start: 73387661
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387663
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062883927
seq_region_name: 17
source: dbSNP
start: 73387666
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387668
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387668
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387672
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387672
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387673
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs896307527
seq_region_name: 17
source: dbSNP
start: 73387674
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387677
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387675
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387676
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73387676
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145488077
seq_region_name: 17
source: dbSNP
start: 73387677
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387679
feature_type: variation
id: rs2062884077
seq_region_name: 17
source: dbSNP
start: 73387679
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387681
feature_type: variation
id: rs1316324696
seq_region_name: 17
source: dbSNP
start: 73387681
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs751970269
seq_region_name: 17
source: dbSNP
start: 73387683
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062884149
seq_region_name: 17
source: dbSNP
start: 73387686
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387688
feature_type: variation
id: rs1409019745
seq_region_name: 17
source: dbSNP
start: 73387688
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387689
feature_type: variation
id: rs547419941
seq_region_name: 17
source: dbSNP
start: 73387689
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387690
feature_type: variation
id: rs902615047
seq_region_name: 17
source: dbSNP
start: 73387690
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387691
feature_type: variation
id: rs1184813820
seq_region_name: 17
source: dbSNP
start: 73387691
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387695
feature_type: variation
id: rs888195029
seq_region_name: 17
source: dbSNP
start: 73387691
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387693
feature_type: variation
id: rs1055466551
seq_region_name: 17
source: dbSNP
start: 73387693
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387695
feature_type: variation
id: rs1000794386
seq_region_name: 17
source: dbSNP
start: 73387695
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387697
feature_type: variation
id: rs73999027
seq_region_name: 17
source: dbSNP
start: 73387697
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387698
feature_type: variation
id: rs1025164583
seq_region_name: 17
source: dbSNP
start: 73387698
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387700
feature_type: variation
id: rs2062884510
seq_region_name: 17
source: dbSNP
start: 73387700
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387701
feature_type: variation
id: rs2062884535
seq_region_name: 17
source: dbSNP
start: 73387701
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387702
feature_type: variation
id: rs2145488142
seq_region_name: 17
source: dbSNP
start: 73387702
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387703
feature_type: variation
id: rs1242019987
seq_region_name: 17
source: dbSNP
start: 73387703
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387704
feature_type: variation
id: rs2062884570
seq_region_name: 17
source: dbSNP
start: 73387704
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387706
feature_type: variation
id: rs954210787
seq_region_name: 17
source: dbSNP
start: 73387706
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387707
feature_type: variation
id: rs2062884614
seq_region_name: 17
source: dbSNP
start: 73387707
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387708
feature_type: variation
id: rs1599510847
seq_region_name: 17
source: dbSNP
start: 73387708
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387711
feature_type: variation
id: rs2062884663
seq_region_name: 17
source: dbSNP
start: 73387711
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387712
feature_type: variation
id: rs2062884692
seq_region_name: 17
source: dbSNP
start: 73387712
strand: 1
-
alleles:
- AGGAGGAG
- AGGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387722
feature_type: variation
id: rs2062884717
seq_region_name: 17
source: dbSNP
start: 73387715
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387717
feature_type: variation
id: rs970899031
seq_region_name: 17
source: dbSNP
start: 73387717
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387722
feature_type: variation
id: rs1330965510
seq_region_name: 17
source: dbSNP
start: 73387722
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387726
feature_type: variation
id: rs2062884805
seq_region_name: 17
source: dbSNP
start: 73387726
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387730
feature_type: variation
id: rs999692469
seq_region_name: 17
source: dbSNP
start: 73387730
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387741
feature_type: variation
id: rs2062884859
seq_region_name: 17
source: dbSNP
start: 73387741
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387743
feature_type: variation
id: rs1599510866
seq_region_name: 17
source: dbSNP
start: 73387743
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387744
feature_type: variation
id: rs1031544857
seq_region_name: 17
source: dbSNP
start: 73387744
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387746
feature_type: variation
id: rs1381270682
seq_region_name: 17
source: dbSNP
start: 73387746
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387756
feature_type: variation
id: rs1007131912
seq_region_name: 17
source: dbSNP
start: 73387756
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387760
feature_type: variation
id: rs1287144727
seq_region_name: 17
source: dbSNP
start: 73387756
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387757
feature_type: variation
id: rs1334000755
seq_region_name: 17
source: dbSNP
start: 73387757
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387758
feature_type: variation
id: rs2062885017
seq_region_name: 17
source: dbSNP
start: 73387758
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387767
feature_type: variation
id: rs2062885042
seq_region_name: 17
source: dbSNP
start: 73387767
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387769
feature_type: variation
id: rs1320588769
seq_region_name: 17
source: dbSNP
start: 73387769
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387770
feature_type: variation
id: rs1423117634
seq_region_name: 17
source: dbSNP
start: 73387770
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387772
feature_type: variation
id: rs1365267944
seq_region_name: 17
source: dbSNP
start: 73387772
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387773
feature_type: variation
id: rs2062885140
seq_region_name: 17
source: dbSNP
start: 73387773
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387777
feature_type: variation
id: rs1599510895
seq_region_name: 17
source: dbSNP
start: 73387777
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387779
feature_type: variation
id: rs1238432512
seq_region_name: 17
source: dbSNP
start: 73387779
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387780
feature_type: variation
id: rs1020321888
seq_region_name: 17
source: dbSNP
start: 73387780
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387783
feature_type: variation
id: rs2062885231
seq_region_name: 17
source: dbSNP
start: 73387783
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387786
feature_type: variation
id: rs1418029009
seq_region_name: 17
source: dbSNP
start: 73387786
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387787
feature_type: variation
id: rs1250584281
seq_region_name: 17
source: dbSNP
start: 73387787
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387788
feature_type: variation
id: rs1483481361
seq_region_name: 17
source: dbSNP
start: 73387788
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387789
feature_type: variation
id: rs765266551
seq_region_name: 17
source: dbSNP
start: 73387789
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387790
feature_type: variation
id: rs2062885351
seq_region_name: 17
source: dbSNP
start: 73387790
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387791
feature_type: variation
id: rs989939816
seq_region_name: 17
source: dbSNP
start: 73387791
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387792
feature_type: variation
id: rs374081798
seq_region_name: 17
source: dbSNP
start: 73387792
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387793
feature_type: variation
id: rs1568376864
seq_region_name: 17
source: dbSNP
start: 73387793
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387794
feature_type: variation
id: rs1193767594
seq_region_name: 17
source: dbSNP
start: 73387794
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387795
feature_type: variation
id: rs1424882036
seq_region_name: 17
source: dbSNP
start: 73387795
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387796
feature_type: variation
id: rs1599510940
seq_region_name: 17
source: dbSNP
start: 73387796
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387799
feature_type: variation
id: rs200043982
seq_region_name: 17
source: dbSNP
start: 73387799
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387800
feature_type: variation
id: rs1469348082
seq_region_name: 17
source: dbSNP
start: 73387800
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387801
feature_type: variation
id: rs2062885534
seq_region_name: 17
source: dbSNP
start: 73387801
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387802
feature_type: variation
id: rs1168718074
seq_region_name: 17
source: dbSNP
start: 73387802
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387803
feature_type: variation
id: rs1354290106
seq_region_name: 17
source: dbSNP
start: 73387803
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387804
feature_type: variation
id: rs2145488351
seq_region_name: 17
source: dbSNP
start: 73387804
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387805
feature_type: variation
id: rs2062885615
seq_region_name: 17
source: dbSNP
start: 73387805
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387810
feature_type: variation
id: rs774058400
seq_region_name: 17
source: dbSNP
start: 73387807
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387817
feature_type: variation
id: rs2062885653
seq_region_name: 17
source: dbSNP
start: 73387817
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387819
feature_type: variation
id: rs558928799
seq_region_name: 17
source: dbSNP
start: 73387819
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387820
feature_type: variation
id: rs1377322415
seq_region_name: 17
source: dbSNP
start: 73387820
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387822
feature_type: variation
id: rs1414188062
seq_region_name: 17
source: dbSNP
start: 73387822
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387823
feature_type: variation
id: rs1599510986
seq_region_name: 17
source: dbSNP
start: 73387823
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387824
feature_type: variation
id: rs755310400
seq_region_name: 17
source: dbSNP
start: 73387824
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387826
feature_type: variation
id: rs201624486
seq_region_name: 17
source: dbSNP
start: 73387826
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73387827
feature_type: variation
id: rs1216693513
seq_region_name: 17
source: dbSNP
start: 73387827
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73387829
feature_type: variation
id: rs1272249264
seq_region_name: 17
source: dbSNP
start: 73387829
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73387830
feature_type: variation
id: rs140330374
seq_region_name: 17
source: dbSNP
start: 73387830
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73387831
feature_type: variation
id: rs1212041438
seq_region_name: 17
source: dbSNP
start: 73387831
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73387834
feature_type: variation
id: rs2062885925
seq_region_name: 17
source: dbSNP
start: 73387834
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387837
feature_type: variation
id: rs2062885948
seq_region_name: 17
source: dbSNP
start: 73387837
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73387840
feature_type: variation
id: rs748864651
seq_region_name: 17
source: dbSNP
start: 73387840
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387842
feature_type: variation
id: rs375758688
seq_region_name: 17
source: dbSNP
start: 73387842
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387845
feature_type: variation
id: rs1216650267
seq_region_name: 17
source: dbSNP
start: 73387845
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73387846
feature_type: variation
id: rs778438588
seq_region_name: 17
source: dbSNP
start: 73387846
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387851
feature_type: variation
id: rs1476582992
seq_region_name: 17
source: dbSNP
start: 73387851
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387854
feature_type: variation
id: rs745623040
seq_region_name: 17
source: dbSNP
start: 73387854
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387858
feature_type: variation
id: rs1345137997
seq_region_name: 17
source: dbSNP
start: 73387858
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73387859
feature_type: variation
id: rs115502230
seq_region_name: 17
source: dbSNP
start: 73387859
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387860
feature_type: variation
id: rs200974788
seq_region_name: 17
source: dbSNP
start: 73387860
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387861
feature_type: variation
id: rs1403348660
seq_region_name: 17
source: dbSNP
start: 73387861
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387864
feature_type: variation
id: rs1178708604
seq_region_name: 17
source: dbSNP
start: 73387864
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73387870
feature_type: variation
id: rs369928391
seq_region_name: 17
source: dbSNP
start: 73387870
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387871
feature_type: variation
id: rs35928335
seq_region_name: 17
source: dbSNP
start: 73387871
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387877
feature_type: variation
id: rs2270723
seq_region_name: 17
source: dbSNP
start: 73387877
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387878
feature_type: variation
id: rs1362499999
seq_region_name: 17
source: dbSNP
start: 73387878
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387882
feature_type: variation
id: rs1398297332
seq_region_name: 17
source: dbSNP
start: 73387882
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387883
feature_type: variation
id: rs2062886480
seq_region_name: 17
source: dbSNP
start: 73387883
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387884
feature_type: variation
id: rs370137730
seq_region_name: 17
source: dbSNP
start: 73387884
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387886
feature_type: variation
id: rs774459256
seq_region_name: 17
source: dbSNP
start: 73387886
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387887
feature_type: variation
id: rs759903925
seq_region_name: 17
source: dbSNP
start: 73387887
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73387890
feature_type: variation
id: rs2062886626
seq_region_name: 17
source: dbSNP
start: 73387890
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387891
feature_type: variation
id: rs202115079
seq_region_name: 17
source: dbSNP
start: 73387891
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387892
feature_type: variation
id: rs1318467320
seq_region_name: 17
source: dbSNP
start: 73387892
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387894
feature_type: variation
id: rs753163364
seq_region_name: 17
source: dbSNP
start: 73387894
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387897
feature_type: variation
id: rs147771806
seq_region_name: 17
source: dbSNP
start: 73387897
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387898
feature_type: variation
id: rs144178058
seq_region_name: 17
source: dbSNP
start: 73387898
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387899
feature_type: variation
id: rs1240393836
seq_region_name: 17
source: dbSNP
start: 73387899
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387903
feature_type: variation
id: rs753332803
seq_region_name: 17
source: dbSNP
start: 73387903
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387905
feature_type: variation
id: rs1487020674
seq_region_name: 17
source: dbSNP
start: 73387905
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387909
feature_type: variation
id: rs756845155
seq_region_name: 17
source: dbSNP
start: 73387909
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387910
feature_type: variation
id: rs372583655
seq_region_name: 17
source: dbSNP
start: 73387910
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387911
feature_type: variation
id: rs377237314
seq_region_name: 17
source: dbSNP
start: 73387911
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387912
feature_type: variation
id: rs1193249182
seq_region_name: 17
source: dbSNP
start: 73387912
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387914
feature_type: variation
id: rs1275508497
seq_region_name: 17
source: dbSNP
start: 73387914
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73387918
feature_type: variation
id: rs2145488682
seq_region_name: 17
source: dbSNP
start: 73387918
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387921
feature_type: variation
id: rs758115187
seq_region_name: 17
source: dbSNP
start: 73387921
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387922
feature_type: variation
id: rs1221796918
seq_region_name: 17
source: dbSNP
start: 73387922
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387924
feature_type: variation
id: rs1599511202
seq_region_name: 17
source: dbSNP
start: 73387924
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387925
feature_type: variation
id: rs779697322
seq_region_name: 17
source: dbSNP
start: 73387925
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387928
feature_type: variation
id: rs2062887222
seq_region_name: 17
source: dbSNP
start: 73387928
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387929
feature_type: variation
id: rs1336097235
seq_region_name: 17
source: dbSNP
start: 73387929
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387932
feature_type: variation
id: rs1159465982
seq_region_name: 17
source: dbSNP
start: 73387932
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387933
feature_type: variation
id: rs746868582
seq_region_name: 17
source: dbSNP
start: 73387933
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387934
feature_type: variation
id: rs1398963118
seq_region_name: 17
source: dbSNP
start: 73387934
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: missense_variant
end: 73387941
feature_type: variation
id: rs2270724
seq_region_name: 17
source: dbSNP
start: 73387941
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387942
feature_type: variation
id: rs2062887346
seq_region_name: 17
source: dbSNP
start: 73387942
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387943
feature_type: variation
id: rs781120547
seq_region_name: 17
source: dbSNP
start: 73387943
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387944
feature_type: variation
id: rs1438550022
seq_region_name: 17
source: dbSNP
start: 73387944
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387945
feature_type: variation
id: rs1323864491
seq_region_name: 17
source: dbSNP
start: 73387945
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387946
feature_type: variation
id: rs1369934430
seq_region_name: 17
source: dbSNP
start: 73387946
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387948
feature_type: variation
id: rs749315984
seq_region_name: 17
source: dbSNP
start: 73387948
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387949
feature_type: variation
id: rs1310984655
seq_region_name: 17
source: dbSNP
start: 73387949
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387951
feature_type: variation
id: rs144987400
seq_region_name: 17
source: dbSNP
start: 73387951
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387952
feature_type: variation
id: rs369725380
seq_region_name: 17
source: dbSNP
start: 73387952
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387953
feature_type: variation
id: rs1236501889
seq_region_name: 17
source: dbSNP
start: 73387953
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387954
feature_type: variation
id: rs1568377035
seq_region_name: 17
source: dbSNP
start: 73387954
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73387957
feature_type: variation
id: rs1568377038
seq_region_name: 17
source: dbSNP
start: 73387955
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73387958
feature_type: variation
id: rs200242323
seq_region_name: 17
source: dbSNP
start: 73387958
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387959
feature_type: variation
id: rs775994536
seq_region_name: 17
source: dbSNP
start: 73387959
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387960
feature_type: variation
id: rs1224404728
seq_region_name: 17
source: dbSNP
start: 73387960
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387961
feature_type: variation
id: rs1251747976
seq_region_name: 17
source: dbSNP
start: 73387961
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73387964
feature_type: variation
id: rs538868108
seq_region_name: 17
source: dbSNP
start: 73387964
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387967
feature_type: variation
id: rs2062887817
seq_region_name: 17
source: dbSNP
start: 73387967
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387968
feature_type: variation
id: rs1179665134
seq_region_name: 17
source: dbSNP
start: 73387968
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387976
feature_type: variation
id: rs1240184376
seq_region_name: 17
source: dbSNP
start: 73387976
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387977
feature_type: variation
id: rs2062887914
seq_region_name: 17
source: dbSNP
start: 73387977
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73387978
feature_type: variation
id: rs149093785
seq_region_name: 17
source: dbSNP
start: 73387978
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387979
feature_type: variation
id: rs764640694
seq_region_name: 17
source: dbSNP
start: 73387979
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73387979
feature_type: variation
id: rs1568377072
seq_region_name: 17
source: dbSNP
start: 73387979
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73387981
feature_type: variation
id: rs780369029
seq_region_name: 17
source: dbSNP
start: 73387981
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387983
feature_type: variation
id: rs565119878
seq_region_name: 17
source: dbSNP
start: 73387983
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73387984
feature_type: variation
id: rs558804353
seq_region_name: 17
source: dbSNP
start: 73387984
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387987
feature_type: variation
id: rs1162699017
seq_region_name: 17
source: dbSNP
start: 73387987
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387990
feature_type: variation
id: rs1201828506
seq_region_name: 17
source: dbSNP
start: 73387990
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387991
feature_type: variation
id: rs1393719098
seq_region_name: 17
source: dbSNP
start: 73387991
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73387993
feature_type: variation
id: rs1025833156
seq_region_name: 17
source: dbSNP
start: 73387993
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73387997
feature_type: variation
id: rs1447176338
seq_region_name: 17
source: dbSNP
start: 73387997
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73387999
feature_type: variation
id: rs866769820
seq_region_name: 17
source: dbSNP
start: 73387999
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73388000
feature_type: variation
id: rs1333126538
seq_region_name: 17
source: dbSNP
start: 73388000
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388002
feature_type: variation
id: rs867554923
seq_region_name: 17
source: dbSNP
start: 73388002
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388003
feature_type: variation
id: rs2062888347
seq_region_name: 17
source: dbSNP
start: 73388003
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73388006
feature_type: variation
id: rs1333585052
seq_region_name: 17
source: dbSNP
start: 73388006
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388009
feature_type: variation
id: rs952879149
seq_region_name: 17
source: dbSNP
start: 73388009
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73388010
feature_type: variation
id: rs951279575
seq_region_name: 17
source: dbSNP
start: 73388010
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388011
feature_type: variation
id: rs866244479
seq_region_name: 17
source: dbSNP
start: 73388011
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73388012
feature_type: variation
id: rs147384840
seq_region_name: 17
source: dbSNP
start: 73388012
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388013
feature_type: variation
id: rs909729322
seq_region_name: 17
source: dbSNP
start: 73388013
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73388015
feature_type: variation
id: rs779759743
seq_region_name: 17
source: dbSNP
start: 73388015
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388017
feature_type: variation
id: rs751293920
seq_region_name: 17
source: dbSNP
start: 73388017
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388018
feature_type: variation
id: rs866613394
seq_region_name: 17
source: dbSNP
start: 73388018
strand: 1
-
alleles:
- CTGGGGGGCTGCGGAC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73388034
feature_type: variation
id: rs2062888691
seq_region_name: 17
source: dbSNP
start: 73388019
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73388021
feature_type: variation
id: rs754789240
seq_region_name: 17
source: dbSNP
start: 73388021
strand: 1
-
alleles:
- GGGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73388026
feature_type: variation
id: rs759253697
seq_region_name: 17
source: dbSNP
start: 73388021
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388022
feature_type: variation
id: rs2062888785
seq_region_name: 17
source: dbSNP
start: 73388022
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73388024
feature_type: variation
id: rs1260419984
seq_region_name: 17
source: dbSNP
start: 73388024
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388025
feature_type: variation
id: rs2145489198
seq_region_name: 17
source: dbSNP
start: 73388025
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388026
feature_type: variation
id: rs781065583
seq_region_name: 17
source: dbSNP
start: 73388026
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73388027
feature_type: variation
id: rs2062888880
seq_region_name: 17
source: dbSNP
start: 73388027
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388028
feature_type: variation
id: rs2062888909
seq_region_name: 17
source: dbSNP
start: 73388028
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73388030
feature_type: variation
id: rs139527427
seq_region_name: 17
source: dbSNP
start: 73388030
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388034
feature_type: variation
id: rs778845493
seq_region_name: 17
source: dbSNP
start: 73388034
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388035
feature_type: variation
id: rs368436418
seq_region_name: 17
source: dbSNP
start: 73388035
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73388036
feature_type: variation
id: rs1185917110
seq_region_name: 17
source: dbSNP
start: 73388036
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73388037
feature_type: variation
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388074
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062889845
seq_region_name: 17
source: dbSNP
start: 73388080
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1053090015
seq_region_name: 17
source: dbSNP
start: 73388081
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388082
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062889937
seq_region_name: 17
source: dbSNP
start: 73388083
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73388085
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388087
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062890058
seq_region_name: 17
source: dbSNP
start: 73388092
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs776618013
seq_region_name: 17
source: dbSNP
start: 73388100
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388106
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs534782866
seq_region_name: 17
source: dbSNP
start: 73388107
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388109
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388110
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388119
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73388125
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388129
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388131
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388134
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388138
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1260898609
seq_region_name: 17
source: dbSNP
start: 73388144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388145
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388147
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1189674350
seq_region_name: 17
source: dbSNP
start: 73388152
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388152
feature_type: variation
id: rs2062890413
seq_region_name: 17
source: dbSNP
start: 73388152
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388155
feature_type: variation
id: rs1486670816
seq_region_name: 17
source: dbSNP
start: 73388155
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388158
feature_type: variation
id: rs2062890463
seq_region_name: 17
source: dbSNP
start: 73388158
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062890489
seq_region_name: 17
source: dbSNP
start: 73388159
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388167
feature_type: variation
id: rs2062890511
seq_region_name: 17
source: dbSNP
start: 73388167
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062890534
seq_region_name: 17
source: dbSNP
start: 73388170
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388171
feature_type: variation
id: rs901400453
seq_region_name: 17
source: dbSNP
start: 73388171
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388172
feature_type: variation
id: rs375461723
seq_region_name: 17
source: dbSNP
start: 73388172
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388174
feature_type: variation
id: rs1029675865
seq_region_name: 17
source: dbSNP
start: 73388174
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062890629
seq_region_name: 17
source: dbSNP
start: 73388175
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1477774982
seq_region_name: 17
source: dbSNP
start: 73388181
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388183
feature_type: variation
id: rs2062890675
seq_region_name: 17
source: dbSNP
start: 73388183
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388184
feature_type: variation
id: rs574574996
seq_region_name: 17
source: dbSNP
start: 73388184
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388190
feature_type: variation
id: rs1189182612
seq_region_name: 17
source: dbSNP
start: 73388190
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs951429073
seq_region_name: 17
source: dbSNP
start: 73388194
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388195
feature_type: variation
id: rs765027573
seq_region_name: 17
source: dbSNP
start: 73388195
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388196
feature_type: variation
id: rs1474236710
seq_region_name: 17
source: dbSNP
start: 73388196
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388199
feature_type: variation
id: rs775054334
seq_region_name: 17
source: dbSNP
start: 73388199
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388200
feature_type: variation
id: rs1246335219
seq_region_name: 17
source: dbSNP
start: 73388200
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388201
feature_type: variation
id: rs1324237999
seq_region_name: 17
source: dbSNP
start: 73388201
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388203
feature_type: variation
id: rs2062890891
seq_region_name: 17
source: dbSNP
start: 73388203
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388204
feature_type: variation
id: rs2062890913
seq_region_name: 17
source: dbSNP
start: 73388204
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388205
feature_type: variation
id: rs2062890933
seq_region_name: 17
source: dbSNP
start: 73388205
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388207
feature_type: variation
id: rs2062890967
seq_region_name: 17
source: dbSNP
start: 73388207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388208
feature_type: variation
id: rs1294233072
seq_region_name: 17
source: dbSNP
start: 73388208
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388209
feature_type: variation
id: rs2145489762
seq_region_name: 17
source: dbSNP
start: 73388209
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388210
feature_type: variation
id: rs1400166550
seq_region_name: 17
source: dbSNP
start: 73388210
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388213
feature_type: variation
id: rs2062891028
seq_region_name: 17
source: dbSNP
start: 73388213
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388222
feature_type: variation
id: rs1288297734
seq_region_name: 17
source: dbSNP
start: 73388222
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388227
feature_type: variation
id: rs1301022815
seq_region_name: 17
source: dbSNP
start: 73388227
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388232
feature_type: variation
id: rs2062891096
seq_region_name: 17
source: dbSNP
start: 73388232
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388236
feature_type: variation
id: rs2062891122
seq_region_name: 17
source: dbSNP
start: 73388236
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388237
feature_type: variation
id: rs80289990
seq_region_name: 17
source: dbSNP
start: 73388237
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388241
feature_type: variation
id: rs1484332468
seq_region_name: 17
source: dbSNP
start: 73388241
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388243
feature_type: variation
id: rs1391341416
seq_region_name: 17
source: dbSNP
start: 73388243
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388247
feature_type: variation
id: rs1568377279
seq_region_name: 17
source: dbSNP
start: 73388247
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388248
feature_type: variation
id: rs2062891207
seq_region_name: 17
source: dbSNP
start: 73388248
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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-
alleles:
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-
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alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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-
alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388347
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73388349
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73388356
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73388360
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388364
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73388365
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388366
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388367
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388373
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388375
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73388376
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388377
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388379
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388385
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs911283744
seq_region_name: 17
source: dbSNP
start: 73388387
strand: 1
-
alleles:
- TGAGCAGGATGAG
- TGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388388
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388389
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388394
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388400
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388400
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388401
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145490146
seq_region_name: 17
source: dbSNP
start: 73388402
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388403
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062892505
seq_region_name: 17
source: dbSNP
start: 73388405
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1051157436
seq_region_name: 17
source: dbSNP
start: 73388406
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062892548
seq_region_name: 17
source: dbSNP
start: 73388407
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062892568
seq_region_name: 17
source: dbSNP
start: 73388411
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388412
feature_type: variation
id: rs1568377370
seq_region_name: 17
source: dbSNP
start: 73388412
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388413
feature_type: variation
id: rs1379951732
seq_region_name: 17
source: dbSNP
start: 73388413
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388414
feature_type: variation
id: rs367794336
seq_region_name: 17
source: dbSNP
start: 73388414
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062892650
seq_region_name: 17
source: dbSNP
start: 73388416
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388419
feature_type: variation
id: rs1336173325
seq_region_name: 17
source: dbSNP
start: 73388419
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388420
feature_type: variation
id: rs552522706
seq_region_name: 17
source: dbSNP
start: 73388420
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388421
feature_type: variation
id: rs1427561449
seq_region_name: 17
source: dbSNP
start: 73388421
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388427
feature_type: variation
id: rs2062892730
seq_region_name: 17
source: dbSNP
start: 73388427
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388430
feature_type: variation
id: rs1157157864
seq_region_name: 17
source: dbSNP
start: 73388430
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388433
feature_type: variation
id: rs2062892778
seq_region_name: 17
source: dbSNP
start: 73388433
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388434
feature_type: variation
id: rs751022027
seq_region_name: 17
source: dbSNP
start: 73388434
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388436
feature_type: variation
id: rs1004613881
seq_region_name: 17
source: dbSNP
start: 73388436
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388437
feature_type: variation
id: rs2062892836
seq_region_name: 17
source: dbSNP
start: 73388437
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388440
feature_type: variation
id: rs1181136503
seq_region_name: 17
source: dbSNP
start: 73388440
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388444
feature_type: variation
id: rs922582930
seq_region_name: 17
source: dbSNP
start: 73388444
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388445
feature_type: variation
id: rs2062892896
seq_region_name: 17
source: dbSNP
start: 73388445
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388447
feature_type: variation
id: rs929994831
seq_region_name: 17
source: dbSNP
start: 73388447
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388448
feature_type: variation
id: rs2145490286
seq_region_name: 17
source: dbSNP
start: 73388448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388449
feature_type: variation
id: rs2062892956
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs375693838
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs146751981
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1209957387
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599511893
seq_region_name: 17
source: dbSNP
start: 73388545
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388548
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388549
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062894002
seq_region_name: 17
source: dbSNP
start: 73388550
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062894040
seq_region_name: 17
source: dbSNP
start: 73388554
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1472872934
seq_region_name: 17
source: dbSNP
start: 73388560
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062894107
seq_region_name: 17
source: dbSNP
start: 73388563
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs117683710
seq_region_name: 17
source: dbSNP
start: 73388574
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73388575
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1190491840
seq_region_name: 17
source: dbSNP
start: 73388577
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062894203
seq_region_name: 17
source: dbSNP
start: 73388577
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1481636831
seq_region_name: 17
source: dbSNP
start: 73388583
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599511932
seq_region_name: 17
source: dbSNP
start: 73388588
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs539014505
seq_region_name: 17
source: dbSNP
start: 73388591
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs894667597
seq_region_name: 17
source: dbSNP
start: 73388595
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145490611
seq_region_name: 17
source: dbSNP
start: 73388597
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062894309
seq_region_name: 17
source: dbSNP
start: 73388600
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs914203661
seq_region_name: 17
source: dbSNP
start: 73388602
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1012396232
seq_region_name: 17
source: dbSNP
start: 73388604
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062894369
seq_region_name: 17
source: dbSNP
start: 73388606
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388609
feature_type: variation
id: rs1599511950
seq_region_name: 17
source: dbSNP
start: 73388609
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388610
feature_type: variation
id: rs1357148845
seq_region_name: 17
source: dbSNP
start: 73388610
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388611
feature_type: variation
id: rs36145410
seq_region_name: 17
source: dbSNP
start: 73388611
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73388612
feature_type: variation
id: rs1228952826
seq_region_name: 17
source: dbSNP
start: 73388612
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388613
feature_type: variation
id: rs921449996
seq_region_name: 17
source: dbSNP
start: 73388613
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388614
feature_type: variation
id: rs2062894536
seq_region_name: 17
source: dbSNP
start: 73388614
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388616
feature_type: variation
id: rs577114711
seq_region_name: 17
source: dbSNP
start: 73388616
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388624
feature_type: variation
id: rs1399575473
seq_region_name: 17
source: dbSNP
start: 73388624
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388626
feature_type: variation
id: rs999152547
seq_region_name: 17
source: dbSNP
start: 73388626
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388632
feature_type: variation
id: rs2062894626
seq_region_name: 17
source: dbSNP
start: 73388632
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388633
feature_type: variation
id: rs1413715811
seq_region_name: 17
source: dbSNP
start: 73388633
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388638
feature_type: variation
id: rs2062894676
seq_region_name: 17
source: dbSNP
start: 73388638
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388639
feature_type: variation
id: rs1300395657
seq_region_name: 17
source: dbSNP
start: 73388639
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388644
feature_type: variation
id: rs2145490692
seq_region_name: 17
source: dbSNP
start: 73388644
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388651
feature_type: variation
id: rs2062894710
seq_region_name: 17
source: dbSNP
start: 73388651
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388656
feature_type: variation
id: rs1423177208
seq_region_name: 17
source: dbSNP
start: 73388656
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388657
feature_type: variation
id: rs1030843339
seq_region_name: 17
source: dbSNP
start: 73388657
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388659
feature_type: variation
id: rs1599511986
seq_region_name: 17
source: dbSNP
start: 73388659
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388660
feature_type: variation
id: rs2062894792
seq_region_name: 17
source: dbSNP
start: 73388660
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388672
feature_type: variation
id: rs958209802
seq_region_name: 17
source: dbSNP
start: 73388672
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388677
feature_type: variation
id: rs1407579119
seq_region_name: 17
source: dbSNP
start: 73388677
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388680
feature_type: variation
id: rs2062894863
seq_region_name: 17
source: dbSNP
start: 73388680
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388686
feature_type: variation
id: rs541275770
seq_region_name: 17
source: dbSNP
start: 73388686
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388692
feature_type: variation
id: rs1165670186
seq_region_name: 17
source: dbSNP
start: 73388692
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388695
feature_type: variation
id: rs2062894932
seq_region_name: 17
source: dbSNP
start: 73388695
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388699
feature_type: variation
id: rs141238638
seq_region_name: 17
source: dbSNP
start: 73388699
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388702
feature_type: variation
id: rs2062894989
seq_region_name: 17
source: dbSNP
start: 73388702
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388707
feature_type: variation
id: rs2062895015
seq_region_name: 17
source: dbSNP
start: 73388707
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388708
feature_type: variation
id: rs1477266100
seq_region_name: 17
source: dbSNP
start: 73388707
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388710
feature_type: variation
id: rs754068958
seq_region_name: 17
source: dbSNP
start: 73388710
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388713
feature_type: variation
id: rs2062895084
seq_region_name: 17
source: dbSNP
start: 73388713
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388715
feature_type: variation
id: rs2062895108
seq_region_name: 17
source: dbSNP
start: 73388715
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388716
feature_type: variation
id: rs1330139669
seq_region_name: 17
source: dbSNP
start: 73388716
strand: 1
-
alleles:
- TTCTTCTTC
- TTCTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388727
feature_type: variation
id: rs2062895152
seq_region_name: 17
source: dbSNP
start: 73388719
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388722
feature_type: variation
id: rs559500616
seq_region_name: 17
source: dbSNP
start: 73388722
strand: 1
-
alleles:
- CTTCCTTCCCTCCCTTCCTTCCCTCCCT
- CTTCCTTCCCTCCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388751
feature_type: variation
id: rs1038787532
seq_region_name: 17
source: dbSNP
start: 73388724
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388725
feature_type: variation
id: rs2062895237
seq_region_name: 17
source: dbSNP
start: 73388725
strand: 1
-
alleles:
- TCCCTCCCTTCCTTCCCTCCCTCC
- TCCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388753
feature_type: variation
id: rs1489815914
seq_region_name: 17
source: dbSNP
start: 73388730
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388733
feature_type: variation
id: rs2062895277
seq_region_name: 17
source: dbSNP
start: 73388731
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388733
feature_type: variation
id: rs2062895298
seq_region_name: 17
source: dbSNP
start: 73388733
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388735
feature_type: variation
id: rs1599512020
seq_region_name: 17
source: dbSNP
start: 73388735
strand: 1
-
alleles:
- CCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTC
- CCTTCCTTCCCTCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs2062895350
seq_region_name: 17
source: dbSNP
start: 73388736
strand: 1
-
alleles:
- CCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- CCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- CCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs759939801
seq_region_name: 17
source: dbSNP
start: 73388736
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388738
feature_type: variation
id: rs2062895444
seq_region_name: 17
source: dbSNP
start: 73388738
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388739
feature_type: variation
id: rs2062895479
seq_region_name: 17
source: dbSNP
start: 73388738
strand: 1
-
alleles:
- CTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388776
feature_type: variation
id: rs2062895499
seq_region_name: 17
source: dbSNP
start: 73388741
strand: 1
-
alleles:
- TCCCTCCCTCC
- TCCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388753
feature_type: variation
id: rs2062895528
seq_region_name: 17
source: dbSNP
start: 73388743
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388746
feature_type: variation
id: rs1246052411
seq_region_name: 17
source: dbSNP
start: 73388746
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388747
feature_type: variation
id: rs1599512032
seq_region_name: 17
source: dbSNP
start: 73388747
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388749
feature_type: variation
id: rs2062895632
seq_region_name: 17
source: dbSNP
start: 73388749
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388750
feature_type: variation
id: rs867556979
seq_region_name: 17
source: dbSNP
start: 73388750
strand: 1
-
alleles:
- CTC
- CTCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388752
feature_type: variation
id: rs1222130694
seq_region_name: 17
source: dbSNP
start: 73388750
strand: 1
-
alleles:
- CTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
- CTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388787
feature_type: variation
id: rs2062895743
seq_region_name: 17
source: dbSNP
start: 73388750
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388751
feature_type: variation
id: rs1599512045
seq_region_name: 17
source: dbSNP
start: 73388751
strand: 1
-
alleles:
- TCCTTCCTTCCTTCC
- TCCTTCC
- TCCTTCCTTCC
- TCCTTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388765
feature_type: variation
id: rs1270914728
seq_region_name: 17
source: dbSNP
start: 73388751
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388791
feature_type: variation
id: rs2062895820
seq_region_name: 17
source: dbSNP
start: 73388751
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTC
- TCCTTCCTTCCTTCCCTCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388798
feature_type: variation
id: rs2062895845
seq_region_name: 17
source: dbSNP
start: 73388751
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCC
- TCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388811
feature_type: variation
id: rs2062895876
seq_region_name: 17
source: dbSNP
start: 73388751
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- TCCTTCCTTCCTTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs2062895897
seq_region_name: 17
source: dbSNP
start: 73388751
strand: 1
-
alleles:
- CC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388753
feature_type: variation
id: rs2062895915
seq_region_name: 17
source: dbSNP
start: 73388752
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388754
feature_type: variation
id: rs1218131362
seq_region_name: 17
source: dbSNP
start: 73388753
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388754
feature_type: variation
id: rs1318836056
seq_region_name: 17
source: dbSNP
start: 73388754
strand: 1
-
alleles:
- TT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388755
feature_type: variation
id: rs2062896001
seq_region_name: 17
source: dbSNP
start: 73388754
strand: 1
-
alleles:
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388798
feature_type: variation
id: rs2062896020
seq_region_name: 17
source: dbSNP
start: 73388755
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388756
feature_type: variation
id: rs2062896042
seq_region_name: 17
source: dbSNP
start: 73388756
strand: 1
-
alleles:
- CTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388800
feature_type: variation
id: rs2062896063
seq_region_name: 17
source: dbSNP
start: 73388757
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388758
feature_type: variation
id: rs2145491000
seq_region_name: 17
source: dbSNP
start: 73388758
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388759
feature_type: variation
id: rs2062896078
seq_region_name: 17
source: dbSNP
start: 73388759
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388760
feature_type: variation
id: rs1280390530
seq_region_name: 17
source: dbSNP
start: 73388760
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388761
feature_type: variation
id: rs1300822985
seq_region_name: 17
source: dbSNP
start: 73388760
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388761
feature_type: variation
id: rs1403483527
seq_region_name: 17
source: dbSNP
start: 73388761
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388762
feature_type: variation
id: rs1599512067
seq_region_name: 17
source: dbSNP
start: 73388762
strand: 1
-
alleles:
- TCCCTCCCTC
- TCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388772
feature_type: variation
id: rs1367258872
seq_region_name: 17
source: dbSNP
start: 73388763
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388764
feature_type: variation
id: rs1294499997
seq_region_name: 17
source: dbSNP
start: 73388764
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388765
feature_type: variation
id: rs1439157594
seq_region_name: 17
source: dbSNP
start: 73388765
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388766
feature_type: variation
id: rs1219040321
seq_region_name: 17
source: dbSNP
start: 73388766
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388767
feature_type: variation
id: rs1599512098
seq_region_name: 17
source: dbSNP
start: 73388767
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388769
feature_type: variation
id: rs1167662712
seq_region_name: 17
source: dbSNP
start: 73388769
strand: 1
-
alleles:
- CCTCTCCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388776
feature_type: variation
id: rs2062896288
seq_region_name: 17
source: dbSNP
start: 73388769
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388770
feature_type: variation
id: rs1274266758
seq_region_name: 17
source: dbSNP
start: 73388770
strand: 1
-
alleles:
- CTCTC
- C
- CTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388774
feature_type: variation
id: rs1464691834
seq_region_name: 17
source: dbSNP
start: 73388770
strand: 1
-
alleles:
- CTCTCCTTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388778
feature_type: variation
id: rs2062896374
seq_region_name: 17
source: dbSNP
start: 73388770
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388771
feature_type: variation
id: rs1599512112
seq_region_name: 17
source: dbSNP
start: 73388771
strand: 1
-
alleles:
- TCTCCTTC
- TC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388778
feature_type: variation
id: rs1934265288
seq_region_name: 17
source: dbSNP
start: 73388771
strand: 1
-
alleles:
- TCTCCTTCCTTC
- TC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388782
feature_type: variation
id: rs1423876633
seq_region_name: 17
source: dbSNP
start: 73388771
strand: 1
-
alleles:
- CTCCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388776
feature_type: variation
id: rs2062896458
seq_region_name: 17
source: dbSNP
start: 73388772
strand: 1
-
alleles:
- "-"
- CT
- CTTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388772
feature_type: variation
id: rs2062896475
seq_region_name: 17
source: dbSNP
start: 73388773
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388773
feature_type: variation
id: rs199803323
seq_region_name: 17
source: dbSNP
start: 73388773
strand: 1
-
alleles:
- TCCTTCC
- TCCTTCCCTCCCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388779
feature_type: variation
id: rs746153716
seq_region_name: 17
source: dbSNP
start: 73388773
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCTTCC
- TCCTTCC
- TCCTTCCTTCC
- TCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388791
feature_type: variation
id: rs376691038
seq_region_name: 17
source: dbSNP
start: 73388773
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCC
- TCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388837
feature_type: variation
id: rs2062896592
seq_region_name: 17
source: dbSNP
start: 73388773
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388775
feature_type: variation
id: rs201323553
seq_region_name: 17
source: dbSNP
start: 73388775
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388775
feature_type: variation
id: rs2145491169
seq_region_name: 17
source: dbSNP
start: 73388776
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388776
feature_type: variation
id: rs202074169
seq_region_name: 17
source: dbSNP
start: 73388776
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388777
feature_type: variation
id: rs866213270
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCC
- TCCCTCCCTCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388779
feature_type: variation
id: rs2062896673
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCC
- TCCTTCCCTCCCTCTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388783
feature_type: variation
id: rs2062896693
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCC
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388787
feature_type: variation
id: rs2062896715
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCT
- TCCTTCCTTCCTTCCCTACCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388793
feature_type: variation
id: rs2062896741
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTC
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388798
feature_type: variation
id: rs2062896761
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCC
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388807
feature_type: variation
id: rs2062896791
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCT
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTATCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388817
feature_type: variation
id: rs2062896824
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTC
- TCCTTCCTTCCTTCCCTCCCTC
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs1191580854
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs1555757102
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCCCCTCCTTTCCTTTTCTTTCTCCCTCTCTTTTCTCCCTCCTTCTCTTCCTTCTCCCTCCCTCCCTCCCTCCCTCCCTTTTTCCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388922
feature_type: variation
id: rs2062896905
seq_region_name: 17
source: dbSNP
start: 73388777
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388779
feature_type: variation
id: rs2062896932
seq_region_name: 17
source: dbSNP
start: 73388778
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388780
feature_type: variation
id: rs2062896944
seq_region_name: 17
source: dbSNP
start: 73388780
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388781
feature_type: variation
id: rs867340546
seq_region_name: 17
source: dbSNP
start: 73388781
strand: 1
-
alleles:
- TCCTTCC
- TCCTTCCCTCCCTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388787
feature_type: variation
id: rs2062897029
seq_region_name: 17
source: dbSNP
start: 73388781
strand: 1
-
alleles:
- TCCTTCCTTCCCTCCCTCCTTCCTTCC
- TCCTTCCTTCC
- TCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388807
feature_type: variation
id: rs1489402286
seq_region_name: 17
source: dbSNP
start: 73388781
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388783
feature_type: variation
id: rs2062897089
seq_region_name: 17
source: dbSNP
start: 73388782
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388783
feature_type: variation
id: rs2062897115
seq_region_name: 17
source: dbSNP
start: 73388783
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388784
feature_type: variation
id: rs2062897135
seq_region_name: 17
source: dbSNP
start: 73388784
strand: 1
-
alleles:
- TT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388785
feature_type: variation
id: rs2145491294
seq_region_name: 17
source: dbSNP
start: 73388784
strand: 1
-
alleles:
- TCCTTCCCTCC
- TCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388795
feature_type: variation
id: rs1198067554
seq_region_name: 17
source: dbSNP
start: 73388785
strand: 1
-
alleles:
- TCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCC
- TCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCGTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388825
feature_type: variation
id: rs2145491300
seq_region_name: 17
source: dbSNP
start: 73388785
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388786
feature_type: variation
id: rs574871796
seq_region_name: 17
source: dbSNP
start: 73388786
strand: 1
-
alleles:
- CC
- C
- CCCTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388787
feature_type: variation
id: rs1469068399
seq_region_name: 17
source: dbSNP
start: 73388786
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388788
feature_type: variation
id: rs2145491320
seq_region_name: 17
source: dbSNP
start: 73388787
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388788
feature_type: variation
id: rs1260077101
seq_region_name: 17
source: dbSNP
start: 73388788
strand: 1
-
alleles:
- TCCCTCCCTCC
- TCCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388799
feature_type: variation
id: rs1251381624
seq_region_name: 17
source: dbSNP
start: 73388789
strand: 1
-
alleles:
- CCTCCCTCCT
- CCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388800
feature_type: variation
id: rs1311846421
seq_region_name: 17
source: dbSNP
start: 73388791
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388792
feature_type: variation
id: rs1257900286
seq_region_name: 17
source: dbSNP
start: 73388792
strand: 1
-
alleles:
- CTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCCCCTCCTTTCCTTTTCTTTCTCCCTCTCTTTTCTCCCTCCTTC
- CTCCCTCCTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388881
feature_type: variation
id: rs2062897307
seq_region_name: 17
source: dbSNP
start: 73388792
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388793
feature_type: variation
id: rs1221333112
seq_region_name: 17
source: dbSNP
start: 73388793
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388793
feature_type: variation
id: rs1331326600
seq_region_name: 17
source: dbSNP
start: 73388793
strand: 1
-
alleles:
- TCCCTCCTTCC
- TCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388803
feature_type: variation
id: rs1371781500
seq_region_name: 17
source: dbSNP
start: 73388793
strand: 1
-
alleles:
- TCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- TCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs1568377528
seq_region_name: 17
source: dbSNP
start: 73388793
strand: 1
-
alleles:
- CCC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388796
feature_type: variation
id: rs1941848671
seq_region_name: 17
source: dbSNP
start: 73388794
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388795
feature_type: variation
id: rs2062897400
seq_region_name: 17
source: dbSNP
start: 73388795
strand: 1
-
alleles:
- CCTCCT
- CCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388800
feature_type: variation
id: rs1445401295
seq_region_name: 17
source: dbSNP
start: 73388795
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388796
feature_type: variation
id: rs1400309462
seq_region_name: 17
source: dbSNP
start: 73388796
strand: 1
-
alleles:
- CTC
- CTCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388798
feature_type: variation
id: rs2055025051
seq_region_name: 17
source: dbSNP
start: 73388796
strand: 1
-
alleles:
- CTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCCCCTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388843
feature_type: variation
id: rs2062897475
seq_region_name: 17
source: dbSNP
start: 73388796
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388797
feature_type: variation
id: rs1568377535
seq_region_name: 17
source: dbSNP
start: 73388797
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388797
feature_type: variation
id: rs1599512221
seq_region_name: 17
source: dbSNP
start: 73388797
strand: 1
-
alleles:
- TC
- TCTCCTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388798
feature_type: variation
id: rs1332809496
seq_region_name: 17
source: dbSNP
start: 73388797
strand: 1
-
alleles:
- TCCTTCCTTCC
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388807
feature_type: variation
id: rs2062897567
seq_region_name: 17
source: dbSNP
start: 73388797
strand: 1
-
alleles:
- TCCTTCCTTCCTTCC
- TCCTTCC
- TCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388811
feature_type: variation
id: rs200670674
seq_region_name: 17
source: dbSNP
start: 73388797
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- TCCTTCCTTCCTTCCC
- TCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs1358255241
seq_region_name: 17
source: dbSNP
start: 73388797
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388798
feature_type: variation
id: rs1176487779
seq_region_name: 17
source: dbSNP
start: 73388798
strand: 1
-
alleles:
- CCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
- CCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs1186936281
seq_region_name: 17
source: dbSNP
start: 73388798
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388799
feature_type: variation
id: rs2062897674
seq_region_name: 17
source: dbSNP
start: 73388799
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388800
feature_type: variation
id: rs1421528711
seq_region_name: 17
source: dbSNP
start: 73388799
strand: 1
-
alleles:
- CTTCCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388804
feature_type: variation
id: rs1434742740
seq_region_name: 17
source: dbSNP
start: 73388799
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388800
feature_type: variation
id: rs200307811
seq_region_name: 17
source: dbSNP
start: 73388800
strand: 1
-
alleles:
- TT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388801
feature_type: variation
id: rs2062897771
seq_region_name: 17
source: dbSNP
start: 73388800
strand: 1
-
alleles:
- TCCTTCC
- TCCTTCCCTCCCTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388807
feature_type: variation
id: rs1177855856
seq_region_name: 17
source: dbSNP
start: 73388801
strand: 1
-
alleles:
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCC
- TCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388829
feature_type: variation
id: rs202206500
seq_region_name: 17
source: dbSNP
start: 73388801
strand: 1
-
alleles:
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs1568377548
seq_region_name: 17
source: dbSNP
start: 73388801
strand: 1
-
alleles:
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
- TCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs2062897867
seq_region_name: 17
source: dbSNP
start: 73388801
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388802
feature_type: variation
id: rs1408200499
seq_region_name: 17
source: dbSNP
start: 73388802
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388803
feature_type: variation
id: rs2062897929
seq_region_name: 17
source: dbSNP
start: 73388803
strand: 1
-
alleles:
- CTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCCCCCTCCTTTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388848
feature_type: variation
id: rs2062897952
seq_region_name: 17
source: dbSNP
start: 73388803
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388804
feature_type: variation
id: rs2062897973
seq_region_name: 17
source: dbSNP
start: 73388804
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388805
feature_type: variation
id: rs1394501481
seq_region_name: 17
source: dbSNP
start: 73388805
strand: 1
-
alleles:
- TCCTTCCCTCCCTCTCCTTCC
- TCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388825
feature_type: variation
id: rs1169325146
seq_region_name: 17
source: dbSNP
start: 73388805
strand: 1
-
alleles:
- TCCTTCCCTCCCTCTCCTTCCTTCCTTCC
- TCCTTCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTCCTTCCGTCCTTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2145491532
seq_region_name: 17
source: dbSNP
start: 73388805
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388807
feature_type: variation
id: rs1201882054
seq_region_name: 17
source: dbSNP
start: 73388807
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388808
feature_type: variation
id: rs201140498
seq_region_name: 17
source: dbSNP
start: 73388808
strand: 1
-
alleles:
- TT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388809
feature_type: variation
id: rs1568377564
seq_region_name: 17
source: dbSNP
start: 73388808
strand: 1
-
alleles:
- TCCCTCCCTC
- TCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs1256861480
seq_region_name: 17
source: dbSNP
start: 73388809
strand: 1
-
alleles:
- TCCCTCCCTCTCC
- TCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388821
feature_type: variation
id: rs2062898128
seq_region_name: 17
source: dbSNP
start: 73388809
strand: 1
-
alleles:
- TCCCTCCCTCTCCTTCCTTCCTTCC
- TCCCTCCCTCTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCGTCCCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2145491567
seq_region_name: 17
source: dbSNP
start: 73388809
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388810
feature_type: variation
id: rs2062898150
seq_region_name: 17
source: dbSNP
start: 73388810
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388810
feature_type: variation
id: rs2062898168
seq_region_name: 17
source: dbSNP
start: 73388811
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388811
feature_type: variation
id: rs1212667990
seq_region_name: 17
source: dbSNP
start: 73388811
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388812
feature_type: variation
id: rs1323428457
seq_region_name: 17
source: dbSNP
start: 73388812
strand: 1
-
alleles:
- CTCCCTCTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388820
feature_type: variation
id: rs2062898243
seq_region_name: 17
source: dbSNP
start: 73388812
strand: 1
-
alleles:
- CTCCCTCTCCTTCCTTCCTTCC
- CTCCCTCTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCTCTCCCTCTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2062898267
seq_region_name: 17
source: dbSNP
start: 73388812
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388813
feature_type: variation
id: rs1599512315
seq_region_name: 17
source: dbSNP
start: 73388813
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388814
feature_type: variation
id: rs2062898317
seq_region_name: 17
source: dbSNP
start: 73388814
strand: 1
-
alleles:
- CCCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs2062898358
seq_region_name: 17
source: dbSNP
start: 73388814
strand: 1
-
alleles:
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- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388814
feature_type: variation
id: rs758405988
seq_region_name: 17
source: dbSNP
start: 73388815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388815
feature_type: variation
id: rs201700715
seq_region_name: 17
source: dbSNP
start: 73388815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs1568377576
seq_region_name: 17
source: dbSNP
start: 73388815
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388822
feature_type: variation
id: rs1308997196
seq_region_name: 17
source: dbSNP
start: 73388815
strand: 1
-
alleles:
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- C
- CTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388820
feature_type: variation
id: rs2062898584
seq_region_name: 17
source: dbSNP
start: 73388816
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388817
feature_type: variation
id: rs200401165
seq_region_name: 17
source: dbSNP
start: 73388817
strand: 1
-
alleles:
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- TC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388824
feature_type: variation
id: rs2062898691
seq_region_name: 17
source: dbSNP
start: 73388817
strand: 1
-
alleles:
- "-"
- TCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388817
feature_type: variation
id: rs2062898736
seq_region_name: 17
source: dbSNP
start: 73388818
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs201155543
seq_region_name: 17
source: dbSNP
start: 73388818
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs746565305
seq_region_name: 17
source: dbSNP
start: 73388818
strand: 1
-
alleles:
- CTCCT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388822
feature_type: variation
id: rs2062898878
seq_region_name: 17
source: dbSNP
start: 73388818
strand: 1
-
alleles:
- "-"
- CT
- CTTCCTTCCCTCCCTCTCCT
- CTTCCTTCCTTCCCTCCCTCTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388818
feature_type: variation
id: rs1568377581
seq_region_name: 17
source: dbSNP
start: 73388819
strand: 1
-
alleles:
- TCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCCTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCTCCTTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs1568377583
seq_region_name: 17
source: dbSNP
start: 73388819
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCC
- TCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCTTCC
- TCCTTCCTTCCTTCCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388837
feature_type: variation
id: rs140671690
seq_region_name: 17
source: dbSNP
start: 73388819
strand: 1
-
alleles:
- TCCTTCCTTCCTTCCTTCCC
- TCCTTCCTTCCTTCCTTCCCTCCCTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCTTCCTTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs1568377587
seq_region_name: 17
source: dbSNP
start: 73388819
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388820
feature_type: variation
id: rs1358324509
seq_region_name: 17
source: dbSNP
start: 73388820
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388821
feature_type: variation
id: rs12951095
seq_region_name: 17
source: dbSNP
start: 73388821
strand: 1
-
alleles:
- CTT
- CTTTCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388823
feature_type: variation
id: rs2062899262
seq_region_name: 17
source: dbSNP
start: 73388821
strand: 1
-
alleles:
- CTTCCTTCCTTCC
- CTTCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2062899299
seq_region_name: 17
source: dbSNP
start: 73388821
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388822
feature_type: variation
id: rs2062899328
seq_region_name: 17
source: dbSNP
start: 73388822
strand: 1
-
alleles:
- TCC
- TCCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388825
feature_type: variation
id: rs1568377593
seq_region_name: 17
source: dbSNP
start: 73388823
strand: 1
-
alleles:
- TCCTTCCTTCC
- TCCTTCCTTCCCTCCCTCCTTCCTTCC
- TCCTTCCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2062899373
seq_region_name: 17
source: dbSNP
start: 73388823
strand: 1
-
alleles:
- CCTTCC
- CCTTCCCTCCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTACCTTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2062899400
seq_region_name: 17
source: dbSNP
start: 73388828
strand: 1
-
alleles:
- TTC
- TTCTTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388832
feature_type: variation
id: rs2062899428
seq_region_name: 17
source: dbSNP
start: 73388830
strand: 1
-
alleles:
- TTCCTTCCCCCCTCCTTTCCTTTTCTTTC
- TTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388858
feature_type: variation
id: rs2145491750
seq_region_name: 17
source: dbSNP
start: 73388830
strand: 1
-
alleles:
- TCC
- TCCCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2062899473
seq_region_name: 17
source: dbSNP
start: 73388831
strand: 1
-
alleles:
- TCCTTCCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs1436183252
seq_region_name: 17
source: dbSNP
start: 73388831
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388833
feature_type: variation
id: rs2062899552
seq_region_name: 17
source: dbSNP
start: 73388832
strand: 1
-
alleles:
- CTT
- CTTTCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388835
feature_type: variation
id: rs2062899593
seq_region_name: 17
source: dbSNP
start: 73388833
strand: 1
-
alleles:
- CTTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388836
feature_type: variation
id: rs1271179961
seq_region_name: 17
source: dbSNP
start: 73388833
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388834
feature_type: variation
id: rs199591018
seq_region_name: 17
source: dbSNP
start: 73388834
strand: 1
-
alleles:
- TTCCCCCCTCCTTTCCTTTTCTTTCTCCCTCTCTTTT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388870
feature_type: variation
id: rs2062899724
seq_region_name: 17
source: dbSNP
start: 73388834
strand: 1
-
alleles:
- "-"
- CCCTCCTTCCTTCCTTCCCTCCCTCTCCTTCCTTCCTTCCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388834
feature_type: variation
id: rs2062899766
seq_region_name: 17
source: dbSNP
start: 73388835
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388836
feature_type: variation
id: rs2062899802
seq_region_name: 17
source: dbSNP
start: 73388836
strand: 1
-
alleles:
- CC
- CCTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388837
feature_type: variation
id: rs1568377611
seq_region_name: 17
source: dbSNP
start: 73388836
strand: 1
-
alleles:
- CCCCCC
- CCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388841
feature_type: variation
id: rs1420186465
seq_region_name: 17
source: dbSNP
start: 73388836
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388837
feature_type: variation
id: rs1382140649
seq_region_name: 17
source: dbSNP
start: 73388837
strand: 1
-
alleles:
- C
- CTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388837
feature_type: variation
id: rs1599512409
seq_region_name: 17
source: dbSNP
start: 73388837
strand: 1
-
alleles:
- "-"
- T
- TT
- TTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388837
feature_type: variation
id: rs2062899999
seq_region_name: 17
source: dbSNP
start: 73388838
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs1278141214
seq_region_name: 17
source: dbSNP
start: 73388838
strand: 1
-
alleles:
- "-"
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388838
feature_type: variation
id: rs1185480961
seq_region_name: 17
source: dbSNP
start: 73388839
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388839
feature_type: variation
id: rs1335479745
seq_region_name: 17
source: dbSNP
start: 73388839
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388840
feature_type: variation
id: rs2062900158
seq_region_name: 17
source: dbSNP
start: 73388840
strand: 1
-
alleles:
- CCTCCT
- CCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388845
feature_type: variation
id: rs2062900209
seq_region_name: 17
source: dbSNP
start: 73388840
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388841
feature_type: variation
id: rs2145491866
seq_region_name: 17
source: dbSNP
start: 73388841
strand: 1
-
alleles:
- CTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388843
feature_type: variation
id: rs1423378195
seq_region_name: 17
source: dbSNP
start: 73388841
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388842
feature_type: variation
id: rs2062900275
seq_region_name: 17
source: dbSNP
start: 73388842
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388843
feature_type: variation
id: rs1215672407
seq_region_name: 17
source: dbSNP
start: 73388843
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388844
feature_type: variation
id: rs1257117315
seq_region_name: 17
source: dbSNP
start: 73388843
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388844
feature_type: variation
id: rs1485024620
seq_region_name: 17
source: dbSNP
start: 73388844
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388845
feature_type: variation
id: rs1451289377
seq_region_name: 17
source: dbSNP
start: 73388845
strand: 1
-
alleles:
- TTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388847
feature_type: variation
id: rs1287961495
seq_region_name: 17
source: dbSNP
start: 73388845
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388846
feature_type: variation
id: rs2062900507
seq_region_name: 17
source: dbSNP
start: 73388846
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388847
feature_type: variation
id: rs1216228703
seq_region_name: 17
source: dbSNP
start: 73388847
strand: 1
-
alleles:
- TTTCTTTCT
- T
- TTTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388859
feature_type: variation
id: rs1217848186
seq_region_name: 17
source: dbSNP
start: 73388851
strand: 1
-
alleles:
- "-"
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388851
feature_type: variation
id: rs1243686781
seq_region_name: 17
source: dbSNP
start: 73388852
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388852
feature_type: variation
id: rs1474310716
seq_region_name: 17
source: dbSNP
start: 73388852
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388853
feature_type: variation
id: rs1192766328
seq_region_name: 17
source: dbSNP
start: 73388853
strand: 1
-
alleles:
- TCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388855
feature_type: variation
id: rs1356433744
seq_region_name: 17
source: dbSNP
start: 73388853
strand: 1
-
alleles:
- TTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388857
feature_type: variation
id: rs1418524484
seq_region_name: 17
source: dbSNP
start: 73388855
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388856
feature_type: variation
id: rs1290285548
seq_region_name: 17
source: dbSNP
start: 73388856
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388857
feature_type: variation
id: rs1475873609
seq_region_name: 17
source: dbSNP
start: 73388857
strand: 1
-
alleles:
- CTCCCTC
- CTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388864
feature_type: variation
id: rs2062900746
seq_region_name: 17
source: dbSNP
start: 73388858
strand: 1
-
alleles:
- CTCTCT
- CTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388867
feature_type: variation
id: rs200219197
seq_region_name: 17
source: dbSNP
start: 73388862
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388863
feature_type: variation
id: rs1339438758
seq_region_name: 17
source: dbSNP
start: 73388863
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388865
feature_type: variation
id: rs1389531569
seq_region_name: 17
source: dbSNP
start: 73388865
strand: 1
-
alleles:
- TCTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388868
feature_type: variation
id: rs2062900846
seq_region_name: 17
source: dbSNP
start: 73388865
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388866
feature_type: variation
id: rs1599512489
seq_region_name: 17
source: dbSNP
start: 73388866
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388867
feature_type: variation
id: rs1400997951
seq_region_name: 17
source: dbSNP
start: 73388867
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388868
feature_type: variation
id: rs1312823134
seq_region_name: 17
source: dbSNP
start: 73388868
strand: 1
-
alleles:
- TCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388873
feature_type: variation
id: rs2145492020
seq_region_name: 17
source: dbSNP
start: 73388870
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388871
feature_type: variation
id: rs1338001922
seq_region_name: 17
source: dbSNP
start: 73388871
strand: 1
-
alleles:
- CTCCCTCC
- CTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388878
feature_type: variation
id: rs1397363582
seq_region_name: 17
source: dbSNP
start: 73388871
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388876
feature_type: variation
id: rs2062900993
seq_region_name: 17
source: dbSNP
start: 73388876
strand: 1
-
alleles:
- TCCTTC
- TC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388881
feature_type: variation
id: rs2062901018
seq_region_name: 17
source: dbSNP
start: 73388876
strand: 1
-
alleles:
- TCCTTCTCTTCCTTCTC
- TCCTTCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388892
feature_type: variation
id: rs1319376897
seq_region_name: 17
source: dbSNP
start: 73388876
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388878
feature_type: variation
id: rs2062901083
seq_region_name: 17
source: dbSNP
start: 73388878
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388881
feature_type: variation
id: rs2062901118
seq_region_name: 17
source: dbSNP
start: 73388881
strand: 1
-
alleles:
- CTCTTCCTTCTCCCTC
- CTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388896
feature_type: variation
id: rs2062901148
seq_region_name: 17
source: dbSNP
start: 73388881
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062901291
seq_region_name: 17
source: dbSNP
start: 73388890
strand: 1
-
alleles:
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- CTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388891
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388892
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388895
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388896
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388897
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs899878066
seq_region_name: 17
source: dbSNP
start: 73388899
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs996869584
seq_region_name: 17
source: dbSNP
start: 73388900
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388901
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388902
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs958011024
seq_region_name: 17
source: dbSNP
start: 73388903
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388904
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388911
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388911
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388913
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388913
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73388913
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388913
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145492248
seq_region_name: 17
source: dbSNP
start: 73388914
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388915
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1355889969
seq_region_name: 17
source: dbSNP
start: 73388915
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388916
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388916
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568377695
seq_region_name: 17
source: dbSNP
start: 73388917
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1198632983
seq_region_name: 17
source: dbSNP
start: 73388917
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062902175
seq_region_name: 17
source: dbSNP
start: 73388917
strand: 1
-
alleles:
- TTTCCCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062902199
seq_region_name: 17
source: dbSNP
start: 73388917
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388919
feature_type: variation
id: rs1452657961
seq_region_name: 17
source: dbSNP
start: 73388919
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062902242
seq_region_name: 17
source: dbSNP
start: 73388920
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388925
feature_type: variation
id: rs1184775836
seq_region_name: 17
source: dbSNP
start: 73388920
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388921
feature_type: variation
id: rs1456117442
seq_region_name: 17
source: dbSNP
start: 73388921
strand: 1
-
alleles:
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- CCCCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388953
feature_type: variation
id: rs1286616238
seq_region_name: 17
source: dbSNP
start: 73388921
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388922
feature_type: variation
id: rs1256871383
seq_region_name: 17
source: dbSNP
start: 73388922
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388958
feature_type: variation
id: rs2062902343
seq_region_name: 17
source: dbSNP
start: 73388922
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388923
feature_type: variation
id: rs2062902363
seq_region_name: 17
source: dbSNP
start: 73388923
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388925
feature_type: variation
id: rs1218797816
seq_region_name: 17
source: dbSNP
start: 73388925
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388926
feature_type: variation
id: rs1487162097
seq_region_name: 17
source: dbSNP
start: 73388926
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1319585708
seq_region_name: 17
source: dbSNP
start: 73388927
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388928
feature_type: variation
id: rs2145492347
seq_region_name: 17
source: dbSNP
start: 73388928
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062902450
seq_region_name: 17
source: dbSNP
start: 73388929
strand: 1
-
alleles:
- CCTCCCCTCCCTTTCCCTTCCCCCTCCCCTCCCCTCTCCTCCCTTCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145492361
seq_region_name: 17
source: dbSNP
start: 73388929
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388931
feature_type: variation
id: rs982648267
seq_region_name: 17
source: dbSNP
start: 73388931
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388932
feature_type: variation
id: rs2062902484
seq_region_name: 17
source: dbSNP
start: 73388932
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388935
feature_type: variation
id: rs1272818536
seq_region_name: 17
source: dbSNP
start: 73388932
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388952
feature_type: variation
id: rs2062902535
seq_region_name: 17
source: dbSNP
start: 73388932
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388933
feature_type: variation
id: rs181711959
seq_region_name: 17
source: dbSNP
start: 73388933
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388935
feature_type: variation
id: rs1599512677
seq_region_name: 17
source: dbSNP
start: 73388935
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388936
feature_type: variation
id: rs926411059
seq_region_name: 17
source: dbSNP
start: 73388936
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388940
feature_type: variation
id: rs2062902614
seq_region_name: 17
source: dbSNP
start: 73388940
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388942
feature_type: variation
id: rs1599512685
seq_region_name: 17
source: dbSNP
start: 73388942
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388946
feature_type: variation
id: rs2145492422
seq_region_name: 17
source: dbSNP
start: 73388946
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388947
feature_type: variation
id: rs1232312143
seq_region_name: 17
source: dbSNP
start: 73388947
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388948
feature_type: variation
id: rs1215656095
seq_region_name: 17
source: dbSNP
start: 73388948
strand: 1
-
alleles:
- CCCCTCCCCTCCCCTC
- CCCCTCCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388964
feature_type: variation
id: rs2062902710
seq_region_name: 17
source: dbSNP
start: 73388949
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388951
feature_type: variation
id: rs2062902730
seq_region_name: 17
source: dbSNP
start: 73388951
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388953
feature_type: variation
id: rs959354199
seq_region_name: 17
source: dbSNP
start: 73388953
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388956
feature_type: variation
id: rs1258111424
seq_region_name: 17
source: dbSNP
start: 73388956
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388958
feature_type: variation
id: rs1599512698
seq_region_name: 17
source: dbSNP
start: 73388958
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388960
feature_type: variation
id: rs2062902823
seq_region_name: 17
source: dbSNP
start: 73388960
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388961
feature_type: variation
id: rs1794209129
seq_region_name: 17
source: dbSNP
start: 73388961
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388962
feature_type: variation
id: rs2062902846
seq_region_name: 17
source: dbSNP
start: 73388962
strand: 1
-
alleles:
- CTCTC
- CTCTCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388966
feature_type: variation
id: rs2062902869
seq_region_name: 17
source: dbSNP
start: 73388962
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73388963
feature_type: variation
id: rs1599512709
seq_region_name: 17
source: dbSNP
start: 73388963
strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388995
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73388996
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389005
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389011
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389012
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389013
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs894627203
seq_region_name: 17
source: dbSNP
start: 73389019
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2062903998
seq_region_name: 17
source: dbSNP
start: 73389025
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389048
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389049
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389050
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389051
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs906302440
seq_region_name: 17
source: dbSNP
start: 73389053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062904170
seq_region_name: 17
source: dbSNP
start: 73389059
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389061
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062904233
seq_region_name: 17
source: dbSNP
start: 73389064
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062904255
seq_region_name: 17
source: dbSNP
start: 73389066
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145492786
seq_region_name: 17
source: dbSNP
start: 73389067
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145492787
seq_region_name: 17
source: dbSNP
start: 73389068
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs552595637
seq_region_name: 17
source: dbSNP
start: 73389069
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1292044275
seq_region_name: 17
source: dbSNP
start: 73389070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389074
feature_type: variation
id: rs564419761
seq_region_name: 17
source: dbSNP
start: 73389074
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389075
feature_type: variation
id: rs2062904349
seq_region_name: 17
source: dbSNP
start: 73389075
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1699219609
seq_region_name: 17
source: dbSNP
start: 73389076
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389082
feature_type: variation
id: rs2062904370
seq_region_name: 17
source: dbSNP
start: 73389082
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389086
feature_type: variation
id: rs2145492841
seq_region_name: 17
source: dbSNP
start: 73389084
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389086
feature_type: variation
id: rs2062904401
seq_region_name: 17
source: dbSNP
start: 73389086
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389087
feature_type: variation
id: rs2062904425
seq_region_name: 17
source: dbSNP
start: 73389087
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389091
feature_type: variation
id: rs2145492855
seq_region_name: 17
source: dbSNP
start: 73389088
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389091
feature_type: variation
id: rs2062904445
seq_region_name: 17
source: dbSNP
start: 73389091
strand: 1
-
alleles:
- AAA
- AAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389094
feature_type: variation
id: rs2062904474
seq_region_name: 17
source: dbSNP
start: 73389092
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389093
feature_type: variation
id: rs2062904487
seq_region_name: 17
source: dbSNP
start: 73389093
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389094
feature_type: variation
id: rs2145492874
seq_region_name: 17
source: dbSNP
start: 73389094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs907072034
seq_region_name: 17
source: dbSNP
start: 73389097
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389098
feature_type: variation
id: rs2062904538
seq_region_name: 17
source: dbSNP
start: 73389098
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389099
feature_type: variation
id: rs2145492885
seq_region_name: 17
source: dbSNP
start: 73389099
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389100
feature_type: variation
id: rs1599512880
seq_region_name: 17
source: dbSNP
start: 73389100
strand: 1
-
alleles:
- "-"
- CCCCCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389100
feature_type: variation
id: rs2145492898
seq_region_name: 17
source: dbSNP
start: 73389101
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389102
feature_type: variation
id: rs1442657694
seq_region_name: 17
source: dbSNP
start: 73389102
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389103
feature_type: variation
id: rs2062904600
seq_region_name: 17
source: dbSNP
start: 73389103
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389109
feature_type: variation
id: rs1467347020
seq_region_name: 17
source: dbSNP
start: 73389109
strand: 1
-
alleles:
- CAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389111
feature_type: variation
id: rs2145492916
seq_region_name: 17
source: dbSNP
start: 73389109
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389113
feature_type: variation
id: rs2145492918
seq_region_name: 17
source: dbSNP
start: 73389113
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389114
feature_type: variation
id: rs2062904655
seq_region_name: 17
source: dbSNP
start: 73389113
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389114
feature_type: variation
id: rs2145492930
seq_region_name: 17
source: dbSNP
start: 73389114
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389115
feature_type: variation
id: rs2062904682
seq_region_name: 17
source: dbSNP
start: 73389115
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389116
feature_type: variation
id: rs1599512895
seq_region_name: 17
source: dbSNP
start: 73389116
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389117
feature_type: variation
id: rs2062904724
seq_region_name: 17
source: dbSNP
start: 73389117
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389119
feature_type: variation
id: rs547378064
seq_region_name: 17
source: dbSNP
start: 73389119
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389120
feature_type: variation
id: rs1352865519
seq_region_name: 17
source: dbSNP
start: 73389120
strand: 1
-
alleles:
- CCTCGGCCTC
- CCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389129
feature_type: variation
id: rs2062904801
seq_region_name: 17
source: dbSNP
start: 73389120
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389121
feature_type: variation
id: rs1286718440
seq_region_name: 17
source: dbSNP
start: 73389121
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389123
feature_type: variation
id: rs957749028
seq_region_name: 17
source: dbSNP
start: 73389123
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389124
feature_type: variation
id: rs1011224789
seq_region_name: 17
source: dbSNP
start: 73389124
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389127
feature_type: variation
id: rs1443061288
seq_region_name: 17
source: dbSNP
start: 73389127
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389132
feature_type: variation
id: rs78047814
seq_region_name: 17
source: dbSNP
start: 73389132
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389143
feature_type: variation
id: rs1599512930
seq_region_name: 17
source: dbSNP
start: 73389143
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389144
feature_type: variation
id: rs2062904998
seq_region_name: 17
source: dbSNP
start: 73389144
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389146
feature_type: variation
id: rs1448967148
seq_region_name: 17
source: dbSNP
start: 73389146
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389147
feature_type: variation
id: rs1342520550
seq_region_name: 17
source: dbSNP
start: 73389147
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389148
feature_type: variation
id: rs2062905041
seq_region_name: 17
source: dbSNP
start: 73389148
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389150
feature_type: variation
id: rs2062905070
seq_region_name: 17
source: dbSNP
start: 73389150
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389151
feature_type: variation
id: rs2062905095
seq_region_name: 17
source: dbSNP
start: 73389151
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389154
feature_type: variation
id: rs1351842394
seq_region_name: 17
source: dbSNP
start: 73389154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389155
feature_type: variation
id: rs2145493021
seq_region_name: 17
source: dbSNP
start: 73389155
strand: 1
-
alleles:
- CACCACCAC
- CACCACCACCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389163
feature_type: variation
id: rs1021720272
seq_region_name: 17
source: dbSNP
start: 73389155
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389156
feature_type: variation
id: rs2145493039
seq_region_name: 17
source: dbSNP
start: 73389156
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389162
feature_type: variation
id: rs1399835792
seq_region_name: 17
source: dbSNP
start: 73389162
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389164
feature_type: variation
id: rs1361718926
seq_region_name: 17
source: dbSNP
start: 73389164
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389164
feature_type: variation
id: rs2145493052
seq_region_name: 17
source: dbSNP
start: 73389164
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389165
feature_type: variation
id: rs546850157
seq_region_name: 17
source: dbSNP
start: 73389165
strand: 1
-
alleles:
- CCTGGCTGATATTCCT
- CCTGGCTGATATTCCTGGCTGATATTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389180
feature_type: variation
id: rs2062905220
seq_region_name: 17
source: dbSNP
start: 73389165
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389168
feature_type: variation
id: rs1404105545
seq_region_name: 17
source: dbSNP
start: 73389168
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389169
feature_type: variation
id: rs775172761
seq_region_name: 17
source: dbSNP
start: 73389169
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389171
feature_type: variation
id: rs2145493081
seq_region_name: 17
source: dbSNP
start: 73389171
strand: 1
-
alleles:
- TGAT
- TGATGAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389174
feature_type: variation
id: rs2062905282
seq_region_name: 17
source: dbSNP
start: 73389171
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389172
feature_type: variation
id: rs2062905316
seq_region_name: 17
source: dbSNP
start: 73389172
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389179
feature_type: variation
id: rs1162156226
seq_region_name: 17
source: dbSNP
start: 73389179
strand: 1
-
alleles:
- CTTTCTTT
- CTTT
- CTTTCTTTCTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389186
feature_type: variation
id: rs1239124187
seq_region_name: 17
source: dbSNP
start: 73389179
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389180
feature_type: variation
id: rs964351534
seq_region_name: 17
source: dbSNP
start: 73389180
strand: 1
-
alleles:
- TTTCTTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389187
feature_type: variation
id: rs1472902475
seq_region_name: 17
source: dbSNP
start: 73389180
strand: 1
-
alleles:
- TCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389184
feature_type: variation
id: rs143990147
seq_region_name: 17
source: dbSNP
start: 73389182
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389183
feature_type: variation
id: rs77236080
seq_region_name: 17
source: dbSNP
start: 73389183
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389184
feature_type: variation
id: rs2078740807
seq_region_name: 17
source: dbSNP
start: 73389184
strand: 1
-
alleles:
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389203
feature_type: variation
id: rs61085516
seq_region_name: 17
source: dbSNP
start: 73389184
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389185
feature_type: variation
id: rs2062905649
seq_region_name: 17
source: dbSNP
start: 73389185
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389186
feature_type: variation
id: rs1291017481
seq_region_name: 17
source: dbSNP
start: 73389186
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389187
feature_type: variation
id: rs568258732
seq_region_name: 17
source: dbSNP
start: 73389187
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389188
feature_type: variation
id: rs535265720
seq_region_name: 17
source: dbSNP
start: 73389188
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389189
feature_type: variation
id: rs1437869966
seq_region_name: 17
source: dbSNP
start: 73389189
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389190
feature_type: variation
id: rs2062905770
seq_region_name: 17
source: dbSNP
start: 73389190
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389198
feature_type: variation
id: rs1183388540
seq_region_name: 17
source: dbSNP
start: 73389198
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389202
feature_type: variation
id: rs1405501181
seq_region_name: 17
source: dbSNP
start: 73389202
strand: 1
-
alleles:
- TG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389204
feature_type: variation
id: rs1235959095
seq_region_name: 17
source: dbSNP
start: 73389203
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389204
feature_type: variation
id: rs1158402454
seq_region_name: 17
source: dbSNP
start: 73389204
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389204
feature_type: variation
id: rs1168005444
seq_region_name: 17
source: dbSNP
start: 73389204
strand: 1
-
alleles:
- GAGA
- GA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389207
feature_type: variation
id: rs1477298646
seq_region_name: 17
source: dbSNP
start: 73389204
strand: 1
-
alleles:
- GAGACGG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389210
feature_type: variation
id: rs1438765294
seq_region_name: 17
source: dbSNP
start: 73389204
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389205
feature_type: variation
id: rs1188081259
seq_region_name: 17
source: dbSNP
start: 73389205
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389205
feature_type: variation
id: rs1396005127
seq_region_name: 17
source: dbSNP
start: 73389205
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389208
feature_type: variation
id: rs1467904542
seq_region_name: 17
source: dbSNP
start: 73389208
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389209
feature_type: variation
id: rs1171294945
seq_region_name: 17
source: dbSNP
start: 73389209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389210
feature_type: variation
id: rs2062906030
seq_region_name: 17
source: dbSNP
start: 73389210
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389211
feature_type: variation
id: rs1222385857
seq_region_name: 17
source: dbSNP
start: 73389211
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389212
feature_type: variation
id: rs1402145017
seq_region_name: 17
source: dbSNP
start: 73389212
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389214
feature_type: variation
id: rs2062906099
seq_region_name: 17
source: dbSNP
start: 73389214
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389215
feature_type: variation
id: rs1599513098
seq_region_name: 17
source: dbSNP
start: 73389215
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389216
feature_type: variation
id: rs2062906140
seq_region_name: 17
source: dbSNP
start: 73389216
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389218
feature_type: variation
id: rs1410581521
seq_region_name: 17
source: dbSNP
start: 73389218
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389219
feature_type: variation
id: rs2062906199
seq_region_name: 17
source: dbSNP
start: 73389219
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389221
feature_type: variation
id: rs2062906221
seq_region_name: 17
source: dbSNP
start: 73389221
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389222
feature_type: variation
id: rs2062906237
seq_region_name: 17
source: dbSNP
start: 73389222
strand: 1
-
alleles:
- AGCCCAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389228
feature_type: variation
id: rs760363832
seq_region_name: 17
source: dbSNP
start: 73389222
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389223
feature_type: variation
id: rs1599513107
seq_region_name: 17
source: dbSNP
start: 73389223
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389224
feature_type: variation
id: rs1198187660
seq_region_name: 17
source: dbSNP
start: 73389224
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389227
feature_type: variation
id: rs1599513119
seq_region_name: 17
source: dbSNP
start: 73389227
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389228
feature_type: variation
id: rs1599513125
seq_region_name: 17
source: dbSNP
start: 73389228
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389229
feature_type: variation
id: rs2062906328
seq_region_name: 17
source: dbSNP
start: 73389229
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389234
feature_type: variation
id: rs1599513131
seq_region_name: 17
source: dbSNP
start: 73389234
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389235
feature_type: variation
id: rs1374951469
seq_region_name: 17
source: dbSNP
start: 73389235
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389236
feature_type: variation
id: rs2062906410
seq_region_name: 17
source: dbSNP
start: 73389236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389238
feature_type: variation
id: rs2062906434
seq_region_name: 17
source: dbSNP
start: 73389238
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389240
feature_type: variation
id: rs1446396734
seq_region_name: 17
source: dbSNP
start: 73389240
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389246
feature_type: variation
id: rs934186456
seq_region_name: 17
source: dbSNP
start: 73389246
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389248
feature_type: variation
id: rs1599513157
seq_region_name: 17
source: dbSNP
start: 73389248
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389252
feature_type: variation
id: rs1372828505
seq_region_name: 17
source: dbSNP
start: 73389252
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389253
feature_type: variation
id: rs1367496121
seq_region_name: 17
source: dbSNP
start: 73389253
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389258
feature_type: variation
id: rs2062906573
seq_region_name: 17
source: dbSNP
start: 73389258
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389262
feature_type: variation
id: rs1230837269
seq_region_name: 17
source: dbSNP
start: 73389262
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389269
feature_type: variation
id: rs964216931
seq_region_name: 17
source: dbSNP
start: 73389269
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389270
feature_type: variation
id: rs1395960936
seq_region_name: 17
source: dbSNP
start: 73389270
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389272
feature_type: variation
id: rs976583003
seq_region_name: 17
source: dbSNP
start: 73389272
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389274
feature_type: variation
id: rs1029718451
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389432
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389435
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389444
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389448
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1274640006
seq_region_name: 17
source: dbSNP
start: 73389452
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389454
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389459
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389462
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389463
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389465
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389466
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389468
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145493799
seq_region_name: 17
source: dbSNP
start: 73389469
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1487550892
seq_region_name: 17
source: dbSNP
start: 73389470
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062908541
seq_region_name: 17
source: dbSNP
start: 73389471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389473
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389474
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389475
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389477
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389479
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389480
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062908830
seq_region_name: 17
source: dbSNP
start: 73389481
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293597565
seq_region_name: 17
source: dbSNP
start: 73389482
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389485
feature_type: variation
id: rs2062908902
seq_region_name: 17
source: dbSNP
start: 73389485
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389486
feature_type: variation
id: rs2062908941
seq_region_name: 17
source: dbSNP
start: 73389486
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73389492
feature_type: variation
id: rs982856286
seq_region_name: 17
source: dbSNP
start: 73389492
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389680
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73389710
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389712
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389714
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389720
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73389722
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389726
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389728
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73389734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389736
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389743
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389744
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73389749
strand: 1
-
alleles:
- TTAATTAATTAATTAATT
- TTAATTAATTAATT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1411875274
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73389959
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73390144
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73390148
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73390156
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73390162
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390163
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390165
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390170
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390171
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73390175
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seq_region_name: 17
source: dbSNP
start: 73390175
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390179
feature_type: variation
id: rs2145495344
seq_region_name: 17
source: dbSNP
start: 73390179
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390187
feature_type: variation
id: rs2145495347
seq_region_name: 17
source: dbSNP
start: 73390187
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390196
feature_type: variation
id: rs2062915192
seq_region_name: 17
source: dbSNP
start: 73390196
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390198
feature_type: variation
id: rs115743912
seq_region_name: 17
source: dbSNP
start: 73390198
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390199
feature_type: variation
id: rs1599514387
seq_region_name: 17
source: dbSNP
start: 73390199
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390204
feature_type: variation
id: rs2062915275
seq_region_name: 17
source: dbSNP
start: 73390204
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390205
feature_type: variation
id: rs1022334745
seq_region_name: 17
source: dbSNP
start: 73390205
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390207
feature_type: variation
id: rs2145495383
seq_region_name: 17
source: dbSNP
start: 73390207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390209
feature_type: variation
id: rs928709157
seq_region_name: 17
source: dbSNP
start: 73390209
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390211
feature_type: variation
id: rs2145495394
seq_region_name: 17
source: dbSNP
start: 73390211
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390214
feature_type: variation
id: rs2062915349
seq_region_name: 17
source: dbSNP
start: 73390214
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390217
feature_type: variation
id: rs2145495404
seq_region_name: 17
source: dbSNP
start: 73390217
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390219
feature_type: variation
id: rs1313476302
seq_region_name: 17
source: dbSNP
start: 73390219
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390221
feature_type: variation
id: rs2062915397
seq_region_name: 17
source: dbSNP
start: 73390221
strand: 1
-
alleles:
- CACT
- CACTCACT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390231
feature_type: variation
id: rs1436486023
seq_region_name: 17
source: dbSNP
start: 73390228
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390229
feature_type: variation
id: rs2062915424
seq_region_name: 17
source: dbSNP
start: 73390229
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390231
feature_type: variation
id: rs2062915450
seq_region_name: 17
source: dbSNP
start: 73390231
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390237
feature_type: variation
id: rs1362181955
seq_region_name: 17
source: dbSNP
start: 73390237
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390238
feature_type: variation
id: rs777773613
seq_region_name: 17
source: dbSNP
start: 73390238
strand: 1
-
alleles:
- CCCCCCC
- CCCCCC
- CCCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390244
feature_type: variation
id: rs767147221
seq_region_name: 17
source: dbSNP
start: 73390238
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390239
feature_type: variation
id: rs1444350295
seq_region_name: 17
source: dbSNP
start: 73390239
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390241
feature_type: variation
id: rs1440200128
seq_region_name: 17
source: dbSNP
start: 73390241
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390242
feature_type: variation
id: rs199778648
seq_region_name: 17
source: dbSNP
start: 73390242
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390243
feature_type: variation
id: rs758530672
seq_region_name: 17
source: dbSNP
start: 73390243
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390244
feature_type: variation
id: rs551084384
seq_region_name: 17
source: dbSNP
start: 73390244
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390245
feature_type: variation
id: rs1599514452
seq_region_name: 17
source: dbSNP
start: 73390245
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390245
feature_type: variation
id: rs2062915720
seq_region_name: 17
source: dbSNP
start: 73390245
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390247
feature_type: variation
id: rs1258640240
seq_region_name: 17
source: dbSNP
start: 73390247
strand: 1
-
alleles:
- AGCTG
- AGCTGAGCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390251
feature_type: variation
id: rs752257433
seq_region_name: 17
source: dbSNP
start: 73390247
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390251
feature_type: variation
id: rs777128128
seq_region_name: 17
source: dbSNP
start: 73390251
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390255
feature_type: variation
id: rs748546066
seq_region_name: 17
source: dbSNP
start: 73390255
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390256
feature_type: variation
id: rs1172962024
seq_region_name: 17
source: dbSNP
start: 73390256
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390259
feature_type: variation
id: rs1487576678
seq_region_name: 17
source: dbSNP
start: 73390259
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390261
feature_type: variation
id: rs779184179
seq_region_name: 17
source: dbSNP
start: 73390261
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390264
feature_type: variation
id: rs1432513465
seq_region_name: 17
source: dbSNP
start: 73390264
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390266
feature_type: variation
id: rs762328775
seq_region_name: 17
source: dbSNP
start: 73390266
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390269
feature_type: variation
id: rs1360579650
seq_region_name: 17
source: dbSNP
start: 73390269
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390271
feature_type: variation
id: rs1401371633
seq_region_name: 17
source: dbSNP
start: 73390271
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390274
feature_type: variation
id: rs201321798
seq_region_name: 17
source: dbSNP
start: 73390274
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390275
feature_type: variation
id: rs773900234
seq_region_name: 17
source: dbSNP
start: 73390275
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390276
feature_type: variation
id: rs372627552
seq_region_name: 17
source: dbSNP
start: 73390276
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73390279
feature_type: variation
id: rs1275832400
seq_region_name: 17
source: dbSNP
start: 73390279
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73390280
feature_type: variation
id: rs1159217570
seq_region_name: 17
source: dbSNP
start: 73390280
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73390282
feature_type: variation
id: rs767224773
seq_region_name: 17
source: dbSNP
start: 73390282
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73390284
feature_type: variation
id: rs527300776
seq_region_name: 17
source: dbSNP
start: 73390284
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390293
feature_type: variation
id: rs752368771
seq_region_name: 17
source: dbSNP
start: 73390293
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390294
feature_type: variation
id: rs1354642321
seq_region_name: 17
source: dbSNP
start: 73390294
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390296
feature_type: variation
id: rs1279937439
seq_region_name: 17
source: dbSNP
start: 73390296
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390297
feature_type: variation
id: rs548698767
seq_region_name: 17
source: dbSNP
start: 73390297
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390301
feature_type: variation
id: rs2062916292
seq_region_name: 17
source: dbSNP
start: 73390301
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390303
feature_type: variation
id: rs370091048
seq_region_name: 17
source: dbSNP
start: 73390303
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390304
feature_type: variation
id: rs1259507232
seq_region_name: 17
source: dbSNP
start: 73390304
strand: 1
-
alleles:
- "-"
- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73390306
feature_type: variation
id: rs1599514580
seq_region_name: 17
source: dbSNP
start: 73390307
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390307
feature_type: variation
id: rs1446384076
seq_region_name: 17
source: dbSNP
start: 73390307
strand: 1
-
alleles:
- ACCAAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73390312
feature_type: variation
id: rs2062916453
seq_region_name: 17
source: dbSNP
start: 73390307
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390308
feature_type: variation
id: rs142762724
seq_region_name: 17
source: dbSNP
start: 73390308
strand: 1
-
alleles:
- A
- ATTAAA
- ATTAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73390310
feature_type: variation
id: rs1379123417
seq_region_name: 17
source: dbSNP
start: 73390310
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390311
feature_type: variation
id: rs1599514607
seq_region_name: 17
source: dbSNP
start: 73390311
strand: 1
-
alleles:
- GGCCTCGG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73390319
feature_type: variation
id: rs2145495712
seq_region_name: 17
source: dbSNP
start: 73390312
strand: 1
-
alleles:
- GGCCTCGGC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73390320
feature_type: variation
id: rs1452398406
seq_region_name: 17
source: dbSNP
start: 73390312
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390313
feature_type: variation
id: rs921787451
seq_region_name: 17
source: dbSNP
start: 73390313
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390314
feature_type: variation
id: rs753848193
seq_region_name: 17
source: dbSNP
start: 73390314
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390317
feature_type: variation
id: rs757302689
seq_region_name: 17
source: dbSNP
start: 73390317
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390318
feature_type: variation
id: rs374363485
seq_region_name: 17
source: dbSNP
start: 73390318
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390319
feature_type: variation
id: rs755179963
seq_region_name: 17
source: dbSNP
start: 73390319
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390320
feature_type: variation
id: rs2145495781
seq_region_name: 17
source: dbSNP
start: 73390320
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390329
feature_type: variation
id: rs144939655
seq_region_name: 17
source: dbSNP
start: 73390329
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390332
feature_type: variation
id: rs781575210
seq_region_name: 17
source: dbSNP
start: 73390332
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390333
feature_type: variation
id: rs770223871
seq_region_name: 17
source: dbSNP
start: 73390333
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390335
feature_type: variation
id: rs778037753
seq_region_name: 17
source: dbSNP
start: 73390335
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390338
feature_type: variation
id: rs1302873867
seq_region_name: 17
source: dbSNP
start: 73390338
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390339
feature_type: variation
id: rs1163126033
seq_region_name: 17
source: dbSNP
start: 73390339
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390340
feature_type: variation
id: rs749780898
seq_region_name: 17
source: dbSNP
start: 73390340
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73390341
feature_type: variation
id: rs771484029
seq_region_name: 17
source: dbSNP
start: 73390341
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390344
feature_type: variation
id: rs1599514692
seq_region_name: 17
source: dbSNP
start: 73390344
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390346
feature_type: variation
id: rs2145495853
seq_region_name: 17
source: dbSNP
start: 73390346
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390347
feature_type: variation
id: rs773847301
seq_region_name: 17
source: dbSNP
start: 73390347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390350
feature_type: variation
id: rs759051308
seq_region_name: 17
source: dbSNP
start: 73390350
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390351
feature_type: variation
id: rs370430999
seq_region_name: 17
source: dbSNP
start: 73390351
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390352
feature_type: variation
id: rs368286974
seq_region_name: 17
source: dbSNP
start: 73390352
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390356
feature_type: variation
id: rs2062917202
seq_region_name: 17
source: dbSNP
start: 73390356
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390358
feature_type: variation
id: rs138821148
seq_region_name: 17
source: dbSNP
start: 73390358
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390359
feature_type: variation
id: rs763920594
seq_region_name: 17
source: dbSNP
start: 73390359
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73390360
feature_type: variation
id: rs1568378436
seq_region_name: 17
source: dbSNP
start: 73390359
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs753628653
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source: dbSNP
start: 73390362
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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consequence_type: missense_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390365
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2062917359
seq_region_name: 17
source: dbSNP
start: 73390367
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs569492221
seq_region_name: 17
source: dbSNP
start: 73390368
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1420524626
seq_region_name: 17
source: dbSNP
start: 73390369
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1156261310
seq_region_name: 17
source: dbSNP
start: 73390370
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390371
feature_type: variation
id: rs1362675363
seq_region_name: 17
source: dbSNP
start: 73390371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs374471476
seq_region_name: 17
source: dbSNP
start: 73390375
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390377
feature_type: variation
id: rs1164325638
seq_region_name: 17
source: dbSNP
start: 73390377
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390378
feature_type: variation
id: rs751628670
seq_region_name: 17
source: dbSNP
start: 73390378
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390381
feature_type: variation
id: rs939718765
seq_region_name: 17
source: dbSNP
start: 73390381
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390383
feature_type: variation
id: rs1460153269
seq_region_name: 17
source: dbSNP
start: 73390383
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390384
feature_type: variation
id: rs2062917635
seq_region_name: 17
source: dbSNP
start: 73390384
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390388
feature_type: variation
id: rs755128780
seq_region_name: 17
source: dbSNP
start: 73390388
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390390
feature_type: variation
id: rs374855753
seq_region_name: 17
source: dbSNP
start: 73390390
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390391
feature_type: variation
id: rs539989751
seq_region_name: 17
source: dbSNP
start: 73390391
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390395
feature_type: variation
id: rs1305194454
seq_region_name: 17
source: dbSNP
start: 73390395
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390397
feature_type: variation
id: rs749718516
seq_region_name: 17
source: dbSNP
start: 73390397
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390400
feature_type: variation
id: rs771361431
seq_region_name: 17
source: dbSNP
start: 73390400
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390403
feature_type: variation
id: rs2062917848
seq_region_name: 17
source: dbSNP
start: 73390403
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390405
feature_type: variation
id: rs1274899035
seq_region_name: 17
source: dbSNP
start: 73390405
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390406
feature_type: variation
id: rs141452799
seq_region_name: 17
source: dbSNP
start: 73390406
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390407
feature_type: variation
id: rs745336235
seq_region_name: 17
source: dbSNP
start: 73390407
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73390408
feature_type: variation
id: rs371257799
seq_region_name: 17
source: dbSNP
start: 73390408
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390409
feature_type: variation
id: rs375846266
seq_region_name: 17
source: dbSNP
start: 73390409
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390410
feature_type: variation
id: rs201007116
seq_region_name: 17
source: dbSNP
start: 73390410
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390411
feature_type: variation
id: rs150858732
seq_region_name: 17
source: dbSNP
start: 73390411
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390414
feature_type: variation
id: rs765214854
seq_region_name: 17
source: dbSNP
start: 73390414
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390419
feature_type: variation
id: rs773310208
seq_region_name: 17
source: dbSNP
start: 73390419
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390422
feature_type: variation
id: rs763023492
seq_region_name: 17
source: dbSNP
start: 73390422
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390423
feature_type: variation
id: rs2062918150
seq_region_name: 17
source: dbSNP
start: 73390423
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390425
feature_type: variation
id: rs767611808
seq_region_name: 17
source: dbSNP
start: 73390425
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390426
feature_type: variation
id: rs1474532540
seq_region_name: 17
source: dbSNP
start: 73390426
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390427
feature_type: variation
id: rs2062918196
seq_region_name: 17
source: dbSNP
start: 73390427
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390430
feature_type: variation
id: rs1164883971
seq_region_name: 17
source: dbSNP
start: 73390430
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390432
feature_type: variation
id: rs752777513
seq_region_name: 17
source: dbSNP
start: 73390432
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390435
feature_type: variation
id: rs756355073
seq_region_name: 17
source: dbSNP
start: 73390435
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390437
feature_type: variation
id: rs764226802
seq_region_name: 17
source: dbSNP
start: 73390437
strand: 1
-
alleles:
- "-"
- TG
- TGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73390437
feature_type: variation
id: rs142302575
seq_region_name: 17
source: dbSNP
start: 73390438
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390438
feature_type: variation
id: rs61752521
seq_region_name: 17
source: dbSNP
start: 73390438
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390440
feature_type: variation
id: rs555457811
seq_region_name: 17
source: dbSNP
start: 73390440
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73390441
feature_type: variation
id: rs1599514964
seq_region_name: 17
source: dbSNP
start: 73390441
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390442
feature_type: variation
id: rs1295223625
seq_region_name: 17
source: dbSNP
start: 73390442
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390444
feature_type: variation
id: rs779354379
seq_region_name: 17
source: dbSNP
start: 73390444
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390445
feature_type: variation
id: rs746345327
seq_region_name: 17
source: dbSNP
start: 73390445
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390446
feature_type: variation
id: rs758881108
seq_region_name: 17
source: dbSNP
start: 73390446
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390447
feature_type: variation
id: rs138263278
seq_region_name: 17
source: dbSNP
start: 73390447
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390448
feature_type: variation
id: rs746572349
seq_region_name: 17
source: dbSNP
start: 73390448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390455
feature_type: variation
id: rs768292999
seq_region_name: 17
source: dbSNP
start: 73390455
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390456
feature_type: variation
id: rs1483388415
seq_region_name: 17
source: dbSNP
start: 73390456
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390457
feature_type: variation
id: rs1212360780
seq_region_name: 17
source: dbSNP
start: 73390457
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390462
feature_type: variation
id: rs776441593
seq_region_name: 17
source: dbSNP
start: 73390462
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390463
feature_type: variation
id: rs1474624250
seq_region_name: 17
source: dbSNP
start: 73390463
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390464
feature_type: variation
id: rs149624554
seq_region_name: 17
source: dbSNP
start: 73390464
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390467
feature_type: variation
id: rs1175644296
seq_region_name: 17
source: dbSNP
start: 73390467
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390469
feature_type: variation
id: rs769678469
seq_region_name: 17
source: dbSNP
start: 73390469
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73390471
feature_type: variation
id: rs2062918898
seq_region_name: 17
source: dbSNP
start: 73390471
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73390480
feature_type: variation
id: rs773188872
seq_region_name: 17
source: dbSNP
start: 73390480
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73390481
feature_type: variation
id: rs1168790383
seq_region_name: 17
source: dbSNP
start: 73390481
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73390484
feature_type: variation
id: rs2062918984
seq_region_name: 17
source: dbSNP
start: 73390484
strand: 1
-
alleles:
- GGAAGGAAG
- GGAAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73390495
feature_type: variation
id: rs765759851
seq_region_name: 17
source: dbSNP
start: 73390487
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73390492
feature_type: variation
id: rs750844489
seq_region_name: 17
source: dbSNP
start: 73390491
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73390495
feature_type: variation
id: rs1021845481
seq_region_name: 17
source: dbSNP
start: 73390495
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73390496
feature_type: variation
id: rs1337275278
seq_region_name: 17
source: dbSNP
start: 73390496
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390499
feature_type: variation
id: rs762969140
seq_region_name: 17
source: dbSNP
start: 73390499
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390500
feature_type: variation
id: rs113193365
seq_region_name: 17
source: dbSNP
start: 73390500
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390501
feature_type: variation
id: rs2062919125
seq_region_name: 17
source: dbSNP
start: 73390501
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390503
feature_type: variation
id: rs200029772
seq_region_name: 17
source: dbSNP
start: 73390503
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390505
feature_type: variation
id: rs775572460
seq_region_name: 17
source: dbSNP
start: 73390505
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390506
feature_type: variation
id: rs377296519
seq_region_name: 17
source: dbSNP
start: 73390506
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390507
feature_type: variation
id: rs1301367670
seq_region_name: 17
source: dbSNP
start: 73390507
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390509
feature_type: variation
id: rs1298723438
seq_region_name: 17
source: dbSNP
start: 73390509
strand: 1
-
alleles:
- GGCAAGCAAGGCAAGC
- GGCAAGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390525
feature_type: variation
id: rs2062919261
seq_region_name: 17
source: dbSNP
start: 73390510
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390513
feature_type: variation
id: rs931845066
seq_region_name: 17
source: dbSNP
start: 73390513
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390515
feature_type: variation
id: rs1363991474
seq_region_name: 17
source: dbSNP
start: 73390515
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390516
feature_type: variation
id: rs764328435
seq_region_name: 17
source: dbSNP
start: 73390516
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390521
feature_type: variation
id: rs754091938
seq_region_name: 17
source: dbSNP
start: 73390521
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390523
feature_type: variation
id: rs1312601321
seq_region_name: 17
source: dbSNP
start: 73390523
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390526
feature_type: variation
id: rs368453164
seq_region_name: 17
source: dbSNP
start: 73390526
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390527
feature_type: variation
id: rs765565675
seq_region_name: 17
source: dbSNP
start: 73390527
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390529
feature_type: variation
id: rs2145496464
seq_region_name: 17
source: dbSNP
start: 73390529
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390531
feature_type: variation
id: rs750847711
seq_region_name: 17
source: dbSNP
start: 73390531
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390536
feature_type: variation
id: rs536276635
seq_region_name: 17
source: dbSNP
start: 73390536
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390537
feature_type: variation
id: rs1168819142
seq_region_name: 17
source: dbSNP
start: 73390537
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390538
feature_type: variation
id: rs2062919545
seq_region_name: 17
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strand: 1
-
alleles:
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1215722647
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs769695977
seq_region_name: 17
source: dbSNP
start: 73390568
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs113806453
seq_region_name: 17
source: dbSNP
start: 73390571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390572
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062919865
seq_region_name: 17
source: dbSNP
start: 73390574
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1278017318
seq_region_name: 17
source: dbSNP
start: 73390577
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145496572
seq_region_name: 17
source: dbSNP
start: 73390579
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062919913
seq_region_name: 17
source: dbSNP
start: 73390580
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs954889128
seq_region_name: 17
source: dbSNP
start: 73390581
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1233465068
seq_region_name: 17
source: dbSNP
start: 73390582
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1348762087
seq_region_name: 17
source: dbSNP
start: 73390583
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062920000
seq_region_name: 17
source: dbSNP
start: 73390585
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1305688559
seq_region_name: 17
source: dbSNP
start: 73390589
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1319985726
seq_region_name: 17
source: dbSNP
start: 73390590
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs986542146
seq_region_name: 17
source: dbSNP
start: 73390595
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1015388550
seq_region_name: 17
source: dbSNP
start: 73390596
strand: 1
-
alleles:
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- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062920119
seq_region_name: 17
source: dbSNP
start: 73390596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062920141
seq_region_name: 17
source: dbSNP
start: 73390598
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062920164
seq_region_name: 17
source: dbSNP
start: 73390599
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1335353319
seq_region_name: 17
source: dbSNP
start: 73390601
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1329993259
seq_region_name: 17
source: dbSNP
start: 73390607
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390611
feature_type: variation
id: rs1568378635
seq_region_name: 17
source: dbSNP
start: 73390611
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390614
feature_type: variation
id: rs2062920311
seq_region_name: 17
source: dbSNP
start: 73390614
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1393437482
seq_region_name: 17
source: dbSNP
start: 73390615
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1374025768
seq_region_name: 17
source: dbSNP
start: 73390621
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390623
feature_type: variation
id: rs562775005
seq_region_name: 17
source: dbSNP
start: 73390623
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062920358
seq_region_name: 17
source: dbSNP
start: 73390625
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390628
feature_type: variation
id: rs961029953
seq_region_name: 17
source: dbSNP
start: 73390628
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390630
feature_type: variation
id: rs1312868346
seq_region_name: 17
source: dbSNP
start: 73390630
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390632
feature_type: variation
id: rs532965204
seq_region_name: 17
source: dbSNP
start: 73390632
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568378645
seq_region_name: 17
source: dbSNP
start: 73390634
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390637
feature_type: variation
id: rs2145496701
seq_region_name: 17
source: dbSNP
start: 73390637
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390640
feature_type: variation
id: rs1599515304
seq_region_name: 17
source: dbSNP
start: 73390640
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390643
feature_type: variation
id: rs1439997390
seq_region_name: 17
source: dbSNP
start: 73390643
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390644
feature_type: variation
id: rs1599515317
seq_region_name: 17
source: dbSNP
start: 73390644
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390650
feature_type: variation
id: rs1395201286
seq_region_name: 17
source: dbSNP
start: 73390650
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390659
feature_type: variation
id: rs2062920573
seq_region_name: 17
source: dbSNP
start: 73390659
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390660
feature_type: variation
id: rs544764774
seq_region_name: 17
source: dbSNP
start: 73390660
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390662
feature_type: variation
id: rs559855897
seq_region_name: 17
source: dbSNP
start: 73390662
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390668
feature_type: variation
id: rs2062920655
seq_region_name: 17
source: dbSNP
start: 73390668
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390672
feature_type: variation
id: rs1362801666
seq_region_name: 17
source: dbSNP
start: 73390672
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390673
feature_type: variation
id: rs1599515333
seq_region_name: 17
source: dbSNP
start: 73390673
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390674
feature_type: variation
id: rs2062920721
seq_region_name: 17
source: dbSNP
start: 73390674
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390678
feature_type: variation
id: rs2062920740
seq_region_name: 17
source: dbSNP
start: 73390678
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390678
feature_type: variation
id: rs2062920768
seq_region_name: 17
source: dbSNP
start: 73390678
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390679
feature_type: variation
id: rs2062920798
seq_region_name: 17
source: dbSNP
start: 73390679
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390688
feature_type: variation
id: rs2062920818
seq_region_name: 17
source: dbSNP
start: 73390688
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390689
feature_type: variation
id: rs1418264119
seq_region_name: 17
source: dbSNP
start: 73390689
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390695
feature_type: variation
id: rs2062920859
seq_region_name: 17
source: dbSNP
start: 73390695
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390696
feature_type: variation
id: rs2062920879
seq_region_name: 17
source: dbSNP
start: 73390695
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390700
feature_type: variation
id: rs1473488638
seq_region_name: 17
source: dbSNP
start: 73390700
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390702
feature_type: variation
id: rs2062920927
seq_region_name: 17
source: dbSNP
start: 73390702
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390706
feature_type: variation
id: rs1599515340
seq_region_name: 17
source: dbSNP
start: 73390706
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390708
feature_type: variation
id: rs778282905
seq_region_name: 17
source: dbSNP
start: 73390708
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390710
feature_type: variation
id: rs2062921006
seq_region_name: 17
source: dbSNP
start: 73390710
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390711
feature_type: variation
id: rs1048660174
seq_region_name: 17
source: dbSNP
start: 73390711
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390712
feature_type: variation
id: rs906122430
seq_region_name: 17
source: dbSNP
start: 73390712
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390713
feature_type: variation
id: rs919824608
seq_region_name: 17
source: dbSNP
start: 73390713
strand: 1
-
alleles:
- TCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390715
feature_type: variation
id: rs1210137142
seq_region_name: 17
source: dbSNP
start: 73390713
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390718
feature_type: variation
id: rs1566296
seq_region_name: 17
source: dbSNP
start: 73390718
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390720
feature_type: variation
id: rs1280862582
seq_region_name: 17
source: dbSNP
start: 73390720
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390721
feature_type: variation
id: rs2062921160
seq_region_name: 17
source: dbSNP
start: 73390721
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390724
feature_type: variation
id: rs1203411897
seq_region_name: 17
source: dbSNP
start: 73390724
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390725
feature_type: variation
id: rs548997757
seq_region_name: 17
source: dbSNP
start: 73390725
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390727
feature_type: variation
id: rs2062921234
seq_region_name: 17
source: dbSNP
start: 73390727
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390731
feature_type: variation
id: rs2062921251
seq_region_name: 17
source: dbSNP
start: 73390731
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390732
feature_type: variation
id: rs895949391
seq_region_name: 17
source: dbSNP
start: 73390732
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390734
feature_type: variation
id: rs1568378686
seq_region_name: 17
source: dbSNP
start: 73390734
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390743
feature_type: variation
id: rs1241440245
seq_region_name: 17
source: dbSNP
start: 73390743
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390748
feature_type: variation
id: rs2062921336
seq_region_name: 17
source: dbSNP
start: 73390748
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390750
feature_type: variation
id: rs980011090
seq_region_name: 17
source: dbSNP
start: 73390750
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390752
feature_type: variation
id: rs1354012584
seq_region_name: 17
source: dbSNP
start: 73390752
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390753
feature_type: variation
id: rs2062921397
seq_region_name: 17
source: dbSNP
start: 73390753
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390755
feature_type: variation
id: rs749100926
seq_region_name: 17
source: dbSNP
start: 73390755
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390757
feature_type: variation
id: rs1332349321
seq_region_name: 17
source: dbSNP
start: 73390757
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390768
feature_type: variation
id: rs1599515416
seq_region_name: 17
source: dbSNP
start: 73390768
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- GG
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assembly_name: GRCh38
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73390888
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390895
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73390898
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73390900
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73390901
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73390908
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73390919
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390920
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390923
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390924
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73390926
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390927
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73390928
strand: 1
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alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390929
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73390930
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390933
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390934
strand: 1
-
alleles:
- CCCCC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390938
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390934
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145497321
seq_region_name: 17
source: dbSNP
start: 73390936
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390938
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs961430840
seq_region_name: 17
source: dbSNP
start: 73390939
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390940
feature_type: variation
id: rs1368336734
seq_region_name: 17
source: dbSNP
start: 73390940
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390943
feature_type: variation
id: rs1568378790
seq_region_name: 17
source: dbSNP
start: 73390943
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs551998958
seq_region_name: 17
source: dbSNP
start: 73390949
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390954
feature_type: variation
id: rs2062923318
seq_region_name: 17
source: dbSNP
start: 73390954
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390961
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs567001410
seq_region_name: 17
source: dbSNP
start: 73390962
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390963
feature_type: variation
id: rs142707878
seq_region_name: 17
source: dbSNP
start: 73390963
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390964
feature_type: variation
id: rs545218502
seq_region_name: 17
source: dbSNP
start: 73390964
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs866792958
seq_region_name: 17
source: dbSNP
start: 73390965
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390970
feature_type: variation
id: rs1420071459
seq_region_name: 17
source: dbSNP
start: 73390970
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390971
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73390971
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73390978
feature_type: variation
id: rs1452732010
seq_region_name: 17
source: dbSNP
start: 73390972
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73391040
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73391044
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73391053
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73391068
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391071
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391082
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73391085
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391088
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391090
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391092
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391104
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391109
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391113
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391120
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391121
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs899353198
seq_region_name: 17
source: dbSNP
start: 73391122
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73391124
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391124
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062924799
seq_region_name: 17
source: dbSNP
start: 73391126
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1461730521
seq_region_name: 17
source: dbSNP
start: 73391135
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599515821
seq_region_name: 17
source: dbSNP
start: 73391137
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391138
feature_type: variation
id: rs1222839442
seq_region_name: 17
source: dbSNP
start: 73391138
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs559898649
seq_region_name: 17
source: dbSNP
start: 73391139
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391140
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391142
feature_type: variation
id: rs2145497813
seq_region_name: 17
source: dbSNP
start: 73391142
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1289946391
seq_region_name: 17
source: dbSNP
start: 73391145
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062924962
seq_region_name: 17
source: dbSNP
start: 73391146
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1412890092
seq_region_name: 17
source: dbSNP
start: 73391149
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568378866
seq_region_name: 17
source: dbSNP
start: 73391151
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs754360951
seq_region_name: 17
source: dbSNP
start: 73391152
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391153
feature_type: variation
id: rs560446772
seq_region_name: 17
source: dbSNP
start: 73391153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391156
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391157
feature_type: variation
id: rs917488624
seq_region_name: 17
source: dbSNP
start: 73391157
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs572156341
seq_region_name: 17
source: dbSNP
start: 73391160
strand: 1
-
alleles:
- TTACCAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391168
feature_type: variation
id: rs1457941032
seq_region_name: 17
source: dbSNP
start: 73391162
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs946282896
seq_region_name: 17
source: dbSNP
start: 73391165
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391171
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391174
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1384880537
seq_region_name: 17
source: dbSNP
start: 73391175
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1258749825
seq_region_name: 17
source: dbSNP
start: 73391177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391180
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391184
feature_type: variation
id: rs1035543464
seq_region_name: 17
source: dbSNP
start: 73391184
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391185
feature_type: variation
id: rs1955622576
seq_region_name: 17
source: dbSNP
start: 73391185
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391187
feature_type: variation
id: rs572172108
seq_region_name: 17
source: dbSNP
start: 73391187
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391190
feature_type: variation
id: rs541285313
seq_region_name: 17
source: dbSNP
start: 73391190
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391192
feature_type: variation
id: rs2062925326
seq_region_name: 17
source: dbSNP
start: 73391192
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391197
feature_type: variation
id: rs1341114524
seq_region_name: 17
source: dbSNP
start: 73391197
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391199
feature_type: variation
id: rs1329372957
seq_region_name: 17
source: dbSNP
start: 73391199
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391201
feature_type: variation
id: rs988769439
seq_region_name: 17
source: dbSNP
start: 73391201
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391206
feature_type: variation
id: rs542378588
seq_region_name: 17
source: dbSNP
start: 73391206
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391207
feature_type: variation
id: rs868330132
seq_region_name: 17
source: dbSNP
start: 73391207
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391208
feature_type: variation
id: rs1313430648
seq_region_name: 17
source: dbSNP
start: 73391208
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391210
feature_type: variation
id: rs2062925528
seq_region_name: 17
source: dbSNP
start: 73391210
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391211
feature_type: variation
id: rs2062925550
seq_region_name: 17
source: dbSNP
start: 73391211
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391215
feature_type: variation
id: rs560989904
seq_region_name: 17
source: dbSNP
start: 73391215
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391216
feature_type: variation
id: rs1360008463
seq_region_name: 17
source: dbSNP
start: 73391216
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391220
feature_type: variation
id: rs542051664
seq_region_name: 17
source: dbSNP
start: 73391220
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391221
feature_type: variation
id: rs1288324953
seq_region_name: 17
source: dbSNP
start: 73391221
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391230
feature_type: variation
id: rs2145498016
seq_region_name: 17
source: dbSNP
start: 73391230
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391240
feature_type: variation
id: rs2062925669
seq_region_name: 17
source: dbSNP
start: 73391240
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391242
feature_type: variation
id: rs2062925688
seq_region_name: 17
source: dbSNP
start: 73391242
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391247
feature_type: variation
id: rs2062925718
seq_region_name: 17
source: dbSNP
start: 73391247
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391252
feature_type: variation
id: rs2062925735
seq_region_name: 17
source: dbSNP
start: 73391252
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391254
feature_type: variation
id: rs149496335
seq_region_name: 17
source: dbSNP
start: 73391254
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391256
feature_type: variation
id: rs563219691
seq_region_name: 17
source: dbSNP
start: 73391256
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391257
feature_type: variation
id: rs533647951
seq_region_name: 17
source: dbSNP
start: 73391257
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391258
feature_type: variation
id: rs552039887
seq_region_name: 17
source: dbSNP
start: 73391258
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391262
feature_type: variation
id: rs567088802
seq_region_name: 17
source: dbSNP
start: 73391262
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391267
feature_type: variation
id: rs765525773
seq_region_name: 17
source: dbSNP
start: 73391267
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391268
feature_type: variation
id: rs1427226936
seq_region_name: 17
source: dbSNP
start: 73391268
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391269
feature_type: variation
id: rs1259091375
seq_region_name: 17
source: dbSNP
start: 73391269
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391273
feature_type: variation
id: rs2062925997
seq_region_name: 17
source: dbSNP
start: 73391273
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391274
feature_type: variation
id: rs375550380
seq_region_name: 17
source: dbSNP
start: 73391274
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391287
feature_type: variation
id: rs1036644126
seq_region_name: 17
source: dbSNP
start: 73391287
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391293
feature_type: variation
id: rs2145498125
seq_region_name: 17
source: dbSNP
start: 73391293
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391296
feature_type: variation
id: rs899320686
seq_region_name: 17
source: dbSNP
start: 73391296
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391298
feature_type: variation
id: rs2062926114
seq_region_name: 17
source: dbSNP
start: 73391297
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391301
feature_type: variation
id: rs2145498142
seq_region_name: 17
source: dbSNP
start: 73391301
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391304
feature_type: variation
id: rs2062926146
seq_region_name: 17
source: dbSNP
start: 73391304
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391311
feature_type: variation
id: rs2062926170
seq_region_name: 17
source: dbSNP
start: 73391311
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391312
feature_type: variation
id: rs2062926205
seq_region_name: 17
source: dbSNP
start: 73391312
strand: 1
-
alleles:
- CATTCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391317
feature_type: variation
id: rs1249428043
seq_region_name: 17
source: dbSNP
start: 73391312
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391315
feature_type: variation
id: rs930866334
seq_region_name: 17
source: dbSNP
start: 73391315
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391322
feature_type: variation
id: rs1211428129
seq_region_name: 17
source: dbSNP
start: 73391322
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391324
feature_type: variation
id: rs1333965471
seq_region_name: 17
source: dbSNP
start: 73391324
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391327
feature_type: variation
id: rs2062926303
seq_region_name: 17
source: dbSNP
start: 73391327
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391328
feature_type: variation
id: rs1265786037
seq_region_name: 17
source: dbSNP
start: 73391328
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391330
feature_type: variation
id: rs2062926351
seq_region_name: 17
source: dbSNP
start: 73391330
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391332
feature_type: variation
id: rs2062926368
seq_region_name: 17
source: dbSNP
start: 73391332
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391338
feature_type: variation
id: rs2062926396
seq_region_name: 17
source: dbSNP
start: 73391338
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391339
feature_type: variation
id: rs1246946211
seq_region_name: 17
source: dbSNP
start: 73391339
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391341
feature_type: variation
id: rs1305648370
seq_region_name: 17
source: dbSNP
start: 73391340
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391342
feature_type: variation
id: rs2062926424
seq_region_name: 17
source: dbSNP
start: 73391342
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391355
feature_type: variation
id: rs2145498236
seq_region_name: 17
source: dbSNP
start: 73391355
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391356
feature_type: variation
id: rs549214375
seq_region_name: 17
source: dbSNP
start: 73391356
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391359
feature_type: variation
id: rs1488936229
seq_region_name: 17
source: dbSNP
start: 73391359
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391360
feature_type: variation
id: rs1294967057
seq_region_name: 17
source: dbSNP
start: 73391360
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391366
feature_type: variation
id: rs1568378951
seq_region_name: 17
source: dbSNP
start: 73391366
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391367
feature_type: variation
id: rs1229148498
seq_region_name: 17
source: dbSNP
start: 73391367
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391372
feature_type: variation
id: rs2062926557
seq_region_name: 17
source: dbSNP
start: 73391372
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391374
feature_type: variation
id: rs1195926635
seq_region_name: 17
source: dbSNP
start: 73391374
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391376
feature_type: variation
id: rs1048585280
seq_region_name: 17
source: dbSNP
start: 73391376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391378
feature_type: variation
id: rs1599516037
seq_region_name: 17
source: dbSNP
start: 73391378
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391382
feature_type: variation
id: rs2062926657
seq_region_name: 17
source: dbSNP
start: 73391382
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391383
feature_type: variation
id: rs2062926678
seq_region_name: 17
source: dbSNP
start: 73391383
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391386
feature_type: variation
id: rs1261034032
seq_region_name: 17
source: dbSNP
start: 73391386
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391389
feature_type: variation
id: rs2062926728
seq_region_name: 17
source: dbSNP
start: 73391389
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391390
feature_type: variation
id: rs1324207273
seq_region_name: 17
source: dbSNP
start: 73391390
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391391
feature_type: variation
id: rs758943333
seq_region_name: 17
source: dbSNP
start: 73391391
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391392
feature_type: variation
id: rs780433227
seq_region_name: 17
source: dbSNP
start: 73391392
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391393
feature_type: variation
id: rs746475465
seq_region_name: 17
source: dbSNP
start: 73391393
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391395
feature_type: variation
id: rs754475055
seq_region_name: 17
source: dbSNP
start: 73391395
strand: 1
-
alleles:
- CTTCCTTC
- CTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391402
feature_type: variation
id: rs758800827
seq_region_name: 17
source: dbSNP
start: 73391395
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391399
feature_type: variation
id: rs773505322
seq_region_name: 17
source: dbSNP
start: 73391399
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391400
feature_type: variation
id: rs1372949854
seq_region_name: 17
source: dbSNP
start: 73391400
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391402
feature_type: variation
id: rs1235824840
seq_region_name: 17
source: dbSNP
start: 73391402
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391406
feature_type: variation
id: rs1167417071
seq_region_name: 17
source: dbSNP
start: 73391406
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391413
feature_type: variation
id: rs747778580
seq_region_name: 17
source: dbSNP
start: 73391413
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391414
feature_type: variation
id: rs769627250
seq_region_name: 17
source: dbSNP
start: 73391414
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391415
feature_type: variation
id: rs7214272
seq_region_name: 17
source: dbSNP
start: 73391415
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391417
feature_type: variation
id: rs2062927092
seq_region_name: 17
source: dbSNP
start: 73391417
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391420
feature_type: variation
id: rs376324123
seq_region_name: 17
source: dbSNP
start: 73391420
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391421
feature_type: variation
id: rs758640275
seq_region_name: 17
source: dbSNP
start: 73391421
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391422
feature_type: variation
id: rs1568378984
seq_region_name: 17
source: dbSNP
start: 73391422
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391423
feature_type: variation
id: rs1211357315
seq_region_name: 17
source: dbSNP
start: 73391423
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391426
feature_type: variation
id: rs1428520442
seq_region_name: 17
source: dbSNP
start: 73391426
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73391432
feature_type: variation
id: rs2062927243
seq_region_name: 17
source: dbSNP
start: 73391432
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73391434
feature_type: variation
id: rs2062927263
seq_region_name: 17
source: dbSNP
start: 73391434
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391449
feature_type: variation
id: rs1252710388
seq_region_name: 17
source: dbSNP
start: 73391449
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391450
feature_type: variation
id: rs537894049
seq_region_name: 17
source: dbSNP
start: 73391450
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73391454
feature_type: variation
id: rs540415385
seq_region_name: 17
source: dbSNP
start: 73391454
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391458
feature_type: variation
id: rs1368028526
seq_region_name: 17
source: dbSNP
start: 73391458
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391461
feature_type: variation
id: rs201339333
seq_region_name: 17
source: dbSNP
start: 73391461
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391462
feature_type: variation
id: rs577548698
seq_region_name: 17
source: dbSNP
start: 73391462
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391464
feature_type: variation
id: rs762012928
seq_region_name: 17
source: dbSNP
start: 73391464
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391465
feature_type: variation
id: rs953459109
seq_region_name: 17
source: dbSNP
start: 73391465
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391468
feature_type: variation
id: rs2062927520
seq_region_name: 17
source: dbSNP
start: 73391468
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391470
feature_type: variation
id: rs1301302041
seq_region_name: 17
source: dbSNP
start: 73391470
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391477
feature_type: variation
id: rs1233882064
seq_region_name: 17
source: dbSNP
start: 73391477
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391478
feature_type: variation
id: rs1331847990
seq_region_name: 17
source: dbSNP
start: 73391478
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391480
feature_type: variation
id: rs987576224
seq_region_name: 17
source: dbSNP
start: 73391480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391484
feature_type: variation
id: rs200895362
seq_region_name: 17
source: dbSNP
start: 73391484
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391485
feature_type: variation
id: rs750724769
seq_region_name: 17
source: dbSNP
start: 73391485
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391488
feature_type: variation
id: rs143947190
seq_region_name: 17
source: dbSNP
start: 73391488
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391490
feature_type: variation
id: rs1599516244
seq_region_name: 17
source: dbSNP
start: 73391490
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391492
feature_type: variation
id: rs751976433
seq_region_name: 17
source: dbSNP
start: 73391492
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73391493
feature_type: variation
id: rs35289088
seq_region_name: 17
source: dbSNP
start: 73391493
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391498
feature_type: variation
id: rs2062927848
seq_region_name: 17
source: dbSNP
start: 73391498
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391499
feature_type: variation
id: rs199888450
seq_region_name: 17
source: dbSNP
start: 73391499
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391500
feature_type: variation
id: rs1195895525
seq_region_name: 17
source: dbSNP
start: 73391500
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391504
feature_type: variation
id: rs2062927929
seq_region_name: 17
source: dbSNP
start: 73391504
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391510
feature_type: variation
id: rs752321254
seq_region_name: 17
source: dbSNP
start: 73391510
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391513
feature_type: variation
id: rs2062927988
seq_region_name: 17
source: dbSNP
start: 73391513
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391515
feature_type: variation
id: rs1454025745
seq_region_name: 17
source: dbSNP
start: 73391515
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391518
feature_type: variation
id: rs755760410
seq_region_name: 17
source: dbSNP
start: 73391518
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73391519
feature_type: variation
id: rs977680878
seq_region_name: 17
source: dbSNP
start: 73391519
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391520
feature_type: variation
id: rs777581995
seq_region_name: 17
source: dbSNP
start: 73391520
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391521
feature_type: variation
id: rs1399092587
seq_region_name: 17
source: dbSNP
start: 73391521
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73391523
feature_type: variation
id: rs1377779329
seq_region_name: 17
source: dbSNP
start: 73391523
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391530
feature_type: variation
id: rs1200548333
seq_region_name: 17
source: dbSNP
start: 73391530
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73391535
feature_type: variation
id: rs2062928220
seq_region_name: 17
source: dbSNP
start: 73391535
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: splice_region_variant
end: 73391542
feature_type: variation
id: rs749063119
seq_region_name: 17
source: dbSNP
start: 73391542
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73391543
feature_type: variation
id: rs2062928274
seq_region_name: 17
source: dbSNP
start: 73391543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73391544
feature_type: variation
id: rs770664507
seq_region_name: 17
source: dbSNP
start: 73391544
strand: 1
-
alleles:
- GGGGG
- GGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73391548
feature_type: variation
id: rs780216130
seq_region_name: 17
source: dbSNP
start: 73391544
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73391545
feature_type: variation
id: rs778810828
seq_region_name: 17
source: dbSNP
start: 73391545
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73391546
feature_type: variation
id: rs745772093
seq_region_name: 17
source: dbSNP
start: 73391546
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73391547
feature_type: variation
id: rs2062928397
seq_region_name: 17
source: dbSNP
start: 73391547
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73391548
feature_type: variation
id: rs2062928415
seq_region_name: 17
source: dbSNP
start: 73391548
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391558
feature_type: variation
id: rs1483971217
seq_region_name: 17
source: dbSNP
start: 73391558
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391561
feature_type: variation
id: rs2145498813
seq_region_name: 17
source: dbSNP
start: 73391561
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391562
feature_type: variation
id: rs572150091
seq_region_name: 17
source: dbSNP
start: 73391562
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391563
feature_type: variation
id: rs542764573
seq_region_name: 17
source: dbSNP
start: 73391563
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391564
feature_type: variation
id: rs373481242
seq_region_name: 17
source: dbSNP
start: 73391564
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391565
feature_type: variation
id: rs773333254
seq_region_name: 17
source: dbSNP
start: 73391565
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391566
feature_type: variation
id: rs763272669
seq_region_name: 17
source: dbSNP
start: 73391566
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391567
feature_type: variation
id: rs2062928637
seq_region_name: 17
source: dbSNP
start: 73391567
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391574
feature_type: variation
id: rs2062928661
seq_region_name: 17
source: dbSNP
start: 73391574
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391576
feature_type: variation
id: rs2145498861
seq_region_name: 17
source: dbSNP
start: 73391576
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391579
feature_type: variation
id: rs1336122297
seq_region_name: 17
source: dbSNP
start: 73391579
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391580
feature_type: variation
id: rs930777855
seq_region_name: 17
source: dbSNP
start: 73391580
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391581
feature_type: variation
id: rs766628229
seq_region_name: 17
source: dbSNP
start: 73391581
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391584
feature_type: variation
id: rs1375035183
seq_region_name: 17
source: dbSNP
start: 73391584
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391588
feature_type: variation
id: rs2062928769
seq_region_name: 17
source: dbSNP
start: 73391588
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391589
feature_type: variation
id: rs1412252767
seq_region_name: 17
source: dbSNP
start: 73391589
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391592
feature_type: variation
id: rs889203153
seq_region_name: 17
source: dbSNP
start: 73391592
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391594
feature_type: variation
id: rs73999031
seq_region_name: 17
source: dbSNP
start: 73391594
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391595
feature_type: variation
id: rs1413482148
seq_region_name: 17
source: dbSNP
start: 73391595
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391597
feature_type: variation
id: rs1402279631
seq_region_name: 17
source: dbSNP
start: 73391597
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391601
feature_type: variation
id: rs2062928926
seq_region_name: 17
source: dbSNP
start: 73391601
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391605
feature_type: variation
id: rs576082510
seq_region_name: 17
source: dbSNP
start: 73391605
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391606
feature_type: variation
id: rs1485559929
seq_region_name: 17
source: dbSNP
start: 73391606
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391609
feature_type: variation
id: rs1473538902
seq_region_name: 17
source: dbSNP
start: 73391609
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391611
feature_type: variation
id: rs2145498965
seq_region_name: 17
source: dbSNP
start: 73391611
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391613
feature_type: variation
id: rs2062929051
seq_region_name: 17
source: dbSNP
start: 73391613
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391617
feature_type: variation
id: rs117971083
seq_region_name: 17
source: dbSNP
start: 73391617
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391619
feature_type: variation
id: rs2062929093
seq_region_name: 17
source: dbSNP
start: 73391619
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391621
feature_type: variation
id: rs1056845696
seq_region_name: 17
source: dbSNP
start: 73391621
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391622
feature_type: variation
id: rs1186744211
seq_region_name: 17
source: dbSNP
start: 73391622
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391623
feature_type: variation
id: rs1599516422
seq_region_name: 17
source: dbSNP
start: 73391623
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391624
feature_type: variation
id: rs1443131853
seq_region_name: 17
source: dbSNP
start: 73391624
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391625
feature_type: variation
id: rs564860843
seq_region_name: 17
source: dbSNP
start: 73391625
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391627
feature_type: variation
id: rs1599516441
seq_region_name: 17
source: dbSNP
start: 73391627
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391631
feature_type: variation
id: rs1009905639
seq_region_name: 17
source: dbSNP
start: 73391631
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391632
feature_type: variation
id: rs2062929264
seq_region_name: 17
source: dbSNP
start: 73391632
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391633
feature_type: variation
id: rs1328700465
seq_region_name: 17
source: dbSNP
start: 73391633
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391639
feature_type: variation
id: rs532112508
seq_region_name: 17
source: dbSNP
start: 73391639
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391641
feature_type: variation
id: rs2062929351
seq_region_name: 17
source: dbSNP
start: 73391641
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391643
feature_type: variation
id: rs887644675
seq_region_name: 17
source: dbSNP
start: 73391643
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391644
feature_type: variation
id: rs1293280986
seq_region_name: 17
source: dbSNP
start: 73391644
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391645
feature_type: variation
id: rs1380621497
seq_region_name: 17
source: dbSNP
start: 73391645
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391647
feature_type: variation
id: rs545740453
seq_region_name: 17
source: dbSNP
start: 73391647
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391650
feature_type: variation
id: rs1001988051
seq_region_name: 17
source: dbSNP
start: 73391650
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391654
feature_type: variation
id: rs375356629
seq_region_name: 17
source: dbSNP
start: 73391654
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391659
feature_type: variation
id: rs1380190706
seq_region_name: 17
source: dbSNP
start: 73391659
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391664
feature_type: variation
id: rs960742458
seq_region_name: 17
source: dbSNP
start: 73391664
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73391673
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73391890
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73391896
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73391899
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73391901
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73391903
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73391905
strand: 1
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assembly_name: GRCh38
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source: dbSNP
start: 73391907
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73391910
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73391914
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391915
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73391916
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73391917
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1019005634
seq_region_name: 17
source: dbSNP
start: 73391918
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1277550914
seq_region_name: 17
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-
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392012
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73392026
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73392035
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392045
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392048
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392050
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392051
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392053
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392054
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392055
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392061
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392063
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392065
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73392066
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392067
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73392069
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73392074
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392083
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392084
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73392085
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392088
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145500046
seq_region_name: 17
source: dbSNP
start: 73392103
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392105
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392110
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392111
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73392119
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs376152913
seq_region_name: 17
source: dbSNP
start: 73392141
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392143
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id: rs1479804022
seq_region_name: 17
source: dbSNP
start: 73392143
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392144
feature_type: variation
id: rs1041888712
seq_region_name: 17
source: dbSNP
start: 73392144
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392149
feature_type: variation
id: rs1423702736
seq_region_name: 17
source: dbSNP
start: 73392149
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392151
feature_type: variation
id: rs1599517042
seq_region_name: 17
source: dbSNP
start: 73392151
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392152
feature_type: variation
id: rs1170828893
seq_region_name: 17
source: dbSNP
start: 73392152
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392153
feature_type: variation
id: rs1181881760
seq_region_name: 17
source: dbSNP
start: 73392153
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392157
feature_type: variation
id: rs1484033719
seq_region_name: 17
source: dbSNP
start: 73392157
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392158
feature_type: variation
id: rs778598095
seq_region_name: 17
source: dbSNP
start: 73392158
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392165
feature_type: variation
id: rs1568379266
seq_region_name: 17
source: dbSNP
start: 73392165
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392168
feature_type: variation
id: rs2062933434
seq_region_name: 17
source: dbSNP
start: 73392168
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392170
feature_type: variation
id: rs1599517065
seq_region_name: 17
source: dbSNP
start: 73392170
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392174
feature_type: variation
id: rs1425325967
seq_region_name: 17
source: dbSNP
start: 73392174
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs2062933537
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strand: 1
-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392207
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73392214
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73392218
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73392220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392221
strand: 1
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alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392223
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392242
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392248
strand: 1
-
alleles:
- "-"
- GAC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392253
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392259
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392264
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392272
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392272
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392273
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392273
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392274
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1428342934
seq_region_name: 17
source: dbSNP
start: 73392275
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392277
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392279
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1368194317
seq_region_name: 17
source: dbSNP
start: 73392281
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392287
feature_type: variation
id: rs1378288470
seq_region_name: 17
source: dbSNP
start: 73392287
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392289
feature_type: variation
id: rs1430017571
seq_region_name: 17
source: dbSNP
start: 73392288
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392289
feature_type: variation
id: rs1490181799
seq_region_name: 17
source: dbSNP
start: 73392289
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1196299261
seq_region_name: 17
source: dbSNP
start: 73392293
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1042571691
seq_region_name: 17
source: dbSNP
start: 73392294
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392298
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392300
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392301
feature_type: variation
id: rs1264641117
seq_region_name: 17
source: dbSNP
start: 73392301
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062934890
seq_region_name: 17
source: dbSNP
start: 73392302
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392304
feature_type: variation
id: rs2062934908
seq_region_name: 17
source: dbSNP
start: 73392304
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392305
feature_type: variation
id: rs532516372
seq_region_name: 17
source: dbSNP
start: 73392305
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392306
feature_type: variation
id: rs1476569026
seq_region_name: 17
source: dbSNP
start: 73392306
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392315
feature_type: variation
id: rs1274035233
seq_region_name: 17
source: dbSNP
start: 73392315
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392320
feature_type: variation
id: rs1599517298
seq_region_name: 17
source: dbSNP
start: 73392320
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392321
feature_type: variation
id: rs2062935032
seq_region_name: 17
source: dbSNP
start: 73392321
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392322
feature_type: variation
id: rs1599517303
seq_region_name: 17
source: dbSNP
start: 73392322
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392325
feature_type: variation
id: rs897681388
seq_region_name: 17
source: dbSNP
start: 73392325
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392326
feature_type: variation
id: rs1032025083
seq_region_name: 17
source: dbSNP
start: 73392326
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392329
feature_type: variation
id: rs1254549255
seq_region_name: 17
source: dbSNP
start: 73392329
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392330
feature_type: variation
id: rs1232773907
seq_region_name: 17
source: dbSNP
start: 73392330
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392331
feature_type: variation
id: rs993587531
seq_region_name: 17
source: dbSNP
start: 73392331
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392333
feature_type: variation
id: rs2145500641
seq_region_name: 17
source: dbSNP
start: 73392333
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392344
feature_type: variation
id: rs1599517329
seq_region_name: 17
source: dbSNP
start: 73392344
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392348
feature_type: variation
id: rs2145500651
seq_region_name: 17
source: dbSNP
start: 73392348
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392352
feature_type: variation
id: rs35515835
seq_region_name: 17
source: dbSNP
start: 73392352
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392355
feature_type: variation
id: rs1303805431
seq_region_name: 17
source: dbSNP
start: 73392355
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392356
feature_type: variation
id: rs188803421
seq_region_name: 17
source: dbSNP
start: 73392356
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392357
feature_type: variation
id: rs1350343354
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392480
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73392481
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392483
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392484
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392485
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392488
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392491
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392493
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392500
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392502
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs910243022
seq_region_name: 17
source: dbSNP
start: 73392503
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392504
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73392506
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1040727483
seq_region_name: 17
source: dbSNP
start: 73392507
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062936602
seq_region_name: 17
source: dbSNP
start: 73392508
strand: 1
-
alleles:
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- CTGCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2040289026
seq_region_name: 17
source: dbSNP
start: 73392510
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392512
strand: 1
-
alleles:
- CC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs34503077
seq_region_name: 17
source: dbSNP
start: 73392526
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs57261530
seq_region_name: 17
source: dbSNP
start: 73392529
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062936704
seq_region_name: 17
source: dbSNP
start: 73392531
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392542
feature_type: variation
id: rs1568379422
seq_region_name: 17
source: dbSNP
start: 73392542
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392544
feature_type: variation
id: rs368765111
seq_region_name: 17
source: dbSNP
start: 73392544
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392546
feature_type: variation
id: rs1398998323
seq_region_name: 17
source: dbSNP
start: 73392546
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1317790857
seq_region_name: 17
source: dbSNP
start: 73392548
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392549
feature_type: variation
id: rs1359957520
seq_region_name: 17
source: dbSNP
start: 73392549
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392550
feature_type: variation
id: rs1387670576
seq_region_name: 17
source: dbSNP
start: 73392550
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392557
feature_type: variation
id: rs1049108732
seq_region_name: 17
source: dbSNP
start: 73392557
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392558
feature_type: variation
id: rs887873634
seq_region_name: 17
source: dbSNP
start: 73392558
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392560
feature_type: variation
id: rs1402384877
seq_region_name: 17
source: dbSNP
start: 73392560
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392561
feature_type: variation
id: rs1002135013
seq_region_name: 17
source: dbSNP
start: 73392561
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392563
feature_type: variation
id: rs1162583260
seq_region_name: 17
source: dbSNP
start: 73392563
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392567
feature_type: variation
id: rs1450402463
seq_region_name: 17
source: dbSNP
start: 73392567
strand: 1
-
alleles:
- AAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392581
feature_type: variation
id: rs1313224251
seq_region_name: 17
source: dbSNP
start: 73392579
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392592
feature_type: variation
id: rs2062937022
seq_region_name: 17
source: dbSNP
start: 73392592
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392595
feature_type: variation
id: rs2062937041
seq_region_name: 17
source: dbSNP
start: 73392595
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73392601
feature_type: variation
id: rs902099624
seq_region_name: 17
source: dbSNP
start: 73392601
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73392783
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392787
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73392794
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392817
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73392823
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392824
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73392827
strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1048008473
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1006397158
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1346625991
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1429976872
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393206
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393214
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393217
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393219
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393222
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599518239
seq_region_name: 17
source: dbSNP
start: 73393223
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1254637303
seq_region_name: 17
source: dbSNP
start: 73393227
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062942409
seq_region_name: 17
source: dbSNP
start: 73393229
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062942429
seq_region_name: 17
source: dbSNP
start: 73393230
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599518249
seq_region_name: 17
source: dbSNP
start: 73393231
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393232
feature_type: variation
id: rs2145502603
seq_region_name: 17
source: dbSNP
start: 73393232
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062942475
seq_region_name: 17
source: dbSNP
start: 73393234
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062942498
seq_region_name: 17
source: dbSNP
start: 73393236
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1233061204
seq_region_name: 17
source: dbSNP
start: 73393238
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599518259
seq_region_name: 17
source: dbSNP
start: 73393239
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393240
feature_type: variation
id: rs2062942561
seq_region_name: 17
source: dbSNP
start: 73393240
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1383515113
seq_region_name: 17
source: dbSNP
start: 73393241
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062942608
seq_region_name: 17
source: dbSNP
start: 73393241
strand: 1
-
alleles:
- TC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393242
feature_type: variation
id: rs2145502649
seq_region_name: 17
source: dbSNP
start: 73393241
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393241
feature_type: variation
id: rs2062942623
seq_region_name: 17
source: dbSNP
start: 73393242
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393242
feature_type: variation
id: rs1389020213
seq_region_name: 17
source: dbSNP
start: 73393242
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062942672
seq_region_name: 17
source: dbSNP
start: 73393242
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062942699
seq_region_name: 17
source: dbSNP
start: 73393242
strand: 1
-
alleles:
- "-"
- CA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393242
feature_type: variation
id: rs2062942735
seq_region_name: 17
source: dbSNP
start: 73393243
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393243
feature_type: variation
id: rs1422594637
seq_region_name: 17
source: dbSNP
start: 73393243
strand: 1
-
alleles:
- AAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393264
feature_type: variation
id: rs11443969
seq_region_name: 17
source: dbSNP
start: 73393243
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393244
feature_type: variation
id: rs1599518292
seq_region_name: 17
source: dbSNP
start: 73393244
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393253
feature_type: variation
id: rs1599518310
seq_region_name: 17
source: dbSNP
start: 73393253
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393253
feature_type: variation
id: rs2145502762
seq_region_name: 17
source: dbSNP
start: 73393253
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393253
feature_type: variation
id: rs2062943014
seq_region_name: 17
source: dbSNP
start: 73393254
strand: 1
-
alleles:
- A
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393254
feature_type: variation
id: rs1292976350
seq_region_name: 17
source: dbSNP
start: 73393254
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393254
feature_type: variation
id: rs2062943037
seq_region_name: 17
source: dbSNP
start: 73393254
strand: 1
-
alleles:
- AA
- AAGAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393255
feature_type: variation
id: rs2062943084
seq_region_name: 17
source: dbSNP
start: 73393254
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393254
feature_type: variation
id: rs1325552706
seq_region_name: 17
source: dbSNP
start: 73393255
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73393363
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393368
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393369
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393370
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393371
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393376
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393377
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393378
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393378
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73393380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599518534
seq_region_name: 17
source: dbSNP
start: 73393383
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393384
feature_type: variation
id: rs2062944499
seq_region_name: 17
source: dbSNP
start: 73393384
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393387
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393389
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393390
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393395
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393401
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393402
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393403
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393409
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393410
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393414
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73393416
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393418
feature_type: variation
id: rs1042510163
seq_region_name: 17
source: dbSNP
start: 73393418
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393419
feature_type: variation
id: rs923935094
seq_region_name: 17
source: dbSNP
start: 73393419
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393426
feature_type: variation
id: rs2062944787
seq_region_name: 17
source: dbSNP
start: 73393424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393425
feature_type: variation
id: rs565119879
seq_region_name: 17
source: dbSNP
start: 73393425
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393426
feature_type: variation
id: rs2062944832
seq_region_name: 17
source: dbSNP
start: 73393426
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393428
feature_type: variation
id: rs1243017760
seq_region_name: 17
source: dbSNP
start: 73393428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393431
feature_type: variation
id: rs1195983922
seq_region_name: 17
source: dbSNP
start: 73393431
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393435
feature_type: variation
id: rs113802137
seq_region_name: 17
source: dbSNP
start: 73393435
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393436
feature_type: variation
id: rs976564451
seq_region_name: 17
source: dbSNP
start: 73393436
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393441
feature_type: variation
id: rs2062944947
seq_region_name: 17
source: dbSNP
start: 73393441
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393449
feature_type: variation
id: rs2145503319
seq_region_name: 17
source: dbSNP
start: 73393449
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393452
feature_type: variation
id: rs1221183501
seq_region_name: 17
source: dbSNP
start: 73393452
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393453
feature_type: variation
id: rs922344087
seq_region_name: 17
source: dbSNP
start: 73393453
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393454
feature_type: variation
id: rs2062945008
seq_region_name: 17
source: dbSNP
start: 73393454
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393456
feature_type: variation
id: rs2062945030
seq_region_name: 17
source: dbSNP
start: 73393456
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393458
feature_type: variation
id: rs1293549022
seq_region_name: 17
source: dbSNP
start: 73393458
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393460
feature_type: variation
id: rs1241264264
seq_region_name: 17
source: dbSNP
start: 73393460
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393461
feature_type: variation
id: rs2145503366
seq_region_name: 17
source: dbSNP
start: 73393461
strand: 1
-
alleles:
- G
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393462
feature_type: variation
id: rs1258964158
seq_region_name: 17
source: dbSNP
start: 73393462
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393463
feature_type: variation
id: rs2062945121
seq_region_name: 17
source: dbSNP
start: 73393463
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393464
feature_type: variation
id: rs1485591045
seq_region_name: 17
source: dbSNP
start: 73393464
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393465
feature_type: variation
id: rs541537483
seq_region_name: 17
source: dbSNP
start: 73393465
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393466
feature_type: variation
id: rs1343490064
seq_region_name: 17
source: dbSNP
start: 73393466
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393468
feature_type: variation
id: rs2062945205
seq_region_name: 17
source: dbSNP
start: 73393468
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393471
feature_type: variation
id: rs1302464228
seq_region_name: 17
source: dbSNP
start: 73393471
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393472
feature_type: variation
id: rs370047423
seq_region_name: 17
source: dbSNP
start: 73393472
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393475
feature_type: variation
id: rs890053788
seq_region_name: 17
source: dbSNP
start: 73393475
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393478
feature_type: variation
id: rs2062945294
seq_region_name: 17
source: dbSNP
start: 73393478
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393481
feature_type: variation
id: rs2062945315
seq_region_name: 17
source: dbSNP
start: 73393478
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393486
feature_type: variation
id: rs2145503437
seq_region_name: 17
source: dbSNP
start: 73393486
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393491
feature_type: variation
id: rs2145503439
seq_region_name: 17
source: dbSNP
start: 73393491
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393499
feature_type: variation
id: rs2062945343
seq_region_name: 17
source: dbSNP
start: 73393499
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393500
feature_type: variation
id: rs1046725028
seq_region_name: 17
source: dbSNP
start: 73393500
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393501
feature_type: variation
id: rs1568379809
seq_region_name: 17
source: dbSNP
start: 73393501
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393510
feature_type: variation
id: rs1271630082
seq_region_name: 17
source: dbSNP
start: 73393510
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393511
feature_type: variation
id: rs2062945441
seq_region_name: 17
source: dbSNP
start: 73393511
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393512
feature_type: variation
id: rs1306435909
seq_region_name: 17
source: dbSNP
start: 73393512
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393514
feature_type: variation
id: rs1462788728
seq_region_name: 17
source: dbSNP
start: 73393512
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393515
feature_type: variation
id: rs375225747
seq_region_name: 17
source: dbSNP
start: 73393515
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393516
feature_type: variation
id: rs759954299
seq_region_name: 17
source: dbSNP
start: 73393516
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393517
feature_type: variation
id: rs768141552
seq_region_name: 17
source: dbSNP
start: 73393517
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393518
feature_type: variation
id: rs569668584
seq_region_name: 17
source: dbSNP
start: 73393518
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393521
feature_type: variation
id: rs1468608648
seq_region_name: 17
source: dbSNP
start: 73393521
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393522
feature_type: variation
id: rs752196606
seq_region_name: 17
source: dbSNP
start: 73393522
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393523
feature_type: variation
id: rs1418425337
seq_region_name: 17
source: dbSNP
start: 73393523
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393524
feature_type: variation
id: rs1041213712
seq_region_name: 17
source: dbSNP
start: 73393524
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393527
feature_type: variation
id: rs1476165071
seq_region_name: 17
source: dbSNP
start: 73393527
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393532
feature_type: variation
id: rs1429280873
seq_region_name: 17
source: dbSNP
start: 73393532
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393533
feature_type: variation
id: rs755707462
seq_region_name: 17
source: dbSNP
start: 73393533
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393535
feature_type: variation
id: rs2062945747
seq_region_name: 17
source: dbSNP
start: 73393535
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393536
feature_type: variation
id: rs200700910
seq_region_name: 17
source: dbSNP
start: 73393536
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393537
feature_type: variation
id: rs1410380205
seq_region_name: 17
source: dbSNP
start: 73393537
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393538
feature_type: variation
id: rs1330465599
seq_region_name: 17
source: dbSNP
start: 73393538
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393540
feature_type: variation
id: rs753403022
seq_region_name: 17
source: dbSNP
start: 73393540
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393541
feature_type: variation
id: rs901368128
seq_region_name: 17
source: dbSNP
start: 73393541
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393547
feature_type: variation
id: rs368973680
seq_region_name: 17
source: dbSNP
start: 73393547
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393549
feature_type: variation
id: rs745745779
seq_region_name: 17
source: dbSNP
start: 73393549
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393550
feature_type: variation
id: rs1202036836
seq_region_name: 17
source: dbSNP
start: 73393550
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: intron_variant
end: 73393551
feature_type: variation
id: rs202096378
seq_region_name: 17
source: dbSNP
start: 73393551
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73393552
feature_type: variation
id: rs201862701
seq_region_name: 17
source: dbSNP
start: 73393552
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73393559
feature_type: variation
id: rs748182538
seq_region_name: 17
source: dbSNP
start: 73393559
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393564
feature_type: variation
id: rs1356089715
seq_region_name: 17
source: dbSNP
start: 73393564
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393565
feature_type: variation
id: rs1196752497
seq_region_name: 17
source: dbSNP
start: 73393565
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393570
feature_type: variation
id: rs201343278
seq_region_name: 17
source: dbSNP
start: 73393570
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73393571
feature_type: variation
id: rs773386930
seq_region_name: 17
source: dbSNP
start: 73393571
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73393574
feature_type: variation
id: rs749455647
seq_region_name: 17
source: dbSNP
start: 73393574
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393575
feature_type: variation
id: rs771249786
seq_region_name: 17
source: dbSNP
start: 73393575
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393579
feature_type: variation
id: rs370932144
seq_region_name: 17
source: dbSNP
start: 73393579
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393585
feature_type: variation
id: rs1005852733
seq_region_name: 17
source: dbSNP
start: 73393585
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393588
feature_type: variation
id: rs759992297
seq_region_name: 17
source: dbSNP
start: 73393588
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393591
feature_type: variation
id: rs2062946352
seq_region_name: 17
source: dbSNP
start: 73393591
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393592
feature_type: variation
id: rs1016107268
seq_region_name: 17
source: dbSNP
start: 73393592
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393594
feature_type: variation
id: rs200464057
seq_region_name: 17
source: dbSNP
start: 73393594
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73393595
feature_type: variation
id: rs768088288
seq_region_name: 17
source: dbSNP
start: 73393595
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393597
feature_type: variation
id: rs959301788
seq_region_name: 17
source: dbSNP
start: 73393597
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393599
feature_type: variation
id: rs1169439995
seq_region_name: 17
source: dbSNP
start: 73393599
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393600
feature_type: variation
id: rs776172323
seq_region_name: 17
source: dbSNP
start: 73393600
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393601
feature_type: variation
id: rs761305278
seq_region_name: 17
source: dbSNP
start: 73393601
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393604
feature_type: variation
id: rs2062946592
seq_region_name: 17
source: dbSNP
start: 73393604
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393605
feature_type: variation
id: rs199620964
seq_region_name: 17
source: dbSNP
start: 73393605
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393606
feature_type: variation
id: rs753448445
seq_region_name: 17
source: dbSNP
start: 73393606
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393607
feature_type: variation
id: rs2062946703
seq_region_name: 17
source: dbSNP
start: 73393607
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393610
feature_type: variation
id: rs1441754107
seq_region_name: 17
source: dbSNP
start: 73393610
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393611
feature_type: variation
id: rs756858098
seq_region_name: 17
source: dbSNP
start: 73393611
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393612
feature_type: variation
id: rs764950234
seq_region_name: 17
source: dbSNP
start: 73393612
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393614
feature_type: variation
id: rs750130926
seq_region_name: 17
source: dbSNP
start: 73393614
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393615
feature_type: variation
id: rs2062946883
seq_region_name: 17
source: dbSNP
start: 73393615
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393616
feature_type: variation
id: rs758215851
seq_region_name: 17
source: dbSNP
start: 73393616
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393617
feature_type: variation
id: rs370092088
seq_region_name: 17
source: dbSNP
start: 73393617
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393627
feature_type: variation
id: rs2062946999
seq_region_name: 17
source: dbSNP
start: 73393627
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393632
feature_type: variation
id: rs2062947030
seq_region_name: 17
source: dbSNP
start: 73393632
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73393635
feature_type: variation
id: rs1272321576
seq_region_name: 17
source: dbSNP
start: 73393635
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393641
feature_type: variation
id: rs777650395
seq_region_name: 17
source: dbSNP
start: 73393641
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs749453108
seq_region_name: 17
source: dbSNP
start: 73393642
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2062947147
seq_region_name: 17
source: dbSNP
start: 73393643
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393644
feature_type: variation
id: rs1281384511
seq_region_name: 17
source: dbSNP
start: 73393644
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393647
feature_type: variation
id: rs1350137873
seq_region_name: 17
source: dbSNP
start: 73393647
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393650
feature_type: variation
id: rs1025216163
seq_region_name: 17
source: dbSNP
start: 73393650
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393651
feature_type: variation
id: rs771046841
seq_region_name: 17
source: dbSNP
start: 73393651
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393653
feature_type: variation
id: rs1481679150
seq_region_name: 17
source: dbSNP
start: 73393653
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393654
feature_type: variation
id: rs1256641105
seq_region_name: 17
source: dbSNP
start: 73393654
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393658
feature_type: variation
id: rs2145503868
seq_region_name: 17
source: dbSNP
start: 73393658
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73393659
feature_type: variation
id: rs2062947344
seq_region_name: 17
source: dbSNP
start: 73393659
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73393665
feature_type: variation
id: rs200982400
seq_region_name: 17
source: dbSNP
start: 73393665
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs373540507
seq_region_name: 17
source: dbSNP
start: 73393666
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393667
feature_type: variation
id: rs776018774
seq_region_name: 17
source: dbSNP
start: 73393667
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393668
feature_type: variation
id: rs2062947427
seq_region_name: 17
source: dbSNP
start: 73393668
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393669
feature_type: variation
id: rs2145503927
seq_region_name: 17
source: dbSNP
start: 73393669
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393676
feature_type: variation
id: rs761204864
seq_region_name: 17
source: dbSNP
start: 73393676
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393678
feature_type: variation
id: rs764665369
seq_region_name: 17
source: dbSNP
start: 73393678
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393680
feature_type: variation
id: rs144933006
seq_region_name: 17
source: dbSNP
start: 73393680
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs181533722
seq_region_name: 17
source: dbSNP
start: 73393682
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393683
feature_type: variation
id: rs147343958
seq_region_name: 17
source: dbSNP
start: 73393683
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393687
feature_type: variation
id: rs34322745
seq_region_name: 17
source: dbSNP
start: 73393687
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393688
feature_type: variation
id: rs1304776016
seq_region_name: 17
source: dbSNP
start: 73393688
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393690
feature_type: variation
id: rs1383238029
seq_region_name: 17
source: dbSNP
start: 73393690
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73393693
feature_type: variation
id: rs758072685
seq_region_name: 17
source: dbSNP
start: 73393693
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393695
feature_type: variation
id: rs2062947743
seq_region_name: 17
source: dbSNP
start: 73393695
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393697
feature_type: variation
id: rs766107690
seq_region_name: 17
source: dbSNP
start: 73393697
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393698
feature_type: variation
id: rs1434913508
seq_region_name: 17
source: dbSNP
start: 73393698
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393700
feature_type: variation
id: rs1599518996
seq_region_name: 17
source: dbSNP
start: 73393700
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393701
feature_type: variation
id: rs1304357221
seq_region_name: 17
source: dbSNP
start: 73393701
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393702
feature_type: variation
id: rs2145504067
seq_region_name: 17
source: dbSNP
start: 73393702
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393712
feature_type: variation
id: rs751363098
seq_region_name: 17
source: dbSNP
start: 73393712
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
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feature_type: variation
id: rs1232111611
seq_region_name: 17
source: dbSNP
start: 73393713
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393715
feature_type: variation
id: rs1255518469
seq_region_name: 17
source: dbSNP
start: 73393715
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393716
feature_type: variation
id: rs2145504103
seq_region_name: 17
source: dbSNP
start: 73393716
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393723
feature_type: variation
id: rs375662534
seq_region_name: 17
source: dbSNP
start: 73393723
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393726
feature_type: variation
id: rs770526832
seq_region_name: 17
source: dbSNP
start: 73393726
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393727
feature_type: variation
id: rs930164496
seq_region_name: 17
source: dbSNP
start: 73393727
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393730
feature_type: variation
id: rs534471511
seq_region_name: 17
source: dbSNP
start: 73393730
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73393732
feature_type: variation
id: rs982474312
seq_region_name: 17
source: dbSNP
start: 73393732
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393742
feature_type: variation
id: rs1194045918
seq_region_name: 17
source: dbSNP
start: 73393742
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393743
feature_type: variation
id: rs1254439033
seq_region_name: 17
source: dbSNP
start: 73393743
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73393744
feature_type: variation
id: rs546684021
seq_region_name: 17
source: dbSNP
start: 73393744
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393746
feature_type: variation
id: rs1192665270
seq_region_name: 17
source: dbSNP
start: 73393746
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393748
feature_type: variation
id: rs2062948243
seq_region_name: 17
source: dbSNP
start: 73393748
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73393749
feature_type: variation
id: rs757398922
seq_region_name: 17
source: dbSNP
start: 73393749
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73393754
feature_type: variation
id: rs778890310
seq_region_name: 17
source: dbSNP
start: 73393754
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73393755
feature_type: variation
id: rs2062948331
seq_region_name: 17
source: dbSNP
start: 73393755
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73393757
feature_type: variation
id: rs746036794
seq_region_name: 17
source: dbSNP
start: 73393757
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73393759
feature_type: variation
id: rs1383442049
seq_region_name: 17
source: dbSNP
start: 73393759
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73393764
feature_type: variation
id: rs370242961
seq_region_name: 17
source: dbSNP
start: 73393764
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73393766
feature_type: variation
id: rs1463361333
seq_region_name: 17
source: dbSNP
start: 73393766
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393767
feature_type: variation
id: rs780497799
seq_region_name: 17
source: dbSNP
start: 73393767
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393768
feature_type: variation
id: rs201417060
seq_region_name: 17
source: dbSNP
start: 73393768
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393769
feature_type: variation
id: rs1408034922
seq_region_name: 17
source: dbSNP
start: 73393769
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393772
feature_type: variation
id: rs2145504237
seq_region_name: 17
source: dbSNP
start: 73393772
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393774
feature_type: variation
id: rs769027440
seq_region_name: 17
source: dbSNP
start: 73393774
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393778
feature_type: variation
id: rs1599519093
seq_region_name: 17
source: dbSNP
start: 73393778
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393781
feature_type: variation
id: rs2145504260
seq_region_name: 17
source: dbSNP
start: 73393781
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393783
feature_type: variation
id: rs777241078
seq_region_name: 17
source: dbSNP
start: 73393783
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393787
feature_type: variation
id: rs761192545
seq_region_name: 17
source: dbSNP
start: 73393787
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393788
feature_type: variation
id: rs769302870
seq_region_name: 17
source: dbSNP
start: 73393788
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393789
feature_type: variation
id: rs2145504288
seq_region_name: 17
source: dbSNP
start: 73393789
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393796
feature_type: variation
id: rs776024759
seq_region_name: 17
source: dbSNP
start: 73393796
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393798
feature_type: variation
id: rs376018446
seq_region_name: 17
source: dbSNP
start: 73393798
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393800
feature_type: variation
id: rs1184041819
seq_region_name: 17
source: dbSNP
start: 73393800
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393801
feature_type: variation
id: rs1462474794
seq_region_name: 17
source: dbSNP
start: 73393801
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393803
feature_type: variation
id: rs1015864785
seq_region_name: 17
source: dbSNP
start: 73393803
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393805
feature_type: variation
id: rs1178038216
seq_region_name: 17
source: dbSNP
start: 73393805
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393808
feature_type: variation
id: rs1214941726
seq_region_name: 17
source: dbSNP
start: 73393808
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393811
feature_type: variation
id: rs2062948758
seq_region_name: 17
source: dbSNP
start: 73393811
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393812
feature_type: variation
id: rs1426763765
seq_region_name: 17
source: dbSNP
start: 73393812
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393813
feature_type: variation
id: rs558383586
seq_region_name: 17
source: dbSNP
start: 73393813
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393819
feature_type: variation
id: rs1599519154
seq_region_name: 17
source: dbSNP
start: 73393819
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393822
feature_type: variation
id: rs1315991583
seq_region_name: 17
source: dbSNP
start: 73393822
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393825
feature_type: variation
id: rs1170959251
seq_region_name: 17
source: dbSNP
start: 73393822
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393824
feature_type: variation
id: rs1568380022
seq_region_name: 17
source: dbSNP
start: 73393824
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393828
feature_type: variation
id: rs1012116569
seq_region_name: 17
source: dbSNP
start: 73393828
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393831
feature_type: variation
id: rs1444850751
seq_region_name: 17
source: dbSNP
start: 73393831
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393833
feature_type: variation
id: rs78797306
seq_region_name: 17
source: dbSNP
start: 73393833
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393837
feature_type: variation
id: rs970932065
seq_region_name: 17
source: dbSNP
start: 73393837
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393839
feature_type: variation
id: rs906676246
seq_region_name: 17
source: dbSNP
start: 73393839
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393841
feature_type: variation
id: rs2145504402
seq_region_name: 17
source: dbSNP
start: 73393841
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73393845
feature_type: variation
id: rs2062949075
seq_region_name: 17
source: dbSNP
start: 73393845
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73394006
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394017
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394022
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394029
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394030
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394031
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394032
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73394035
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394041
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394042
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394043
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394048
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394051
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394052
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394057
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1421254715
seq_region_name: 17
source: dbSNP
start: 73394058
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394059
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394061
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394062
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394063
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394065
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394068
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394070
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394076
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73394078
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394080
feature_type: variation
id: rs181774083
seq_region_name: 17
source: dbSNP
start: 73394080
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394081
feature_type: variation
id: rs1269648405
seq_region_name: 17
source: dbSNP
start: 73394081
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394082
feature_type: variation
id: rs2062950684
seq_region_name: 17
source: dbSNP
start: 73394082
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394086
feature_type: variation
id: rs1225021332
seq_region_name: 17
source: dbSNP
start: 73394085
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394086
feature_type: variation
id: rs1479742034
seq_region_name: 17
source: dbSNP
start: 73394086
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394092
feature_type: variation
id: rs1343676601
seq_region_name: 17
source: dbSNP
start: 73394092
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394094
feature_type: variation
id: rs546121460
seq_region_name: 17
source: dbSNP
start: 73394094
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599519404
seq_region_name: 17
source: dbSNP
start: 73394097
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062950811
seq_region_name: 17
source: dbSNP
start: 73394098
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1250964688
seq_region_name: 17
source: dbSNP
start: 73394100
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394101
feature_type: variation
id: rs948322857
seq_region_name: 17
source: dbSNP
start: 73394101
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394102
feature_type: variation
id: rs79979395
seq_region_name: 17
source: dbSNP
start: 73394102
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394104
feature_type: variation
id: rs1404456436
seq_region_name: 17
source: dbSNP
start: 73394104
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394113
feature_type: variation
id: rs1270966372
seq_region_name: 17
source: dbSNP
start: 73394112
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394114
feature_type: variation
id: rs982366071
seq_region_name: 17
source: dbSNP
start: 73394114
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394117
feature_type: variation
id: rs528328864
seq_region_name: 17
source: dbSNP
start: 73394117
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394118
feature_type: variation
id: rs2062950994
seq_region_name: 17
source: dbSNP
start: 73394118
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394124
feature_type: variation
id: rs935476545
seq_region_name: 17
source: dbSNP
start: 73394124
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394126
feature_type: variation
id: rs1052558764
seq_region_name: 17
source: dbSNP
start: 73394126
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394128
feature_type: variation
id: rs1037447831
seq_region_name: 17
source: dbSNP
start: 73394128
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394129
feature_type: variation
id: rs1599519449
seq_region_name: 17
source: dbSNP
start: 73394129
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394133
feature_type: variation
id: rs1388161106
seq_region_name: 17
source: dbSNP
start: 73394133
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394138
feature_type: variation
id: rs1212582227
seq_region_name: 17
source: dbSNP
start: 73394138
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394139
feature_type: variation
id: rs1294501007
seq_region_name: 17
source: dbSNP
start: 73394139
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394142
feature_type: variation
id: rs1297241797
seq_region_name: 17
source: dbSNP
start: 73394142
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394143
feature_type: variation
id: rs774105812
seq_region_name: 17
source: dbSNP
start: 73394143
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394148
feature_type: variation
id: rs893899786
seq_region_name: 17
source: dbSNP
start: 73394148
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394150
feature_type: variation
id: rs1224562277
seq_region_name: 17
source: dbSNP
start: 73394150
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394152
feature_type: variation
id: rs1296048529
seq_region_name: 17
source: dbSNP
start: 73394152
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394153
feature_type: variation
id: rs2062951286
seq_region_name: 17
source: dbSNP
start: 73394153
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394154
feature_type: variation
id: rs1402163075
seq_region_name: 17
source: dbSNP
start: 73394154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394160
feature_type: variation
id: rs2062951303
seq_region_name: 17
source: dbSNP
start: 73394160
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394164
feature_type: variation
id: rs766089168
seq_region_name: 17
source: dbSNP
start: 73394164
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394166
feature_type: variation
id: rs368550768
seq_region_name: 17
source: dbSNP
start: 73394166
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394167
feature_type: variation
id: rs372615667
seq_region_name: 17
source: dbSNP
start: 73394167
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394169
feature_type: variation
id: rs1208855208
seq_region_name: 17
source: dbSNP
start: 73394169
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394172
feature_type: variation
id: rs2062951432
seq_region_name: 17
source: dbSNP
start: 73394172
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394174
feature_type: variation
id: rs375839111
seq_region_name: 17
source: dbSNP
start: 73394174
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394175
feature_type: variation
id: rs1417384060
seq_region_name: 17
source: dbSNP
start: 73394175
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394178
feature_type: variation
id: rs756027890
seq_region_name: 17
source: dbSNP
start: 73394178
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394181
feature_type: variation
id: rs1179060765
seq_region_name: 17
source: dbSNP
start: 73394181
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394182
feature_type: variation
id: rs750443165
seq_region_name: 17
source: dbSNP
start: 73394182
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394184
feature_type: variation
id: rs1250136757
seq_region_name: 17
source: dbSNP
start: 73394184
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394185
feature_type: variation
id: rs779077145
seq_region_name: 17
source: dbSNP
start: 73394185
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394186
feature_type: variation
id: rs1166335853
seq_region_name: 17
source: dbSNP
start: 73394186
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394187
feature_type: variation
id: rs1397110481
seq_region_name: 17
source: dbSNP
start: 73394187
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394189
feature_type: variation
id: rs750534193
seq_region_name: 17
source: dbSNP
start: 73394189
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394190
feature_type: variation
id: rs780479295
seq_region_name: 17
source: dbSNP
start: 73394190
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394193
feature_type: variation
id: rs1397506088
seq_region_name: 17
source: dbSNP
start: 73394193
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394194
feature_type: variation
id: rs1393167050
seq_region_name: 17
source: dbSNP
start: 73394194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394199
feature_type: variation
id: rs73345967
seq_region_name: 17
source: dbSNP
start: 73394199
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394200
feature_type: variation
id: rs769100655
seq_region_name: 17
source: dbSNP
start: 73394200
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73394204
feature_type: variation
id: rs1261601977
seq_region_name: 17
source: dbSNP
start: 73394204
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394209
feature_type: variation
id: rs781437461
seq_region_name: 17
source: dbSNP
start: 73394209
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394210
feature_type: variation
id: rs1203604538
seq_region_name: 17
source: dbSNP
start: 73394210
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394212
feature_type: variation
id: rs1295117563
seq_region_name: 17
source: dbSNP
start: 73394212
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394213
feature_type: variation
id: rs1332405481
seq_region_name: 17
source: dbSNP
start: 73394213
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394214
feature_type: variation
id: rs1243800717
seq_region_name: 17
source: dbSNP
start: 73394214
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394215
feature_type: variation
id: rs1265541402
seq_region_name: 17
source: dbSNP
start: 73394215
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394216
feature_type: variation
id: rs2062951957
seq_region_name: 17
source: dbSNP
start: 73394216
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394218
feature_type: variation
id: rs748634086
seq_region_name: 17
source: dbSNP
start: 73394218
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394219
feature_type: variation
id: rs1481423189
seq_region_name: 17
source: dbSNP
start: 73394219
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394223
feature_type: variation
id: rs770209140
seq_region_name: 17
source: dbSNP
start: 73394223
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394224
feature_type: variation
id: rs142553153
seq_region_name: 17
source: dbSNP
start: 73394224
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394227
feature_type: variation
id: rs904381
seq_region_name: 17
source: dbSNP
start: 73394227
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394229
feature_type: variation
id: rs1189267952
seq_region_name: 17
source: dbSNP
start: 73394229
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394230
feature_type: variation
id: rs372758501
seq_region_name: 17
source: dbSNP
start: 73394230
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394231
feature_type: variation
id: rs1422378748
seq_region_name: 17
source: dbSNP
start: 73394231
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394234
feature_type: variation
id: rs376746309
seq_region_name: 17
source: dbSNP
start: 73394234
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394235
feature_type: variation
id: rs759143958
seq_region_name: 17
source: dbSNP
start: 73394235
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394237
feature_type: variation
id: rs1262639231
seq_region_name: 17
source: dbSNP
start: 73394237
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394239
feature_type: variation
id: rs2145505394
seq_region_name: 17
source: dbSNP
start: 73394239
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394240
feature_type: variation
id: rs2062952340
seq_region_name: 17
source: dbSNP
start: 73394240
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394244
feature_type: variation
id: rs369218969
seq_region_name: 17
source: dbSNP
start: 73394244
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394245
feature_type: variation
id: rs371857762
seq_region_name: 17
source: dbSNP
start: 73394245
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394246
feature_type: variation
id: rs1370015938
seq_region_name: 17
source: dbSNP
start: 73394246
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394248
feature_type: variation
id: rs760592944
seq_region_name: 17
source: dbSNP
start: 73394248
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394249
feature_type: variation
id: rs991229722
seq_region_name: 17
source: dbSNP
start: 73394249
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394253
feature_type: variation
id: rs764192799
seq_region_name: 17
source: dbSNP
start: 73394253
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394254
feature_type: variation
id: rs1353497802
seq_region_name: 17
source: dbSNP
start: 73394254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73394257
feature_type: variation
id: rs750515841
seq_region_name: 17
source: dbSNP
start: 73394257
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73394258
feature_type: variation
id: rs1296061486
seq_region_name: 17
source: dbSNP
start: 73394258
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394261
feature_type: variation
id: rs758597712
seq_region_name: 17
source: dbSNP
start: 73394261
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394262
feature_type: variation
id: rs752844828
seq_region_name: 17
source: dbSNP
start: 73394262
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394263
feature_type: variation
id: rs1273539134
seq_region_name: 17
source: dbSNP
start: 73394263
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394265
feature_type: variation
id: rs1241693104
seq_region_name: 17
source: dbSNP
start: 73394265
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394270
feature_type: variation
id: rs780389326
seq_region_name: 17
source: dbSNP
start: 73394270
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394271
feature_type: variation
id: rs751760843
seq_region_name: 17
source: dbSNP
start: 73394271
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394272
feature_type: variation
id: rs1260173620
seq_region_name: 17
source: dbSNP
start: 73394272
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394275
feature_type: variation
id: rs755173242
seq_region_name: 17
source: dbSNP
start: 73394275
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394279
feature_type: variation
id: rs2062952823
seq_region_name: 17
source: dbSNP
start: 73394279
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394281
feature_type: variation
id: rs1462037916
seq_region_name: 17
source: dbSNP
start: 73394281
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394285
feature_type: variation
id: rs1181831361
seq_region_name: 17
source: dbSNP
start: 73394285
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394291
feature_type: variation
id: rs1262840192
seq_region_name: 17
source: dbSNP
start: 73394291
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394296
feature_type: variation
id: rs781557111
seq_region_name: 17
source: dbSNP
start: 73394296
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394297
feature_type: variation
id: rs748530818
seq_region_name: 17
source: dbSNP
start: 73394297
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394299
feature_type: variation
id: rs2062952986
seq_region_name: 17
source: dbSNP
start: 73394299
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394300
feature_type: variation
id: rs2062953014
seq_region_name: 17
source: dbSNP
start: 73394300
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394301
feature_type: variation
id: rs2062953046
seq_region_name: 17
source: dbSNP
start: 73394301
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394303
feature_type: variation
id: rs1389787563
seq_region_name: 17
source: dbSNP
start: 73394303
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394304
feature_type: variation
id: rs2062953098
seq_region_name: 17
source: dbSNP
start: 73394304
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394306
feature_type: variation
id: rs2062953117
seq_region_name: 17
source: dbSNP
start: 73394306
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394308
feature_type: variation
id: rs75044137
seq_region_name: 17
source: dbSNP
start: 73394308
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394311
feature_type: variation
id: rs756633246
seq_region_name: 17
source: dbSNP
start: 73394311
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73394313
feature_type: variation
id: rs752695536
seq_region_name: 17
source: dbSNP
start: 73394313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394314
feature_type: variation
id: rs971071570
seq_region_name: 17
source: dbSNP
start: 73394314
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394318
feature_type: variation
id: rs2145505662
seq_region_name: 17
source: dbSNP
start: 73394318
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73394320
feature_type: variation
id: rs2145505669
seq_region_name: 17
source: dbSNP
start: 73394320
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73394322
feature_type: variation
id: rs1465452863
seq_region_name: 17
source: dbSNP
start: 73394322
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73394323
feature_type: variation
id: rs2145505686
seq_region_name: 17
source: dbSNP
start: 73394323
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73394327
feature_type: variation
id: rs1289421085
seq_region_name: 17
source: dbSNP
start: 73394327
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73394328
feature_type: variation
id: rs982804810
seq_region_name: 17
source: dbSNP
start: 73394328
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73394329
feature_type: variation
id: rs1018377143
seq_region_name: 17
source: dbSNP
start: 73394329
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73394330
feature_type: variation
id: rs1383216030
seq_region_name: 17
source: dbSNP
start: 73394330
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73394332
feature_type: variation
id: rs1296348350
seq_region_name: 17
source: dbSNP
start: 73394332
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73394333
feature_type: variation
id: rs758201939
seq_region_name: 17
source: dbSNP
start: 73394333
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73394338
feature_type: variation
id: rs369147847
seq_region_name: 17
source: dbSNP
start: 73394338
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73394339
feature_type: variation
id: rs7220954
seq_region_name: 17
source: dbSNP
start: 73394339
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394342
feature_type: variation
id: rs1345196678
seq_region_name: 17
source: dbSNP
start: 73394342
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394343
feature_type: variation
id: rs988317222
seq_region_name: 17
source: dbSNP
start: 73394343
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394344
feature_type: variation
id: rs915385569
seq_region_name: 17
source: dbSNP
start: 73394344
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394347
feature_type: variation
id: rs1277533763
seq_region_name: 17
source: dbSNP
start: 73394347
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394351
feature_type: variation
id: rs1311156951
seq_region_name: 17
source: dbSNP
start: 73394351
strand: 1
-
alleles:
- TCAGGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394361
feature_type: variation
id: rs1163152772
seq_region_name: 17
source: dbSNP
start: 73394356
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394357
feature_type: variation
id: rs2062953668
seq_region_name: 17
source: dbSNP
start: 73394357
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394358
feature_type: variation
id: rs2062953694
seq_region_name: 17
source: dbSNP
start: 73394359
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394359
feature_type: variation
id: rs2062953715
seq_region_name: 17
source: dbSNP
start: 73394359
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394360
feature_type: variation
id: rs1210016424
seq_region_name: 17
source: dbSNP
start: 73394360
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394361
feature_type: variation
id: rs2062953759
seq_region_name: 17
source: dbSNP
start: 73394361
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394362
feature_type: variation
id: rs374660564
seq_region_name: 17
source: dbSNP
start: 73394362
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394363
feature_type: variation
id: rs745465438
seq_region_name: 17
source: dbSNP
start: 73394363
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394365
feature_type: variation
id: rs369851292
seq_region_name: 17
source: dbSNP
start: 73394365
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394366
feature_type: variation
id: rs2062953865
seq_region_name: 17
source: dbSNP
start: 73394366
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394367
feature_type: variation
id: rs367788655
seq_region_name: 17
source: dbSNP
start: 73394367
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394368
feature_type: variation
id: rs983468307
seq_region_name: 17
source: dbSNP
start: 73394368
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394369
feature_type: variation
id: rs186470701
seq_region_name: 17
source: dbSNP
start: 73394369
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394377
feature_type: variation
id: rs1216775043
seq_region_name: 17
source: dbSNP
start: 73394377
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394378
feature_type: variation
id: rs2062953979
seq_region_name: 17
source: dbSNP
start: 73394378
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394379
feature_type: variation
id: rs756835634
seq_region_name: 17
source: dbSNP
start: 73394379
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394384
feature_type: variation
id: rs1716483247
seq_region_name: 17
source: dbSNP
start: 73394384
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394385
feature_type: variation
id: rs558834879
seq_region_name: 17
source: dbSNP
start: 73394385
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394387
feature_type: variation
id: rs1555758497
seq_region_name: 17
source: dbSNP
start: 73394387
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394390
feature_type: variation
id: rs916344457
seq_region_name: 17
source: dbSNP
start: 73394390
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394391
feature_type: variation
id: rs947700792
seq_region_name: 17
source: dbSNP
start: 73394391
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394392
feature_type: variation
id: rs571049655
seq_region_name: 17
source: dbSNP
start: 73394392
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394395
feature_type: variation
id: rs1046045646
seq_region_name: 17
source: dbSNP
start: 73394395
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394398
feature_type: variation
id: rs887032843
seq_region_name: 17
source: dbSNP
start: 73394398
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394400
feature_type: variation
id: rs1285675255
seq_region_name: 17
source: dbSNP
start: 73394400
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394401
feature_type: variation
id: rs1225154372
seq_region_name: 17
source: dbSNP
start: 73394401
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394403
feature_type: variation
id: rs906218321
seq_region_name: 17
source: dbSNP
start: 73394403
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394404
feature_type: variation
id: rs1401981382
seq_region_name: 17
source: dbSNP
start: 73394404
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394405
feature_type: variation
id: rs1363760399
seq_region_name: 17
source: dbSNP
start: 73394405
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394406
feature_type: variation
id: rs780936495
seq_region_name: 17
source: dbSNP
start: 73394406
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394409
feature_type: variation
id: rs1425485904
seq_region_name: 17
source: dbSNP
start: 73394409
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394413
feature_type: variation
id: rs2062954269
seq_region_name: 17
source: dbSNP
start: 73394413
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394414
feature_type: variation
id: rs1416429462
seq_region_name: 17
source: dbSNP
start: 73394414
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394416
feature_type: variation
id: rs1166450912
seq_region_name: 17
source: dbSNP
start: 73394416
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394422
feature_type: variation
id: rs114374323
seq_region_name: 17
source: dbSNP
start: 73394422
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394423
feature_type: variation
id: rs1374197865
seq_region_name: 17
source: dbSNP
start: 73394423
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394425
feature_type: variation
id: rs1478533881
seq_region_name: 17
source: dbSNP
start: 73394425
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394427
feature_type: variation
id: rs893605853
seq_region_name: 17
source: dbSNP
start: 73394427
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394431
feature_type: variation
id: rs2062954395
seq_region_name: 17
source: dbSNP
start: 73394430
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394431
feature_type: variation
id: rs2062954417
seq_region_name: 17
source: dbSNP
start: 73394431
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394435
feature_type: variation
id: rs2062954437
seq_region_name: 17
source: dbSNP
start: 73394435
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394437
feature_type: variation
id: rs2062954464
seq_region_name: 17
source: dbSNP
start: 73394437
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394438
feature_type: variation
id: rs2062954481
seq_region_name: 17
source: dbSNP
start: 73394438
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394444
feature_type: variation
id: rs1444489819
seq_region_name: 17
source: dbSNP
start: 73394444
strand: 1
-
alleles:
- AAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394446
feature_type: variation
id: rs1266086042
seq_region_name: 17
source: dbSNP
start: 73394444
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394447
feature_type: variation
id: rs2062954556
seq_region_name: 17
source: dbSNP
start: 73394447
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394448
feature_type: variation
id: rs1013107012
seq_region_name: 17
source: dbSNP
start: 73394448
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394453
feature_type: variation
id: rs2145506053
seq_region_name: 17
source: dbSNP
start: 73394453
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394454
feature_type: variation
id: rs1451748765
seq_region_name: 17
source: dbSNP
start: 73394454
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394457
feature_type: variation
id: rs745365538
seq_region_name: 17
source: dbSNP
start: 73394457
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394458
feature_type: variation
id: rs2062954656
seq_region_name: 17
source: dbSNP
start: 73394458
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394463
feature_type: variation
id: rs1010754005
seq_region_name: 17
source: dbSNP
start: 73394463
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394469
feature_type: variation
id: rs1410185966
seq_region_name: 17
source: dbSNP
start: 73394469
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73394705
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73394710
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394711
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394722
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394723
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394727
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394729
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394731
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394733
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394737
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394740
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73394945
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73394950
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73394953
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73394968
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73394976
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394986
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73394987
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1340611587
seq_region_name: 17
source: dbSNP
start: 73394988
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062958226
seq_region_name: 17
source: dbSNP
start: 73394990
strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1022546978
seq_region_name: 17
source: dbSNP
start: 73394990
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394992
feature_type: variation
id: rs2062958264
seq_region_name: 17
source: dbSNP
start: 73394992
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394993
feature_type: variation
id: rs2173426
seq_region_name: 17
source: dbSNP
start: 73394993
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394994
feature_type: variation
id: rs1269641879
seq_region_name: 17
source: dbSNP
start: 73394994
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394996
feature_type: variation
id: rs182292394
seq_region_name: 17
source: dbSNP
start: 73394996
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394997
feature_type: variation
id: rs1293728305
seq_region_name: 17
source: dbSNP
start: 73394997
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394998
feature_type: variation
id: rs972010926
seq_region_name: 17
source: dbSNP
start: 73394998
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73394999
feature_type: variation
id: rs745599253
seq_region_name: 17
source: dbSNP
start: 73394999
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395001
feature_type: variation
id: rs2062958408
seq_region_name: 17
source: dbSNP
start: 73395001
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395005
feature_type: variation
id: rs2062958433
seq_region_name: 17
source: dbSNP
start: 73395005
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395007
feature_type: variation
id: rs2062958458
seq_region_name: 17
source: dbSNP
start: 73395007
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395011
feature_type: variation
id: rs2062958484
seq_region_name: 17
source: dbSNP
start: 73395011
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395013
feature_type: variation
id: rs571151408
seq_region_name: 17
source: dbSNP
start: 73395013
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395016
feature_type: variation
id: rs2062958529
seq_region_name: 17
source: dbSNP
start: 73395016
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395019
feature_type: variation
id: rs1475612946
seq_region_name: 17
source: dbSNP
start: 73395019
strand: 1
-
alleles:
- "-"
- T
- TGTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395020
feature_type: variation
id: rs1169502697
seq_region_name: 17
source: dbSNP
start: 73395021
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395021
feature_type: variation
id: rs927713307
seq_region_name: 17
source: dbSNP
start: 73395021
strand: 1
-
alleles:
- "-"
- TCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395021
feature_type: variation
id: rs1394071779
seq_region_name: 17
source: dbSNP
start: 73395022
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395022
feature_type: variation
id: rs1425880624
seq_region_name: 17
source: dbSNP
start: 73395022
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395027
feature_type: variation
id: rs2062958655
seq_region_name: 17
source: dbSNP
start: 73395027
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395032
feature_type: variation
id: rs1409239125
seq_region_name: 17
source: dbSNP
start: 73395032
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395033
feature_type: variation
id: rs2062958691
seq_region_name: 17
source: dbSNP
start: 73395033
strand: 1
-
alleles:
- ATGAGCTCAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395045
feature_type: variation
id: rs2062958719
seq_region_name: 17
source: dbSNP
start: 73395036
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395038
feature_type: variation
id: rs934984880
seq_region_name: 17
source: dbSNP
start: 73395038
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395044
feature_type: variation
id: rs2062958738
seq_region_name: 17
source: dbSNP
start: 73395044
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395047
feature_type: variation
id: rs1268380601
seq_region_name: 17
source: dbSNP
start: 73395047
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395053
feature_type: variation
id: rs2062958760
seq_region_name: 17
source: dbSNP
start: 73395053
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395058
feature_type: variation
id: rs2062958795
seq_region_name: 17
source: dbSNP
start: 73395058
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395063
feature_type: variation
id: rs534991635
seq_region_name: 17
source: dbSNP
start: 73395063
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395070
feature_type: variation
id: rs547239390
seq_region_name: 17
source: dbSNP
start: 73395070
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395072
feature_type: variation
id: rs1282218026
seq_region_name: 17
source: dbSNP
start: 73395072
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395074
feature_type: variation
id: rs955500978
seq_region_name: 17
source: dbSNP
start: 73395074
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395077
feature_type: variation
id: rs568583229
seq_region_name: 17
source: dbSNP
start: 73395077
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395078
feature_type: variation
id: rs146229407
seq_region_name: 17
source: dbSNP
start: 73395078
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395079
feature_type: variation
id: rs17782141
seq_region_name: 17
source: dbSNP
start: 73395079
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395080
feature_type: variation
id: rs940015298
seq_region_name: 17
source: dbSNP
start: 73395080
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395081
feature_type: variation
id: rs2062959058
seq_region_name: 17
source: dbSNP
start: 73395081
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395083
feature_type: variation
id: rs1205026190
seq_region_name: 17
source: dbSNP
start: 73395083
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395087
feature_type: variation
id: rs575805376
seq_region_name: 17
source: dbSNP
start: 73395087
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395090
feature_type: variation
id: rs539869089
seq_region_name: 17
source: dbSNP
start: 73395090
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395092
feature_type: variation
id: rs139299054
seq_region_name: 17
source: dbSNP
start: 73395092
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395101
feature_type: variation
id: rs2062959177
seq_region_name: 17
source: dbSNP
start: 73395101
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395102
feature_type: variation
id: rs1378222829
seq_region_name: 17
source: dbSNP
start: 73395102
strand: 1
-
alleles:
- AGAGA
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395106
feature_type: variation
id: rs948608750
seq_region_name: 17
source: dbSNP
start: 73395102
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395106
feature_type: variation
id: rs1417485844
seq_region_name: 17
source: dbSNP
start: 73395106
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395108
feature_type: variation
id: rs1178520328
seq_region_name: 17
source: dbSNP
start: 73395107
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395112
feature_type: variation
id: rs1423121119
seq_region_name: 17
source: dbSNP
start: 73395112
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395114
feature_type: variation
id: rs776745744
seq_region_name: 17
source: dbSNP
start: 73395114
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395117
feature_type: variation
id: rs1414033021
seq_region_name: 17
source: dbSNP
start: 73395114
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395115
feature_type: variation
id: rs761869303
seq_region_name: 17
source: dbSNP
start: 73395115
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395116
feature_type: variation
id: rs1455403055
seq_region_name: 17
source: dbSNP
start: 73395116
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395119
feature_type: variation
id: rs2062959406
seq_region_name: 17
source: dbSNP
start: 73395119
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395122
feature_type: variation
id: rs1319684159
seq_region_name: 17
source: dbSNP
start: 73395122
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395123
feature_type: variation
id: rs1395001622
seq_region_name: 17
source: dbSNP
start: 73395123
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395124
feature_type: variation
id: rs751366982
seq_region_name: 17
source: dbSNP
start: 73395124
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395126
feature_type: variation
id: rs2062959508
seq_region_name: 17
source: dbSNP
start: 73395126
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395131
feature_type: variation
id: rs1599520690
seq_region_name: 17
source: dbSNP
start: 73395131
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395132
feature_type: variation
id: rs938471186
seq_region_name: 17
source: dbSNP
start: 73395132
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395136
feature_type: variation
id: rs2062959573
seq_region_name: 17
source: dbSNP
start: 73395136
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395138
feature_type: variation
id: rs1442620938
seq_region_name: 17
source: dbSNP
start: 73395138
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395139
feature_type: variation
id: rs1300878591
seq_region_name: 17
source: dbSNP
start: 73395139
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395140
feature_type: variation
id: rs1366287978
seq_region_name: 17
source: dbSNP
start: 73395140
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395142
feature_type: variation
id: rs374102511
seq_region_name: 17
source: dbSNP
start: 73395142
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395142
feature_type: variation
id: rs1343705527
seq_region_name: 17
source: dbSNP
start: 73395142
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395143
feature_type: variation
id: rs751599592
seq_region_name: 17
source: dbSNP
start: 73395143
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395147
feature_type: variation
id: rs1568380575
seq_region_name: 17
source: dbSNP
start: 73395144
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395145
feature_type: variation
id: rs1308264010
seq_region_name: 17
source: dbSNP
start: 73395145
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395146
feature_type: variation
id: rs755227285
seq_region_name: 17
source: dbSNP
start: 73395146
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395147
feature_type: variation
id: rs573154539
seq_region_name: 17
source: dbSNP
start: 73395147
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395148
feature_type: variation
id: rs753084965
seq_region_name: 17
source: dbSNP
start: 73395148
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73395150
feature_type: variation
id: rs1469225924
seq_region_name: 17
source: dbSNP
start: 73395150
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73395151
feature_type: variation
id: rs756511777
seq_region_name: 17
source: dbSNP
start: 73395151
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73395154
feature_type: variation
id: rs1314833290
seq_region_name: 17
source: dbSNP
start: 73395154
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395156
feature_type: variation
id: rs1308060454
seq_region_name: 17
source: dbSNP
start: 73395156
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395158
feature_type: variation
id: rs1599520779
seq_region_name: 17
source: dbSNP
start: 73395158
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395159
feature_type: variation
id: rs778143441
seq_region_name: 17
source: dbSNP
start: 73395159
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73395161
feature_type: variation
id: rs2062960070
seq_region_name: 17
source: dbSNP
start: 73395161
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73395163
feature_type: variation
id: rs140824189
seq_region_name: 17
source: dbSNP
start: 73395163
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395164
feature_type: variation
id: rs757774349
seq_region_name: 17
source: dbSNP
start: 73395164
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395171
feature_type: variation
id: rs1410025480
seq_region_name: 17
source: dbSNP
start: 73395171
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395173
feature_type: variation
id: rs1471553992
seq_region_name: 17
source: dbSNP
start: 73395173
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395175
feature_type: variation
id: rs1599520804
seq_region_name: 17
source: dbSNP
start: 73395175
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395177
feature_type: variation
id: rs376942765
seq_region_name: 17
source: dbSNP
start: 73395177
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73395180
feature_type: variation
id: rs375688906
seq_region_name: 17
source: dbSNP
start: 73395180
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395181
feature_type: variation
id: rs149731522
seq_region_name: 17
source: dbSNP
start: 73395181
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395182
feature_type: variation
id: rs746785926
seq_region_name: 17
source: dbSNP
start: 73395182
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395183
feature_type: variation
id: rs1348955170
seq_region_name: 17
source: dbSNP
start: 73395183
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395184
feature_type: variation
id: rs768527388
seq_region_name: 17
source: dbSNP
start: 73395184
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73395185
feature_type: variation
id: rs1299414090
seq_region_name: 17
source: dbSNP
start: 73395185
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73395194
feature_type: variation
id: rs2062960435
seq_region_name: 17
source: dbSNP
start: 73395192
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395194
feature_type: variation
id: rs1379967932
seq_region_name: 17
source: dbSNP
start: 73395194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395197
feature_type: variation
id: rs1348129066
seq_region_name: 17
source: dbSNP
start: 73395197
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395198
feature_type: variation
id: rs146726977
seq_region_name: 17
source: dbSNP
start: 73395198
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395200
feature_type: variation
id: rs2062960580
seq_region_name: 17
source: dbSNP
start: 73395200
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395201
feature_type: variation
id: rs140373513
seq_region_name: 17
source: dbSNP
start: 73395201
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73395203
feature_type: variation
id: rs1288330904
seq_region_name: 17
source: dbSNP
start: 73395201
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395203
feature_type: variation
id: rs765337277
seq_region_name: 17
source: dbSNP
start: 73395203
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395204
feature_type: variation
id: rs1287936221
seq_region_name: 17
source: dbSNP
start: 73395204
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395206
feature_type: variation
id: rs1451285697
seq_region_name: 17
source: dbSNP
start: 73395206
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395208
feature_type: variation
id: rs935838767
seq_region_name: 17
source: dbSNP
start: 73395208
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395209
feature_type: variation
id: rs757141765
seq_region_name: 17
source: dbSNP
start: 73395209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395210
feature_type: variation
id: rs759586319
seq_region_name: 17
source: dbSNP
start: 73395210
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395211
feature_type: variation
id: rs1482148891
seq_region_name: 17
source: dbSNP
start: 73395211
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395217
feature_type: variation
id: rs1181360717
seq_region_name: 17
source: dbSNP
start: 73395217
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395219
feature_type: variation
id: rs1028513588
seq_region_name: 17
source: dbSNP
start: 73395219
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395222
feature_type: variation
id: rs955715344
seq_region_name: 17
source: dbSNP
start: 73395222
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395223
feature_type: variation
id: rs1418494083
seq_region_name: 17
source: dbSNP
start: 73395223
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395225
feature_type: variation
id: rs1476033259
seq_region_name: 17
source: dbSNP
start: 73395225
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395227
feature_type: variation
id: rs376469000
seq_region_name: 17
source: dbSNP
start: 73395227
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395228
feature_type: variation
id: rs529292037
seq_region_name: 17
source: dbSNP
start: 73395228
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73395230
feature_type: variation
id: rs752822717
seq_region_name: 17
source: dbSNP
start: 73395230
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395231
feature_type: variation
id: rs1410151090
seq_region_name: 17
source: dbSNP
start: 73395231
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73395232
feature_type: variation
id: rs145582973
seq_region_name: 17
source: dbSNP
start: 73395232
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395233
feature_type: variation
id: rs144170771
seq_region_name: 17
source: dbSNP
start: 73395233
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395237
feature_type: variation
id: rs754206428
seq_region_name: 17
source: dbSNP
start: 73395237
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395238
feature_type: variation
id: rs1307887797
seq_region_name: 17
source: dbSNP
start: 73395238
strand: 1
-
alleles:
- CCACTCCTCCAGGTCCTCGATGGTGTAGTCCC
- CCACTCCTCCAGGTCCTCGATGGTGTAGTCCCACTCCTCCAGGTCCTCGATGGTGTAGTCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_insertion
end: 73395274
feature_type: variation
id: rs747393799
seq_region_name: 17
source: dbSNP
start: 73395243
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395245
feature_type: variation
id: rs2062961242
seq_region_name: 17
source: dbSNP
start: 73395245
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395246
feature_type: variation
id: rs1450588956
seq_region_name: 17
source: dbSNP
start: 73395246
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73395248
feature_type: variation
id: rs2062961294
seq_region_name: 17
source: dbSNP
start: 73395248
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395251
feature_type: variation
id: rs1282759519
seq_region_name: 17
source: dbSNP
start: 73395251
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395252
feature_type: variation
id: rs369708428
seq_region_name: 17
source: dbSNP
start: 73395252
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395255
feature_type: variation
id: rs779344771
seq_region_name: 17
source: dbSNP
start: 73395255
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73395260
feature_type: variation
id: rs749923803
seq_region_name: 17
source: dbSNP
start: 73395260
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395261
feature_type: variation
id: rs779642580
seq_region_name: 17
source: dbSNP
start: 73395261
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395262
feature_type: variation
id: rs1204543425
seq_region_name: 17
source: dbSNP
start: 73395262
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395263
feature_type: variation
id: rs779502040
seq_region_name: 17
source: dbSNP
start: 73395263
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395265
feature_type: variation
id: rs1380641573
seq_region_name: 17
source: dbSNP
start: 73395265
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395267
feature_type: variation
id: rs2062961558
seq_region_name: 17
source: dbSNP
start: 73395267
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395268
feature_type: variation
id: rs2062961591
seq_region_name: 17
source: dbSNP
start: 73395268
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395270
feature_type: variation
id: rs2145508207
seq_region_name: 17
source: dbSNP
start: 73395270
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395274
feature_type: variation
id: rs532844809
seq_region_name: 17
source: dbSNP
start: 73395274
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395275
feature_type: variation
id: rs974050104
seq_region_name: 17
source: dbSNP
start: 73395275
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395276
feature_type: variation
id: rs1396495609
seq_region_name: 17
source: dbSNP
start: 73395276
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395278
feature_type: variation
id: rs781133747
seq_region_name: 17
source: dbSNP
start: 73395278
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395279
feature_type: variation
id: rs975289219
seq_region_name: 17
source: dbSNP
start: 73395279
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395281
feature_type: variation
id: rs748016312
seq_region_name: 17
source: dbSNP
start: 73395281
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395282
feature_type: variation
id: rs933814638
seq_region_name: 17
source: dbSNP
start: 73395282
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395283
feature_type: variation
id: rs919894226
seq_region_name: 17
source: dbSNP
start: 73395283
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395284
feature_type: variation
id: rs138801054
seq_region_name: 17
source: dbSNP
start: 73395284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395293
feature_type: variation
id: rs1473325223
seq_region_name: 17
source: dbSNP
start: 73395293
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395295
feature_type: variation
id: rs2062961921
seq_region_name: 17
source: dbSNP
start: 73395295
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73395296
feature_type: variation
id: rs148937818
seq_region_name: 17
source: dbSNP
start: 73395296
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395297
feature_type: variation
id: rs559909325
seq_region_name: 17
source: dbSNP
start: 73395297
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395300
feature_type: variation
id: rs1444144953
seq_region_name: 17
source: dbSNP
start: 73395300
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395306
feature_type: variation
id: rs775653984
seq_region_name: 17
source: dbSNP
start: 73395306
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395307
feature_type: variation
id: rs760819239
seq_region_name: 17
source: dbSNP
start: 73395307
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395313
feature_type: variation
id: rs764366177
seq_region_name: 17
source: dbSNP
start: 73395313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395314
feature_type: variation
id: rs754186093
seq_region_name: 17
source: dbSNP
start: 73395314
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395320
feature_type: variation
id: rs1332839827
seq_region_name: 17
source: dbSNP
start: 73395320
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395321
feature_type: variation
id: rs373852406
seq_region_name: 17
source: dbSNP
start: 73395321
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395324
feature_type: variation
id: rs765740285
seq_region_name: 17
source: dbSNP
start: 73395324
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395328
feature_type: variation
id: rs201041336
seq_region_name: 17
source: dbSNP
start: 73395328
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395329
feature_type: variation
id: rs143702793
seq_region_name: 17
source: dbSNP
start: 73395329
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73395333
feature_type: variation
id: rs779369281
seq_region_name: 17
source: dbSNP
start: 73395333
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395334
feature_type: variation
id: rs1599521109
seq_region_name: 17
source: dbSNP
start: 73395334
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73395341
feature_type: variation
id: rs755308806
seq_region_name: 17
source: dbSNP
start: 73395341
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73395342
feature_type: variation
id: rs751184995
seq_region_name: 17
source: dbSNP
start: 73395342
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395345
feature_type: variation
id: rs754667962
seq_region_name: 17
source: dbSNP
start: 73395345
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395346
feature_type: variation
id: rs2062962432
seq_region_name: 17
source: dbSNP
start: 73395346
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395349
feature_type: variation
id: rs2062962456
seq_region_name: 17
source: dbSNP
start: 73395349
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395350
feature_type: variation
id: rs1277912011
seq_region_name: 17
source: dbSNP
start: 73395350
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73395353
feature_type: variation
id: rs1356743829
seq_region_name: 17
source: dbSNP
start: 73395353
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395354
feature_type: variation
id: rs781043454
seq_region_name: 17
source: dbSNP
start: 73395354
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395357
feature_type: variation
id: rs747923746
seq_region_name: 17
source: dbSNP
start: 73395357
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395361
feature_type: variation
id: rs2062962609
seq_region_name: 17
source: dbSNP
start: 73395361
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395363
feature_type: variation
id: rs1245764919
seq_region_name: 17
source: dbSNP
start: 73395363
strand: 1
-
alleles:
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- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1216667006
seq_region_name: 17
source: dbSNP
start: 73395364
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1339961193
seq_region_name: 17
source: dbSNP
start: 73395366
strand: 1
-
alleles:
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- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1599521152
seq_region_name: 17
source: dbSNP
start: 73395369
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395370
feature_type: variation
id: rs1448471859
seq_region_name: 17
source: dbSNP
start: 73395370
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1193930649
seq_region_name: 17
source: dbSNP
start: 73395375
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395378
feature_type: variation
id: rs891554719
seq_region_name: 17
source: dbSNP
start: 73395378
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395380
feature_type: variation
id: rs1396348802
seq_region_name: 17
source: dbSNP
start: 73395380
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs1476796799
seq_region_name: 17
source: dbSNP
start: 73395382
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73395383
feature_type: variation
id: rs2062962883
seq_region_name: 17
source: dbSNP
start: 73395383
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73395384
feature_type: variation
id: rs769438071
seq_region_name: 17
source: dbSNP
start: 73395384
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395385
feature_type: variation
id: rs200100217
seq_region_name: 17
source: dbSNP
start: 73395385
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395386
feature_type: variation
id: rs1401602435
seq_region_name: 17
source: dbSNP
start: 73395386
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs2062963009
seq_region_name: 17
source: dbSNP
start: 73395387
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395390
feature_type: variation
id: rs1306079015
seq_region_name: 17
source: dbSNP
start: 73395390
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73395392
feature_type: variation
id: rs749122671
seq_region_name: 17
source: dbSNP
start: 73395392
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395396
feature_type: variation
id: rs1599521206
seq_region_name: 17
source: dbSNP
start: 73395396
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395397
feature_type: variation
id: rs1599521210
seq_region_name: 17
source: dbSNP
start: 73395397
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395398
feature_type: variation
id: rs375496820
seq_region_name: 17
source: dbSNP
start: 73395398
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395399
feature_type: variation
id: rs202081833
seq_region_name: 17
source: dbSNP
start: 73395399
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73395400
feature_type: variation
id: rs186203685
seq_region_name: 17
source: dbSNP
start: 73395400
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73395401
feature_type: variation
id: rs768842560
seq_region_name: 17
source: dbSNP
start: 73395401
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73395402
feature_type: variation
id: rs1166687520
seq_region_name: 17
source: dbSNP
start: 73395402
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73395403
feature_type: variation
id: rs878870980
seq_region_name: 17
source: dbSNP
start: 73395403
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73395404
feature_type: variation
id: rs2062963302
seq_region_name: 17
source: dbSNP
start: 73395404
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73395405
feature_type: variation
id: rs191130003
seq_region_name: 17
source: dbSNP
start: 73395405
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73395409
feature_type: variation
id: rs1351336828
seq_region_name: 17
source: dbSNP
start: 73395409
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395410
feature_type: variation
id: rs1599521257
seq_region_name: 17
source: dbSNP
start: 73395410
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395413
feature_type: variation
id: rs975093609
seq_region_name: 17
source: dbSNP
start: 73395413
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs762051723
seq_region_name: 17
source: dbSNP
start: 73395416
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395417
feature_type: variation
id: rs900147010
seq_region_name: 17
source: dbSNP
start: 73395417
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395418
feature_type: variation
id: rs539953066
seq_region_name: 17
source: dbSNP
start: 73395418
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395420
feature_type: variation
id: rs1464320731
seq_region_name: 17
source: dbSNP
start: 73395420
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395424
feature_type: variation
id: rs997136073
seq_region_name: 17
source: dbSNP
start: 73395424
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395425
feature_type: variation
id: rs370737930
seq_region_name: 17
source: dbSNP
start: 73395425
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395429
feature_type: variation
id: rs369555374
seq_region_name: 17
source: dbSNP
start: 73395429
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395432
feature_type: variation
id: rs1291684841
seq_region_name: 17
source: dbSNP
start: 73395432
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395433
feature_type: variation
id: rs763368278
seq_region_name: 17
source: dbSNP
start: 73395433
strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395438
feature_type: variation
id: rs1197579998
seq_region_name: 17
source: dbSNP
start: 73395433
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395434
feature_type: variation
id: rs2062963659
seq_region_name: 17
source: dbSNP
start: 73395434
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395437
feature_type: variation
id: rs1470779220
seq_region_name: 17
source: dbSNP
start: 73395437
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395438
feature_type: variation
id: rs2062963704
seq_region_name: 17
source: dbSNP
start: 73395438
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395442
feature_type: variation
id: rs766972117
seq_region_name: 17
source: dbSNP
start: 73395442
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395444
feature_type: variation
id: rs2062963738
seq_region_name: 17
source: dbSNP
start: 73395444
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395449
feature_type: variation
id: rs1258622508
seq_region_name: 17
source: dbSNP
start: 73395449
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395457
feature_type: variation
id: rs2062963778
seq_region_name: 17
source: dbSNP
start: 73395457
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395462
feature_type: variation
id: rs986768363
seq_region_name: 17
source: dbSNP
start: 73395462
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395468
feature_type: variation
id: rs2062963825
seq_region_name: 17
source: dbSNP
start: 73395468
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395469
feature_type: variation
id: rs1328823487
seq_region_name: 17
source: dbSNP
start: 73395469
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395470
feature_type: variation
id: rs2062963875
seq_region_name: 17
source: dbSNP
start: 73395470
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395473
feature_type: variation
id: rs908367392
seq_region_name: 17
source: dbSNP
start: 73395473
strand: 1
-
alleles:
- CCAGGGCGCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395484
feature_type: variation
id: rs2145508890
seq_region_name: 17
source: dbSNP
start: 73395475
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395478
feature_type: variation
id: rs573157332
seq_region_name: 17
source: dbSNP
start: 73395478
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395479
feature_type: variation
id: rs1599521338
seq_region_name: 17
source: dbSNP
start: 73395479
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395480
feature_type: variation
id: rs1599521341
seq_region_name: 17
source: dbSNP
start: 73395480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395481
feature_type: variation
id: rs755509014
seq_region_name: 17
source: dbSNP
start: 73395481
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395482
feature_type: variation
id: rs1038382391
seq_region_name: 17
source: dbSNP
start: 73395482
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395483
feature_type: variation
id: rs2062964011
seq_region_name: 17
source: dbSNP
start: 73395483
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395484
feature_type: variation
id: rs1437396491
seq_region_name: 17
source: dbSNP
start: 73395484
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395491
feature_type: variation
id: rs1333193262
seq_region_name: 17
source: dbSNP
start: 73395491
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395492
feature_type: variation
id: rs2062964069
seq_region_name: 17
source: dbSNP
start: 73395492
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395497
feature_type: variation
id: rs9894473
seq_region_name: 17
source: dbSNP
start: 73395497
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395500
feature_type: variation
id: rs2062964088
seq_region_name: 17
source: dbSNP
start: 73395500
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395505
feature_type: variation
id: rs559614973
seq_region_name: 17
source: dbSNP
start: 73395505
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395507
feature_type: variation
id: rs1446487435
seq_region_name: 17
source: dbSNP
start: 73395507
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395510
feature_type: variation
id: rs2062964157
seq_region_name: 17
source: dbSNP
start: 73395510
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395512
feature_type: variation
id: rs961453448
seq_region_name: 17
source: dbSNP
start: 73395512
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395513
feature_type: variation
id: rs948700879
seq_region_name: 17
source: dbSNP
start: 73395513
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395517
feature_type: variation
id: rs2062964233
seq_region_name: 17
source: dbSNP
start: 73395517
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395522
feature_type: variation
id: rs1044776076
seq_region_name: 17
source: dbSNP
start: 73395522
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395523
feature_type: variation
id: rs2062964284
seq_region_name: 17
source: dbSNP
start: 73395522
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395526
feature_type: variation
id: rs2062964309
seq_region_name: 17
source: dbSNP
start: 73395526
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395530
feature_type: variation
id: rs2062964332
seq_region_name: 17
source: dbSNP
start: 73395530
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395532
feature_type: variation
id: rs1466759890
seq_region_name: 17
source: dbSNP
start: 73395532
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395540
feature_type: variation
id: rs1599521392
seq_region_name: 17
source: dbSNP
start: 73395540
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395541
feature_type: variation
id: rs1599521396
seq_region_name: 17
source: dbSNP
start: 73395541
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395542
feature_type: variation
id: rs1251217995
seq_region_name: 17
source: dbSNP
start: 73395542
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395543
feature_type: variation
id: rs1420342878
seq_region_name: 17
source: dbSNP
start: 73395543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395545
feature_type: variation
id: rs907231714
seq_region_name: 17
source: dbSNP
start: 73395545
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395550
feature_type: variation
id: rs1003528761
seq_region_name: 17
source: dbSNP
start: 73395550
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395556
feature_type: variation
id: rs1053412300
seq_region_name: 17
source: dbSNP
start: 73395556
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395557
feature_type: variation
id: rs748848859
seq_region_name: 17
source: dbSNP
start: 73395557
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395559
feature_type: variation
id: rs970452101
seq_region_name: 17
source: dbSNP
start: 73395559
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395565
feature_type: variation
id: rs2062964551
seq_region_name: 17
source: dbSNP
start: 73395565
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395570
feature_type: variation
id: rs1457138007
seq_region_name: 17
source: dbSNP
start: 73395566
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73395701
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73395705
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73395707
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73395711
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73395711
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395713
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395714
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395716
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395721
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73395724
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395731
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395733
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73395734
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73395739
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73395740
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs980247793
seq_region_name: 17
source: dbSNP
start: 73395741
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395741
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395742
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395744
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395747
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73395753
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395754
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395753
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062966473
seq_region_name: 17
source: dbSNP
start: 73395755
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395760
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id: rs2062966498
seq_region_name: 17
source: dbSNP
start: 73395760
strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73395824
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395828
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73395841
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395846
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395847
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1421382461
seq_region_name: 17
source: dbSNP
start: 73395857
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73395868
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395872
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395874
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73395881
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395882
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395885
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395886
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395888
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395903
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395905
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395907
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062967562
seq_region_name: 17
source: dbSNP
start: 73395908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs569494139
seq_region_name: 17
source: dbSNP
start: 73395911
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395913
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1316668985
seq_region_name: 17
source: dbSNP
start: 73395918
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395919
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73395920
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062967714
seq_region_name: 17
source: dbSNP
start: 73395921
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062967727
seq_region_name: 17
source: dbSNP
start: 73395921
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1028073362
seq_region_name: 17
source: dbSNP
start: 73395922
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs371190241
seq_region_name: 17
source: dbSNP
start: 73395923
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395927
feature_type: variation
id: rs1175880118
seq_region_name: 17
source: dbSNP
start: 73395927
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395938
feature_type: variation
id: rs2062967891
seq_region_name: 17
source: dbSNP
start: 73395938
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395948
feature_type: variation
id: rs1599521844
seq_region_name: 17
source: dbSNP
start: 73395948
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs142765833
seq_region_name: 17
source: dbSNP
start: 73395949
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062967963
seq_region_name: 17
source: dbSNP
start: 73395953
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395959
feature_type: variation
id: rs2062967989
seq_region_name: 17
source: dbSNP
start: 73395954
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395956
feature_type: variation
id: rs978574539
seq_region_name: 17
source: dbSNP
start: 73395956
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1169837851
seq_region_name: 17
source: dbSNP
start: 73395960
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062968040
seq_region_name: 17
source: dbSNP
start: 73395967
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395971
feature_type: variation
id: rs1466237600
seq_region_name: 17
source: dbSNP
start: 73395971
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395973
feature_type: variation
id: rs2062968058
seq_region_name: 17
source: dbSNP
start: 73395973
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395975
feature_type: variation
id: rs2062968077
seq_region_name: 17
source: dbSNP
start: 73395975
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395976
feature_type: variation
id: rs36119795
seq_region_name: 17
source: dbSNP
start: 73395975
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395977
feature_type: variation
id: rs1599521868
seq_region_name: 17
source: dbSNP
start: 73395977
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395978
feature_type: variation
id: rs773242475
seq_region_name: 17
source: dbSNP
start: 73395978
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395986
feature_type: variation
id: rs1463926097
seq_region_name: 17
source: dbSNP
start: 73395986
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395994
feature_type: variation
id: rs1374816972
seq_region_name: 17
source: dbSNP
start: 73395994
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395996
feature_type: variation
id: rs2062968185
seq_region_name: 17
source: dbSNP
start: 73395996
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395997
feature_type: variation
id: rs921677763
seq_region_name: 17
source: dbSNP
start: 73395997
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395998
feature_type: variation
id: rs2062968230
seq_region_name: 17
source: dbSNP
start: 73395998
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73395999
feature_type: variation
id: rs2145510035
seq_region_name: 17
source: dbSNP
start: 73395999
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396001
feature_type: variation
id: rs71380174
seq_region_name: 17
source: dbSNP
start: 73396001
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396005
feature_type: variation
id: rs931714597
seq_region_name: 17
source: dbSNP
start: 73396005
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396012
feature_type: variation
id: rs1015440914
seq_region_name: 17
source: dbSNP
start: 73396012
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396013
feature_type: variation
id: rs2062968318
seq_region_name: 17
source: dbSNP
start: 73396013
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396015
feature_type: variation
id: rs1568381056
seq_region_name: 17
source: dbSNP
start: 73396015
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396016
feature_type: variation
id: rs2145510075
seq_region_name: 17
source: dbSNP
start: 73396016
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396019
feature_type: variation
id: rs2062968354
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396178
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73396179
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73396182
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396186
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396189
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396190
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73396200
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396201
strand: 1
-
alleles:
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- AGAAAAG
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396201
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396202
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396203
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396219
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396221
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396222
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396223
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062969829
seq_region_name: 17
source: dbSNP
start: 73396227
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396228
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062969871
seq_region_name: 17
source: dbSNP
start: 73396237
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396245
feature_type: variation
id: rs1008418983
seq_region_name: 17
source: dbSNP
start: 73396245
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs987221078
seq_region_name: 17
source: dbSNP
start: 73396250
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396251
feature_type: variation
id: rs368062265
seq_region_name: 17
source: dbSNP
start: 73396251
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73396256
feature_type: variation
id: rs150587283
seq_region_name: 17
source: dbSNP
start: 73396255
strand: 1
-
alleles:
- C
- A
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73396472
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73396475
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396478
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396483
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396485
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396488
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1036783225
seq_region_name: 17
source: dbSNP
start: 73396489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396490
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396491
strand: 1
-
alleles:
- CCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396497
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396498
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1463624100
seq_region_name: 17
source: dbSNP
start: 73396500
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73396501
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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end: 73396504
feature_type: variation
id: rs2062971999
seq_region_name: 17
source: dbSNP
start: 73396504
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062972023
seq_region_name: 17
source: dbSNP
start: 73396506
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs961733939
seq_region_name: 17
source: dbSNP
start: 73396508
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396719
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73396724
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73396725
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396727
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73396729
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396731
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396734
strand: 1
-
alleles:
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- TG
assembly_name: GRCh38
clinical_significance: []
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end: 73396735
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seq_region_name: 17
source: dbSNP
start: 73396734
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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start: 73396910
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396920
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73396928
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396929
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73396935
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73396939
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396941
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396946
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73396947
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396948
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396951
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396951
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396953
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73396956
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs931056038
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397102
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73397103
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397104
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397105
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397108
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397113
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397114
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397118
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397120
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062977569
seq_region_name: 17
source: dbSNP
start: 73397122
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397138
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062977719
seq_region_name: 17
source: dbSNP
start: 73397139
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1280865083
seq_region_name: 17
source: dbSNP
start: 73397146
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397153
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1374639402
seq_region_name: 17
source: dbSNP
start: 73397154
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397161
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397173
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145512952
seq_region_name: 17
source: dbSNP
start: 73397174
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397178
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062977898
seq_region_name: 17
source: dbSNP
start: 73397186
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397187
feature_type: variation
id: rs527857136
seq_region_name: 17
source: dbSNP
start: 73397187
strand: 1
-
alleles:
- T
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clinical_significance: []
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73397288
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73397293
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397300
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397308
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397310
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73397312
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397315
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397320
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397323
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397324
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397325
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1486832820
seq_region_name: 17
source: dbSNP
start: 73397328
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs897867974
seq_region_name: 17
source: dbSNP
start: 73397333
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73397334
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397338
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062979303
seq_region_name: 17
source: dbSNP
start: 73397339
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs34245002
seq_region_name: 17
source: dbSNP
start: 73397343
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1027868488
seq_region_name: 17
source: dbSNP
start: 73397345
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs547346767
seq_region_name: 17
source: dbSNP
start: 73397346
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs952183443
seq_region_name: 17
source: dbSNP
start: 73397348
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062979441
seq_region_name: 17
source: dbSNP
start: 73397353
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs967584652
seq_region_name: 17
source: dbSNP
start: 73397358
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062979465
seq_region_name: 17
source: dbSNP
start: 73397367
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73397368
feature_type: variation
id: rs1384253727
seq_region_name: 17
source: dbSNP
start: 73397368
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs977626843
seq_region_name: 17
source: dbSNP
start: 73397369
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397374
feature_type: variation
id: rs2062979534
seq_region_name: 17
source: dbSNP
start: 73397369
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1325776917
seq_region_name: 17
source: dbSNP
start: 73397370
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565869679
seq_region_name: 17
source: dbSNP
start: 73397378
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062979606
seq_region_name: 17
source: dbSNP
start: 73397380
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73397383
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs986604974
seq_region_name: 17
source: dbSNP
start: 73397384
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062979680
seq_region_name: 17
source: dbSNP
start: 73397386
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145513588
seq_region_name: 17
source: dbSNP
start: 73397389
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397395
feature_type: variation
id: rs2062979702
seq_region_name: 17
source: dbSNP
start: 73397395
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397399
feature_type: variation
id: rs867697604
seq_region_name: 17
source: dbSNP
start: 73397399
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062979748
seq_region_name: 17
source: dbSNP
start: 73397400
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397401
feature_type: variation
id: rs2062979767
seq_region_name: 17
source: dbSNP
start: 73397401
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397410
feature_type: variation
id: rs2062979785
seq_region_name: 17
source: dbSNP
start: 73397410
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397411
feature_type: variation
id: rs1175214874
seq_region_name: 17
source: dbSNP
start: 73397411
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397412
feature_type: variation
id: rs2062979844
seq_region_name: 17
source: dbSNP
start: 73397412
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397416
feature_type: variation
id: rs554743799
seq_region_name: 17
source: dbSNP
start: 73397416
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397419
feature_type: variation
id: rs118158762
seq_region_name: 17
source: dbSNP
start: 73397419
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73397601
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73397604
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397608
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397615
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397620
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397621
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73397622
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73397623
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2062982425
seq_region_name: 17
source: dbSNP
start: 73397624
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397629
feature_type: variation
id: rs2062982446
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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seq_region_name: 17
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397891
feature_type: variation
id: rs2062984847
seq_region_name: 17
source: dbSNP
start: 73397889
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs998636490
seq_region_name: 17
source: dbSNP
start: 73397890
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062984887
seq_region_name: 17
source: dbSNP
start: 73397894
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397897
feature_type: variation
id: rs548385090
seq_region_name: 17
source: dbSNP
start: 73397897
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397898
feature_type: variation
id: rs569802754
seq_region_name: 17
source: dbSNP
start: 73397898
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397900
feature_type: variation
id: rs1599523767
seq_region_name: 17
source: dbSNP
start: 73397900
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397907
feature_type: variation
id: rs2062984954
seq_region_name: 17
source: dbSNP
start: 73397907
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397908
feature_type: variation
id: rs1454272905
seq_region_name: 17
source: dbSNP
start: 73397908
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397911
feature_type: variation
id: rs2062985000
seq_region_name: 17
source: dbSNP
start: 73397911
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397912
feature_type: variation
id: rs376888468
seq_region_name: 17
source: dbSNP
start: 73397912
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397914
feature_type: variation
id: rs2062985060
seq_region_name: 17
source: dbSNP
start: 73397914
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397915
feature_type: variation
id: rs537159252
seq_region_name: 17
source: dbSNP
start: 73397915
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397922
feature_type: variation
id: rs772044784
seq_region_name: 17
source: dbSNP
start: 73397922
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397927
feature_type: variation
id: rs7224026
seq_region_name: 17
source: dbSNP
start: 73397927
strand: 1
-
alleles:
- AGAAAGA
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397934
feature_type: variation
id: rs1249270496
seq_region_name: 17
source: dbSNP
start: 73397928
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397929
feature_type: variation
id: rs2062985230
seq_region_name: 17
source: dbSNP
start: 73397929
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397930
feature_type: variation
id: rs2062985254
seq_region_name: 17
source: dbSNP
start: 73397930
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397931
feature_type: variation
id: rs2062985277
seq_region_name: 17
source: dbSNP
start: 73397931
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397932
feature_type: variation
id: rs2062985297
seq_region_name: 17
source: dbSNP
start: 73397932
strand: 1
-
alleles:
- AGAGAG
- AGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397937
feature_type: variation
id: rs1203313393
seq_region_name: 17
source: dbSNP
start: 73397932
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397933
feature_type: variation
id: rs966245135
seq_region_name: 17
source: dbSNP
start: 73397933
strand: 1
-
alleles:
- A
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397936
feature_type: variation
id: rs2062985373
seq_region_name: 17
source: dbSNP
start: 73397936
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397941
feature_type: variation
id: rs1307705935
seq_region_name: 17
source: dbSNP
start: 73397941
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397946
feature_type: variation
id: rs2062985433
seq_region_name: 17
source: dbSNP
start: 73397946
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397949
feature_type: variation
id: rs1276596608
seq_region_name: 17
source: dbSNP
start: 73397949
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397950
feature_type: variation
id: rs975867474
seq_region_name: 17
source: dbSNP
start: 73397950
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397951
feature_type: variation
id: rs1713440146
seq_region_name: 17
source: dbSNP
start: 73397951
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397960
feature_type: variation
id: rs777600620
seq_region_name: 17
source: dbSNP
start: 73397960
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397962
feature_type: variation
id: rs2062985530
seq_region_name: 17
source: dbSNP
start: 73397962
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397963
feature_type: variation
id: rs1379742364
seq_region_name: 17
source: dbSNP
start: 73397963
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397965
feature_type: variation
id: rs2062985560
seq_region_name: 17
source: dbSNP
start: 73397965
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397968
feature_type: variation
id: rs919121021
seq_region_name: 17
source: dbSNP
start: 73397968
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397973
feature_type: variation
id: rs929384992
seq_region_name: 17
source: dbSNP
start: 73397973
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397974
feature_type: variation
id: rs1371190876
seq_region_name: 17
source: dbSNP
start: 73397974
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397977
feature_type: variation
id: rs1297834527
seq_region_name: 17
source: dbSNP
start: 73397977
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397978
feature_type: variation
id: rs1443275287
seq_region_name: 17
source: dbSNP
start: 73397978
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397983
feature_type: variation
id: rs187740645
seq_region_name: 17
source: dbSNP
start: 73397983
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397984
feature_type: variation
id: rs374187616
seq_region_name: 17
source: dbSNP
start: 73397984
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397985
feature_type: variation
id: rs1410192097
seq_region_name: 17
source: dbSNP
start: 73397985
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397988
feature_type: variation
id: rs1568381927
seq_region_name: 17
source: dbSNP
start: 73397988
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397989
feature_type: variation
id: rs368063500
seq_region_name: 17
source: dbSNP
start: 73397989
strand: 1
-
alleles:
- AGA
- AGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397991
feature_type: variation
id: rs781542285
seq_region_name: 17
source: dbSNP
start: 73397989
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397996
feature_type: variation
id: rs1326750480
seq_region_name: 17
source: dbSNP
start: 73397996
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397998
feature_type: variation
id: rs77540605
seq_region_name: 17
source: dbSNP
start: 73397998
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73397999
feature_type: variation
id: rs1385102731
seq_region_name: 17
source: dbSNP
start: 73397999
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398000
feature_type: variation
id: rs767168014
seq_region_name: 17
source: dbSNP
start: 73398000
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398002
feature_type: variation
id: rs112870762
seq_region_name: 17
source: dbSNP
start: 73398002
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398006
feature_type: variation
id: rs7209509
seq_region_name: 17
source: dbSNP
start: 73398006
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398009
feature_type: variation
id: rs2062985945
seq_region_name: 17
source: dbSNP
start: 73398009
strand: 1
-
alleles:
- CAC
- CACAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398011
feature_type: variation
id: rs2062985969
seq_region_name: 17
source: dbSNP
start: 73398009
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398010
feature_type: variation
id: rs1599523917
seq_region_name: 17
source: dbSNP
start: 73398010
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398011
feature_type: variation
id: rs777365139
seq_region_name: 17
source: dbSNP
start: 73398011
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398012
feature_type: variation
id: rs1328152205
seq_region_name: 17
source: dbSNP
start: 73398012
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398016
feature_type: variation
id: rs749173913
seq_region_name: 17
source: dbSNP
start: 73398016
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398021
feature_type: variation
id: rs375099752
seq_region_name: 17
source: dbSNP
start: 73398021
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398022
feature_type: variation
id: rs369129277
seq_region_name: 17
source: dbSNP
start: 73398022
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398025
feature_type: variation
id: rs2062986155
seq_region_name: 17
source: dbSNP
start: 73398026
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398026
feature_type: variation
id: rs1208910147
seq_region_name: 17
source: dbSNP
start: 73398026
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398027
feature_type: variation
id: rs1250585220
seq_region_name: 17
source: dbSNP
start: 73398027
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398028
feature_type: variation
id: rs1483781445
seq_region_name: 17
source: dbSNP
start: 73398028
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73398029
feature_type: variation
id: rs778869325
seq_region_name: 17
source: dbSNP
start: 73398029
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73398033
feature_type: variation
id: rs1599523969
seq_region_name: 17
source: dbSNP
start: 73398033
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398036
feature_type: variation
id: rs2062986299
seq_region_name: 17
source: dbSNP
start: 73398036
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398037
feature_type: variation
id: rs2062986324
seq_region_name: 17
source: dbSNP
start: 73398037
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398038
feature_type: variation
id: rs2062986362
seq_region_name: 17
source: dbSNP
start: 73398038
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398041
feature_type: variation
id: rs2062986391
seq_region_name: 17
source: dbSNP
start: 73398041
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398042
feature_type: variation
id: rs747059860
seq_region_name: 17
source: dbSNP
start: 73398042
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398043
feature_type: variation
id: rs1472434982
seq_region_name: 17
source: dbSNP
start: 73398043
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398044
feature_type: variation
id: rs768679122
seq_region_name: 17
source: dbSNP
start: 73398044
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398046
feature_type: variation
id: rs2062986495
seq_region_name: 17
source: dbSNP
start: 73398046
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398047
feature_type: variation
id: rs776711911
seq_region_name: 17
source: dbSNP
start: 73398047
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398050
feature_type: variation
id: rs748256871
seq_region_name: 17
source: dbSNP
start: 73398050
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398051
feature_type: variation
id: rs770056125
seq_region_name: 17
source: dbSNP
start: 73398051
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398053
feature_type: variation
id: rs773439470
seq_region_name: 17
source: dbSNP
start: 73398053
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398055
feature_type: variation
id: rs1411747558
seq_region_name: 17
source: dbSNP
start: 73398055
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398056
feature_type: variation
id: rs1306050574
seq_region_name: 17
source: dbSNP
start: 73398056
strand: 1
-
alleles:
- GTCTCACTG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73398065
feature_type: variation
id: rs1377778879
seq_region_name: 17
source: dbSNP
start: 73398057
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398058
feature_type: variation
id: rs1349824086
seq_region_name: 17
source: dbSNP
start: 73398058
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398067
feature_type: variation
id: rs1435595299
seq_region_name: 17
source: dbSNP
start: 73398067
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398068
feature_type: variation
id: rs1315042886
seq_region_name: 17
source: dbSNP
start: 73398068
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398069
feature_type: variation
id: rs1026352563
seq_region_name: 17
source: dbSNP
start: 73398069
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398072
feature_type: variation
id: rs542845961
seq_region_name: 17
source: dbSNP
start: 73398072
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398073
feature_type: variation
id: rs766963724
seq_region_name: 17
source: dbSNP
start: 73398073
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398076
feature_type: variation
id: rs2145515528
seq_region_name: 17
source: dbSNP
start: 73398076
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398080
feature_type: variation
id: rs561159742
seq_region_name: 17
source: dbSNP
start: 73398080
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398082
feature_type: variation
id: rs2062986882
seq_region_name: 17
source: dbSNP
start: 73398082
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398083
feature_type: variation
id: rs767080162
seq_region_name: 17
source: dbSNP
start: 73398083
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398087
feature_type: variation
id: rs1251594219
seq_region_name: 17
source: dbSNP
start: 73398087
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398095
feature_type: variation
id: rs1599524091
seq_region_name: 17
source: dbSNP
start: 73398095
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398096
feature_type: variation
id: rs371361224
seq_region_name: 17
source: dbSNP
start: 73398096
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398097
feature_type: variation
id: rs375439400
seq_region_name: 17
source: dbSNP
start: 73398097
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73398098
feature_type: variation
id: rs748271451
seq_region_name: 17
source: dbSNP
start: 73398098
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398100
feature_type: variation
id: rs1414582160
seq_region_name: 17
source: dbSNP
start: 73398100
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398102
feature_type: variation
id: rs1202423995
seq_region_name: 17
source: dbSNP
start: 73398102
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398103
feature_type: variation
id: rs1599524131
seq_region_name: 17
source: dbSNP
start: 73398103
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398104
feature_type: variation
id: rs1183278820
seq_region_name: 17
source: dbSNP
start: 73398104
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398105
feature_type: variation
id: rs755716815
seq_region_name: 17
source: dbSNP
start: 73398105
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398106
feature_type: variation
id: rs2062987200
seq_region_name: 17
source: dbSNP
start: 73398106
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398107
feature_type: variation
id: rs1483032583
seq_region_name: 17
source: dbSNP
start: 73398107
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398109
feature_type: variation
id: rs2145515691
seq_region_name: 17
source: dbSNP
start: 73398109
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73398112
feature_type: variation
id: rs763865216
seq_region_name: 17
source: dbSNP
start: 73398112
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398116
feature_type: variation
id: rs753552394
seq_region_name: 17
source: dbSNP
start: 73398116
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398125
feature_type: variation
id: rs1360194423
seq_region_name: 17
source: dbSNP
start: 73398125
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398127
feature_type: variation
id: rs2062987359
seq_region_name: 17
source: dbSNP
start: 73398127
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398131
feature_type: variation
id: rs2062987390
seq_region_name: 17
source: dbSNP
start: 73398131
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398133
feature_type: variation
id: rs757114784
seq_region_name: 17
source: dbSNP
start: 73398133
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398137
feature_type: variation
id: rs778707866
seq_region_name: 17
source: dbSNP
start: 73398137
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398140
feature_type: variation
id: rs2145515764
seq_region_name: 17
source: dbSNP
start: 73398140
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398141
feature_type: variation
id: rs745754736
seq_region_name: 17
source: dbSNP
start: 73398141
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398143
feature_type: variation
id: rs758340614
seq_region_name: 17
source: dbSNP
start: 73398143
strand: 1
-
alleles:
- GGGGGGG
- GGGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73398149
feature_type: variation
id: rs769945438
seq_region_name: 17
source: dbSNP
start: 73398143
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398144
feature_type: variation
id: rs1370076502
seq_region_name: 17
source: dbSNP
start: 73398144
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398145
feature_type: variation
id: rs1032768155
seq_region_name: 17
source: dbSNP
start: 73398145
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398148
feature_type: variation
id: rs748321283
seq_region_name: 17
source: dbSNP
start: 73398148
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398151
feature_type: variation
id: rs2145515884
seq_region_name: 17
source: dbSNP
start: 73398151
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398153
feature_type: variation
id: rs769889158
seq_region_name: 17
source: dbSNP
start: 73398153
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398155
feature_type: variation
id: rs1376690569
seq_region_name: 17
source: dbSNP
start: 73398155
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398156
feature_type: variation
id: rs1395238751
seq_region_name: 17
source: dbSNP
start: 73398156
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398157
feature_type: variation
id: rs1295773395
seq_region_name: 17
source: dbSNP
start: 73398157
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398158
feature_type: variation
id: rs2062987811
seq_region_name: 17
source: dbSNP
start: 73398158
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398160
feature_type: variation
id: rs959570258
seq_region_name: 17
source: dbSNP
start: 73398160
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398161
feature_type: variation
id: rs773525846
seq_region_name: 17
source: dbSNP
start: 73398161
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398162
feature_type: variation
id: rs749506739
seq_region_name: 17
source: dbSNP
start: 73398162
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398163
feature_type: variation
id: rs917787705
seq_region_name: 17
source: dbSNP
start: 73398163
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398164
feature_type: variation
id: rs1348053596
seq_region_name: 17
source: dbSNP
start: 73398164
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398170
feature_type: variation
id: rs1599524243
seq_region_name: 17
source: dbSNP
start: 73398170
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398174
feature_type: variation
id: rs747725916
seq_region_name: 17
source: dbSNP
start: 73398174
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398175
feature_type: variation
id: rs1258292112
seq_region_name: 17
source: dbSNP
start: 73398175
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398176
feature_type: variation
id: rs2062988097
seq_region_name: 17
source: dbSNP
start: 73398176
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398178
feature_type: variation
id: rs2062988124
seq_region_name: 17
source: dbSNP
start: 73398178
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398179
feature_type: variation
id: rs1482448347
seq_region_name: 17
source: dbSNP
start: 73398179
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398180
feature_type: variation
id: rs1200266176
seq_region_name: 17
source: dbSNP
start: 73398180
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398188
feature_type: variation
id: rs2062988210
seq_region_name: 17
source: dbSNP
start: 73398188
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398190
feature_type: variation
id: rs1248842041
seq_region_name: 17
source: dbSNP
start: 73398190
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398192
feature_type: variation
id: rs1599524277
seq_region_name: 17
source: dbSNP
start: 73398192
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398194
feature_type: variation
id: rs774871709
seq_region_name: 17
source: dbSNP
start: 73398194
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398197
feature_type: variation
id: rs1201956419
seq_region_name: 17
source: dbSNP
start: 73398194
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398196
feature_type: variation
id: rs1468503480
seq_region_name: 17
source: dbSNP
start: 73398196
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398197
feature_type: variation
id: rs760053808
seq_region_name: 17
source: dbSNP
start: 73398197
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398198
feature_type: variation
id: rs1216613817
seq_region_name: 17
source: dbSNP
start: 73398198
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398199
feature_type: variation
id: rs768206704
seq_region_name: 17
source: dbSNP
start: 73398199
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398207
feature_type: variation
id: rs1331269149
seq_region_name: 17
source: dbSNP
start: 73398207
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398210
feature_type: variation
id: rs1291668945
seq_region_name: 17
source: dbSNP
start: 73398210
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398211
feature_type: variation
id: rs774848751
seq_region_name: 17
source: dbSNP
start: 73398211
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398212
feature_type: variation
id: rs2062988513
seq_region_name: 17
source: dbSNP
start: 73398212
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398214
feature_type: variation
id: rs2145516177
seq_region_name: 17
source: dbSNP
start: 73398214
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398215
feature_type: variation
id: rs1191904823
seq_region_name: 17
source: dbSNP
start: 73398215
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398216
feature_type: variation
id: rs763620712
seq_region_name: 17
source: dbSNP
start: 73398216
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398218
feature_type: variation
id: rs1357368585
seq_region_name: 17
source: dbSNP
start: 73398218
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398219
feature_type: variation
id: rs576199502
seq_region_name: 17
source: dbSNP
start: 73398219
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398220
feature_type: variation
id: rs1321012820
seq_region_name: 17
source: dbSNP
start: 73398220
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398221
feature_type: variation
id: rs764952522
seq_region_name: 17
source: dbSNP
start: 73398221
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398224
feature_type: variation
id: rs2062988680
seq_region_name: 17
source: dbSNP
start: 73398224
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398228
feature_type: variation
id: rs1432414621
seq_region_name: 17
source: dbSNP
start: 73398228
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398229
feature_type: variation
id: rs750221097
seq_region_name: 17
source: dbSNP
start: 73398229
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398230
feature_type: variation
id: rs1371008947
seq_region_name: 17
source: dbSNP
start: 73398230
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398232
feature_type: variation
id: rs1220466210
seq_region_name: 17
source: dbSNP
start: 73398232
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398233
feature_type: variation
id: rs368569109
seq_region_name: 17
source: dbSNP
start: 73398233
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398235
feature_type: variation
id: rs1303993694
seq_region_name: 17
source: dbSNP
start: 73398235
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398240
feature_type: variation
id: rs936404157
seq_region_name: 17
source: dbSNP
start: 73398240
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398249
feature_type: variation
id: rs892763305
seq_region_name: 17
source: dbSNP
start: 73398249
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398252
feature_type: variation
id: rs1007243010
seq_region_name: 17
source: dbSNP
start: 73398252
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398255
feature_type: variation
id: rs2062988922
seq_region_name: 17
source: dbSNP
start: 73398255
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398260
feature_type: variation
id: rs1175947516
seq_region_name: 17
source: dbSNP
start: 73398260
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398267
feature_type: variation
id: rs2145516338
seq_region_name: 17
source: dbSNP
start: 73398263
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398264
feature_type: variation
id: rs2062988978
seq_region_name: 17
source: dbSNP
start: 73398264
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398267
feature_type: variation
id: rs1017709866
seq_region_name: 17
source: dbSNP
start: 73398267
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398268
feature_type: variation
id: rs965975602
seq_region_name: 17
source: dbSNP
start: 73398268
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398269
feature_type: variation
id: rs1390129729
seq_region_name: 17
source: dbSNP
start: 73398269
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398271
feature_type: variation
id: rs758324114
seq_region_name: 17
source: dbSNP
start: 73398271
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398272
feature_type: variation
id: rs879194195
seq_region_name: 17
source: dbSNP
start: 73398272
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398273
feature_type: variation
id: rs73999034
seq_region_name: 17
source: dbSNP
start: 73398273
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398277
feature_type: variation
id: rs1233211760
seq_region_name: 17
source: dbSNP
start: 73398273
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398277
feature_type: variation
id: rs2062989191
seq_region_name: 17
source: dbSNP
start: 73398277
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398278
feature_type: variation
id: rs1466573214
seq_region_name: 17
source: dbSNP
start: 73398278
strand: 1
-
alleles:
- AG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398279
feature_type: variation
id: rs2145516420
seq_region_name: 17
source: dbSNP
start: 73398278
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398279
feature_type: variation
id: rs2145516431
seq_region_name: 17
source: dbSNP
start: 73398279
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398284
feature_type: variation
id: rs1207050665
seq_region_name: 17
source: dbSNP
start: 73398284
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398288
feature_type: variation
id: rs374854161
seq_region_name: 17
source: dbSNP
start: 73398288
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398290
feature_type: variation
id: rs2062989298
seq_region_name: 17
source: dbSNP
start: 73398290
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398296
feature_type: variation
id: rs1488813237
seq_region_name: 17
source: dbSNP
start: 73398296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398301
feature_type: variation
id: rs749469513
seq_region_name: 17
source: dbSNP
start: 73398301
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398303
feature_type: variation
id: rs1026101103
seq_region_name: 17
source: dbSNP
start: 73398303
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398304
feature_type: variation
id: rs2291847
seq_region_name: 17
source: dbSNP
start: 73398304
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398305
feature_type: variation
id: rs1432493377
seq_region_name: 17
source: dbSNP
start: 73398305
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398306
feature_type: variation
id: rs779417469
seq_region_name: 17
source: dbSNP
start: 73398306
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398311
feature_type: variation
id: rs746293278
seq_region_name: 17
source: dbSNP
start: 73398311
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398313
feature_type: variation
id: rs772683463
seq_region_name: 17
source: dbSNP
start: 73398313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73398314
feature_type: variation
id: rs776105621
seq_region_name: 17
source: dbSNP
start: 73398314
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73398314
feature_type: variation
id: rs1568382179
seq_region_name: 17
source: dbSNP
start: 73398314
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73398316
feature_type: variation
id: rs1455450924
seq_region_name: 17
source: dbSNP
start: 73398316
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398322
feature_type: variation
id: rs2062989551
seq_region_name: 17
source: dbSNP
start: 73398322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398326
feature_type: variation
id: rs2145516576
seq_region_name: 17
source: dbSNP
start: 73398326
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398328
feature_type: variation
id: rs761116722
seq_region_name: 17
source: dbSNP
start: 73398328
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398329
feature_type: variation
id: rs768160250
seq_region_name: 17
source: dbSNP
start: 73398329
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398330
feature_type: variation
id: rs1599524479
seq_region_name: 17
source: dbSNP
start: 73398330
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398334
feature_type: variation
id: rs776014376
seq_region_name: 17
source: dbSNP
start: 73398334
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398337
feature_type: variation
id: rs148125243
seq_region_name: 17
source: dbSNP
start: 73398337
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398338
feature_type: variation
id: rs1599524497
seq_region_name: 17
source: dbSNP
start: 73398338
strand: 1
-
alleles:
- TT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73398339
feature_type: variation
id: rs35278118
seq_region_name: 17
source: dbSNP
start: 73398338
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398340
feature_type: variation
id: rs532578042
seq_region_name: 17
source: dbSNP
start: 73398340
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398343
feature_type: variation
id: rs2062989827
seq_region_name: 17
source: dbSNP
start: 73398343
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398345
feature_type: variation
id: rs201212596
seq_region_name: 17
source: dbSNP
start: 73398345
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398346
feature_type: variation
id: rs1296937318
seq_region_name: 17
source: dbSNP
start: 73398346
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73398347
feature_type: variation
id: rs141892877
seq_region_name: 17
source: dbSNP
start: 73398347
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398348
feature_type: variation
id: rs766122909
seq_region_name: 17
source: dbSNP
start: 73398348
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398349
feature_type: variation
id: rs559628757
seq_region_name: 17
source: dbSNP
start: 73398349
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398350
feature_type: variation
id: rs1599524535
seq_region_name: 17
source: dbSNP
start: 73398350
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398351
feature_type: variation
id: rs754885976
seq_region_name: 17
source: dbSNP
start: 73398351
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398354
feature_type: variation
id: rs2062990067
seq_region_name: 17
source: dbSNP
start: 73398354
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398357
feature_type: variation
id: rs2062990101
seq_region_name: 17
source: dbSNP
start: 73398357
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398359
feature_type: variation
id: rs1391026197
seq_region_name: 17
source: dbSNP
start: 73398359
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398362
feature_type: variation
id: rs530002288
seq_region_name: 17
source: dbSNP
start: 73398362
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398363
feature_type: variation
id: rs200483752
seq_region_name: 17
source: dbSNP
start: 73398363
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398364
feature_type: variation
id: rs757541604
seq_region_name: 17
source: dbSNP
start: 73398364
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398369
feature_type: variation
id: rs569887290
seq_region_name: 17
source: dbSNP
start: 73398369
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398370
feature_type: variation
id: rs780304075
seq_region_name: 17
source: dbSNP
start: 73398370
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398372
feature_type: variation
id: rs747489066
seq_region_name: 17
source: dbSNP
start: 73398372
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398376
feature_type: variation
id: rs769043748
seq_region_name: 17
source: dbSNP
start: 73398376
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398377
feature_type: variation
id: rs776197831
seq_region_name: 17
source: dbSNP
start: 73398377
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398378
feature_type: variation
id: rs530679709
seq_region_name: 17
source: dbSNP
start: 73398378
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398380
feature_type: variation
id: rs2062990454
seq_region_name: 17
source: dbSNP
start: 73398380
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398381
feature_type: variation
id: rs949611019
seq_region_name: 17
source: dbSNP
start: 73398381
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398385
feature_type: variation
id: rs1568382252
seq_region_name: 17
source: dbSNP
start: 73398385
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398394
feature_type: variation
id: rs1414313696
seq_region_name: 17
source: dbSNP
start: 73398394
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398397
feature_type: variation
id: rs375351502
seq_region_name: 17
source: dbSNP
start: 73398397
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398399
feature_type: variation
id: rs2062990623
seq_region_name: 17
source: dbSNP
start: 73398399
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398405
feature_type: variation
id: rs1024895719
seq_region_name: 17
source: dbSNP
start: 73398405
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73398406
feature_type: variation
id: rs147287702
seq_region_name: 17
source: dbSNP
start: 73398406
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398410
feature_type: variation
id: rs772813641
seq_region_name: 17
source: dbSNP
start: 73398410
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398411
feature_type: variation
id: rs1309103996
seq_region_name: 17
source: dbSNP
start: 73398411
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398417
feature_type: variation
id: rs2062990772
seq_region_name: 17
source: dbSNP
start: 73398417
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398419
feature_type: variation
id: rs2062990815
seq_region_name: 17
source: dbSNP
start: 73398419
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398421
feature_type: variation
id: rs1352885519
seq_region_name: 17
source: dbSNP
start: 73398421
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398422
feature_type: variation
id: rs2062990902
seq_region_name: 17
source: dbSNP
start: 73398422
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398423
feature_type: variation
id: rs552313285
seq_region_name: 17
source: dbSNP
start: 73398423
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73398424
feature_type: variation
id: rs371020440
seq_region_name: 17
source: dbSNP
start: 73398424
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73398428
feature_type: variation
id: rs1380409299
seq_region_name: 17
source: dbSNP
start: 73398428
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73398432
feature_type: variation
id: rs374164025
seq_region_name: 17
source: dbSNP
start: 73398432
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398438
feature_type: variation
id: rs759212658
seq_region_name: 17
source: dbSNP
start: 73398438
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73398446
feature_type: variation
id: rs2145517142
seq_region_name: 17
source: dbSNP
start: 73398446
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398447
feature_type: variation
id: rs1338968935
seq_region_name: 17
source: dbSNP
start: 73398447
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398448
feature_type: variation
id: rs767414270
seq_region_name: 17
source: dbSNP
start: 73398448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398449
feature_type: variation
id: rs199509466
seq_region_name: 17
source: dbSNP
start: 73398449
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398452
feature_type: variation
id: rs757451306
seq_region_name: 17
source: dbSNP
start: 73398452
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398457
feature_type: variation
id: rs765439084
seq_region_name: 17
source: dbSNP
start: 73398457
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398459
feature_type: variation
id: rs2062991189
seq_region_name: 17
source: dbSNP
start: 73398459
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398462
feature_type: variation
id: rs1231874654
seq_region_name: 17
source: dbSNP
start: 73398462
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398463
feature_type: variation
id: rs773216727
seq_region_name: 17
source: dbSNP
start: 73398462
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398464
feature_type: variation
id: rs750624163
seq_region_name: 17
source: dbSNP
start: 73398464
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398465
feature_type: variation
id: rs377687422
seq_region_name: 17
source: dbSNP
start: 73398465
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398466
feature_type: variation
id: rs1346400246
seq_region_name: 17
source: dbSNP
start: 73398466
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398467
feature_type: variation
id: rs1054588925
seq_region_name: 17
source: dbSNP
start: 73398467
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73398624
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73398627
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73398628
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73398631
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73398636
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73398640
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73398646
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73398654
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73398655
strand: 1
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alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73398656
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73398657
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73398660
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73398691
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398693
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73398694
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398697
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398698
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73398707
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs113663434
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strand: 1
-
alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- TT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398757
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145518034
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062993735
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- CCCAGGC
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398801
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398814
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398820
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1018026051
seq_region_name: 17
source: dbSNP
start: 73398821
strand: 1
-
alleles:
- AGAG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398826
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398831
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1210023648
seq_region_name: 17
source: dbSNP
start: 73398834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398835
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398837
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73398840
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398842
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398848
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs752017278
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs757625333
seq_region_name: 17
source: dbSNP
start: 73398854
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398855
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568382465
seq_region_name: 17
source: dbSNP
start: 73398856
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398861
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs970692070
seq_region_name: 17
source: dbSNP
start: 73398864
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062994489
seq_region_name: 17
source: dbSNP
start: 73398865
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1183133596
seq_region_name: 17
source: dbSNP
start: 73398869
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs954982801
seq_region_name: 17
source: dbSNP
start: 73398872
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398872
feature_type: variation
id: rs1599525094
seq_region_name: 17
source: dbSNP
start: 73398872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1471484328
seq_region_name: 17
source: dbSNP
start: 73398873
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73398879
strand: 1
-
alleles:
- CAGGGTACAG
- CAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062994647
seq_region_name: 17
source: dbSNP
start: 73398881
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs983708405
seq_region_name: 17
source: dbSNP
start: 73398883
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1407452199
seq_region_name: 17
source: dbSNP
start: 73398888
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062994727
seq_region_name: 17
source: dbSNP
start: 73398891
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398893
feature_type: variation
id: rs2062994755
seq_region_name: 17
source: dbSNP
start: 73398893
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398895
feature_type: variation
id: rs1417886770
seq_region_name: 17
source: dbSNP
start: 73398895
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs978067745
seq_region_name: 17
source: dbSNP
start: 73398897
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs189517591
seq_region_name: 17
source: dbSNP
start: 73398898
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398899
feature_type: variation
id: rs942211761
seq_region_name: 17
source: dbSNP
start: 73398899
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398900
feature_type: variation
id: rs1332160068
seq_region_name: 17
source: dbSNP
start: 73398900
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398902
feature_type: variation
id: rs2062994922
seq_region_name: 17
source: dbSNP
start: 73398902
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398903
feature_type: variation
id: rs1189963505
seq_region_name: 17
source: dbSNP
start: 73398903
strand: 1
-
alleles:
- TTTTT
- TTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398907
feature_type: variation
id: rs2062994974
seq_region_name: 17
source: dbSNP
start: 73398903
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398904
feature_type: variation
id: rs1466719778
seq_region_name: 17
source: dbSNP
start: 73398904
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398913
feature_type: variation
id: rs1568382497
seq_region_name: 17
source: dbSNP
start: 73398913
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398914
feature_type: variation
id: rs2062995019
seq_region_name: 17
source: dbSNP
start: 73398914
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398915
feature_type: variation
id: rs2062995052
seq_region_name: 17
source: dbSNP
start: 73398915
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398923
feature_type: variation
id: rs2062995093
seq_region_name: 17
source: dbSNP
start: 73398923
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398932
feature_type: variation
id: rs2062995121
seq_region_name: 17
source: dbSNP
start: 73398932
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398933
feature_type: variation
id: rs1245774170
seq_region_name: 17
source: dbSNP
start: 73398933
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73398936
feature_type: variation
id: rs1221768622
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- GTGTGTGTGTGT
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- GTGTGTGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- T
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- G
assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73399021
strand: 1
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alleles:
- GG
- G
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2062996542
seq_region_name: 17
source: dbSNP
start: 73399024
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs373001022
seq_region_name: 17
source: dbSNP
start: 73399041
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399045
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs886140968
seq_region_name: 17
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73399052
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73399053
strand: 1
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alleles:
- C
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399069
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399080
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399088
strand: 1
-
alleles:
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- AAATAAATA
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399089
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1018033679
seq_region_name: 17
source: dbSNP
start: 73399090
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs766808771
seq_region_name: 17
source: dbSNP
start: 73399097
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1012509658
seq_region_name: 17
source: dbSNP
start: 73399098
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062998003
seq_region_name: 17
source: dbSNP
start: 73399101
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1024836534
seq_region_name: 17
source: dbSNP
start: 73399102
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1466034126
seq_region_name: 17
source: dbSNP
start: 73399107
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062998075
seq_region_name: 17
source: dbSNP
start: 73399110
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs535040698
seq_region_name: 17
source: dbSNP
start: 73399115
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145519015
seq_region_name: 17
source: dbSNP
start: 73399116
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs769249180
seq_region_name: 17
source: dbSNP
start: 73399120
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs780178320
seq_region_name: 17
source: dbSNP
start: 73399121
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399123
feature_type: variation
id: rs1031005866
seq_region_name: 17
source: dbSNP
start: 73399123
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs554883042
seq_region_name: 17
source: dbSNP
start: 73399128
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2062998329
seq_region_name: 17
source: dbSNP
start: 73399130
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399131
feature_type: variation
id: rs879559749
seq_region_name: 17
source: dbSNP
start: 73399131
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399133
feature_type: variation
id: rs375971868
seq_region_name: 17
source: dbSNP
start: 73399133
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399134
feature_type: variation
id: rs749375572
seq_region_name: 17
source: dbSNP
start: 73399134
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399139
feature_type: variation
id: rs767456719
seq_region_name: 17
source: dbSNP
start: 73399139
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399145
feature_type: variation
id: rs775526362
seq_region_name: 17
source: dbSNP
start: 73399145
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399146
feature_type: variation
id: rs1599525362
seq_region_name: 17
source: dbSNP
start: 73399146
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399147
feature_type: variation
id: rs1204348021
seq_region_name: 17
source: dbSNP
start: 73399147
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399149
feature_type: variation
id: rs765349782
seq_region_name: 17
source: dbSNP
start: 73399149
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399150
feature_type: variation
id: rs1279245213
seq_region_name: 17
source: dbSNP
start: 73399149
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399150
feature_type: variation
id: rs750532283
seq_region_name: 17
source: dbSNP
start: 73399150
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399151
feature_type: variation
id: rs1236491807
seq_region_name: 17
source: dbSNP
start: 73399151
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399153
feature_type: variation
id: rs1449664490
seq_region_name: 17
source: dbSNP
start: 73399153
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399157
feature_type: variation
id: rs1474081079
seq_region_name: 17
source: dbSNP
start: 73399157
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73399161
feature_type: variation
id: rs2062998849
seq_region_name: 17
source: dbSNP
start: 73399161
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73399162
feature_type: variation
id: rs1190163368
seq_region_name: 17
source: dbSNP
start: 73399162
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73399166
feature_type: variation
id: rs758637505
seq_region_name: 17
source: dbSNP
start: 73399166
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399171
feature_type: variation
id: rs2062998945
seq_region_name: 17
source: dbSNP
start: 73399171
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399172
feature_type: variation
id: rs1418468537
seq_region_name: 17
source: dbSNP
start: 73399172
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399173
feature_type: variation
id: rs1448420287
seq_region_name: 17
source: dbSNP
start: 73399173
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73399187
feature_type: variation
id: rs766565174
seq_region_name: 17
source: dbSNP
start: 73399187
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399188
feature_type: variation
id: rs751928180
seq_region_name: 17
source: dbSNP
start: 73399188
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs2062999092
seq_region_name: 17
source: dbSNP
start: 73399196
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399199
feature_type: variation
id: rs2062999119
seq_region_name: 17
source: dbSNP
start: 73399199
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399200
feature_type: variation
id: rs1599525402
seq_region_name: 17
source: dbSNP
start: 73399200
strand: 1
-
alleles:
- TTTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73399203
feature_type: variation
id: rs866137593
seq_region_name: 17
source: dbSNP
start: 73399200
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399203
feature_type: variation
id: rs755261238
seq_region_name: 17
source: dbSNP
start: 73399203
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399207
feature_type: variation
id: rs781561860
seq_region_name: 17
source: dbSNP
start: 73399207
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73399209
feature_type: variation
id: rs748601515
seq_region_name: 17
source: dbSNP
start: 73399209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399210
feature_type: variation
id: rs201216905
seq_region_name: 17
source: dbSNP
start: 73399210
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399219
feature_type: variation
id: rs777262092
seq_region_name: 17
source: dbSNP
start: 73399219
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399220
feature_type: variation
id: rs71380175
seq_region_name: 17
source: dbSNP
start: 73399220
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399231
feature_type: variation
id: rs2062999540
seq_region_name: 17
source: dbSNP
start: 73399231
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399233
feature_type: variation
id: rs748855253
seq_region_name: 17
source: dbSNP
start: 73399233
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399241
feature_type: variation
id: rs200492062
seq_region_name: 17
source: dbSNP
start: 73399241
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399242
feature_type: variation
id: rs773917581
seq_region_name: 17
source: dbSNP
start: 73399242
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399243
feature_type: variation
id: rs577335730
seq_region_name: 17
source: dbSNP
start: 73399243
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399246
feature_type: variation
id: rs775438348
seq_region_name: 17
source: dbSNP
start: 73399246
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399248
feature_type: variation
id: rs200065270
seq_region_name: 17
source: dbSNP
start: 73399248
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399249
feature_type: variation
id: rs370582581
seq_region_name: 17
source: dbSNP
start: 73399249
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399252
feature_type: variation
id: rs1157766753
seq_region_name: 17
source: dbSNP
start: 73399252
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399253
feature_type: variation
id: rs2062999990
seq_region_name: 17
source: dbSNP
start: 73399253
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399255
feature_type: variation
id: rs2063000032
seq_region_name: 17
source: dbSNP
start: 73399255
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399260
feature_type: variation
id: rs773410204
seq_region_name: 17
source: dbSNP
start: 73399260
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399263
feature_type: variation
id: rs948145544
seq_region_name: 17
source: dbSNP
start: 73399263
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399271
feature_type: variation
id: rs377608354
seq_region_name: 17
source: dbSNP
start: 73399271
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399273
feature_type: variation
id: rs2063000235
seq_region_name: 17
source: dbSNP
start: 73399273
strand: 1
-
alleles:
- GGGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73399278
feature_type: variation
id: rs770900315
seq_region_name: 17
source: dbSNP
start: 73399273
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399276
feature_type: variation
id: rs933064005
seq_region_name: 17
source: dbSNP
start: 73399276
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399277
feature_type: variation
id: rs369561538
seq_region_name: 17
source: dbSNP
start: 73399277
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399278
feature_type: variation
id: rs983205823
seq_region_name: 17
source: dbSNP
start: 73399278
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73399279
feature_type: variation
id: rs139261927
seq_region_name: 17
source: dbSNP
start: 73399279
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73399287
feature_type: variation
id: rs941700917
seq_region_name: 17
source: dbSNP
start: 73399287
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73399291
feature_type: variation
id: rs1267656318
seq_region_name: 17
source: dbSNP
start: 73399291
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73399292
feature_type: variation
id: rs1429026304
seq_region_name: 17
source: dbSNP
start: 73399292
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73399299
feature_type: variation
id: rs139603654
seq_region_name: 17
source: dbSNP
start: 73399299
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73399304
feature_type: variation
id: rs767807054
seq_region_name: 17
source: dbSNP
start: 73399304
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73399305
feature_type: variation
id: rs1244528214
seq_region_name: 17
source: dbSNP
start: 73399305
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73399306
feature_type: variation
id: rs2145519814
seq_region_name: 17
source: dbSNP
start: 73399306
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399307
feature_type: variation
id: rs948024380
seq_region_name: 17
source: dbSNP
start: 73399307
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399309
feature_type: variation
id: rs1386751697
seq_region_name: 17
source: dbSNP
start: 73399309
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399309
feature_type: variation
id: rs2063000715
seq_region_name: 17
source: dbSNP
start: 73399309
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399310
feature_type: variation
id: rs2063000751
seq_region_name: 17
source: dbSNP
start: 73399310
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399311
feature_type: variation
id: rs2063000782
seq_region_name: 17
source: dbSNP
start: 73399311
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399312
feature_type: variation
id: rs1381675815
seq_region_name: 17
source: dbSNP
start: 73399312
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399313
feature_type: variation
id: rs1278311595
seq_region_name: 17
source: dbSNP
start: 73399313
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399315
feature_type: variation
id: rs1341390458
seq_region_name: 17
source: dbSNP
start: 73399315
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399316
feature_type: variation
id: rs756599650
seq_region_name: 17
source: dbSNP
start: 73399316
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399317
feature_type: variation
id: rs778303183
seq_region_name: 17
source: dbSNP
start: 73399317
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399322
feature_type: variation
id: rs2063001028
seq_region_name: 17
source: dbSNP
start: 73399322
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399323
feature_type: variation
id: rs777700024
seq_region_name: 17
source: dbSNP
start: 73399323
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399324
feature_type: variation
id: rs1282638497
seq_region_name: 17
source: dbSNP
start: 73399324
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399326
feature_type: variation
id: rs2145519968
seq_region_name: 17
source: dbSNP
start: 73399326
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399329
feature_type: variation
id: rs2063001155
seq_region_name: 17
source: dbSNP
start: 73399329
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399332
feature_type: variation
id: rs756680269
seq_region_name: 17
source: dbSNP
start: 73399332
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399333
feature_type: variation
id: rs2063001239
seq_region_name: 17
source: dbSNP
start: 73399333
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399334
feature_type: variation
id: rs1381090974
seq_region_name: 17
source: dbSNP
start: 73399334
strand: 1
-
alleles:
- CCCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399340
feature_type: variation
id: rs774074926
seq_region_name: 17
source: dbSNP
start: 73399335
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399336
feature_type: variation
id: rs574897966
seq_region_name: 17
source: dbSNP
start: 73399336
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399337
feature_type: variation
id: rs564797447
seq_region_name: 17
source: dbSNP
start: 73399337
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399338
feature_type: variation
id: rs2063001886
seq_region_name: 17
source: dbSNP
start: 73399338
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399339
feature_type: variation
id: rs2145520080
seq_region_name: 17
source: dbSNP
start: 73399339
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399340
feature_type: variation
id: rs2063001917
seq_region_name: 17
source: dbSNP
start: 73399340
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399341
feature_type: variation
id: rs1435132525
seq_region_name: 17
source: dbSNP
start: 73399341
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399342
feature_type: variation
id: rs2063002003
seq_region_name: 17
source: dbSNP
start: 73399342
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399344
feature_type: variation
id: rs2063002045
seq_region_name: 17
source: dbSNP
start: 73399344
strand: 1
-
alleles:
- GAACGGGACTGTTGGGCATGGAGGG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399370
feature_type: variation
id: rs2063002084
seq_region_name: 17
source: dbSNP
start: 73399346
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399349
feature_type: variation
id: rs1290930984
seq_region_name: 17
source: dbSNP
start: 73399349
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399350
feature_type: variation
id: rs112614181
seq_region_name: 17
source: dbSNP
start: 73399350
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399351
feature_type: variation
id: rs1457228910
seq_region_name: 17
source: dbSNP
start: 73399351
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399358
feature_type: variation
id: rs1196396820
seq_region_name: 17
source: dbSNP
start: 73399358
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399362
feature_type: variation
id: rs2063002250
seq_region_name: 17
source: dbSNP
start: 73399362
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399365
feature_type: variation
id: rs1368896383
seq_region_name: 17
source: dbSNP
start: 73399365
strand: 1
-
alleles:
- GGGGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399372
feature_type: variation
id: rs2063002322
seq_region_name: 17
source: dbSNP
start: 73399368
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399369
feature_type: variation
id: rs746984385
seq_region_name: 17
source: dbSNP
start: 73399369
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399370
feature_type: variation
id: rs1166644169
seq_region_name: 17
source: dbSNP
start: 73399370
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399374
feature_type: variation
id: rs2063002431
seq_region_name: 17
source: dbSNP
start: 73399374
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399377
feature_type: variation
id: rs2063002479
seq_region_name: 17
source: dbSNP
start: 73399377
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399378
feature_type: variation
id: rs866351190
seq_region_name: 17
source: dbSNP
start: 73399378
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399379
feature_type: variation
id: rs2063002556
seq_region_name: 17
source: dbSNP
start: 73399379
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399381
feature_type: variation
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73399514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399518
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399519
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399522
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399526
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399528
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399530
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399534
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399534
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1300509105
seq_region_name: 17
source: dbSNP
start: 73399535
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399536
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399538
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73399538
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73399541
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399543
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399544
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399545
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399548
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399551
strand: 1
-
alleles:
- AG
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399552
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399553
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399555
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063005033
seq_region_name: 17
source: dbSNP
start: 73399557
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1369786611
seq_region_name: 17
source: dbSNP
start: 73399558
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399559
feature_type: variation
id: rs969540770
seq_region_name: 17
source: dbSNP
start: 73399559
strand: 1
-
alleles:
- GGG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063005102
seq_region_name: 17
source: dbSNP
start: 73399559
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399560
feature_type: variation
id: rs951552652
seq_region_name: 17
source: dbSNP
start: 73399560
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399562
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399562
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399564
feature_type: variation
id: rs1284857014
seq_region_name: 17
source: dbSNP
start: 73399564
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399566
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399567
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399568
feature_type: variation
id: rs2145520908
seq_region_name: 17
source: dbSNP
start: 73399568
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399570
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73399570
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399572
feature_type: variation
id: rs2063005408
seq_region_name: 17
source: dbSNP
start: 73399572
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399578
feature_type: variation
id: rs2063005435
seq_region_name: 17
source: dbSNP
start: 73399578
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399580
feature_type: variation
id: rs1478375726
seq_region_name: 17
source: dbSNP
start: 73399580
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73399582
feature_type: variation
id: rs2063005497
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399812
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73399816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399820
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73399821
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73399823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1474088032
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alleles:
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400084
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400088
strand: 1
-
alleles:
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-
alleles:
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-
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-
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73400238
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400240
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73400241
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73400245
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73400249
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73400255
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73400260
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73400262
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73400265
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73400267
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73400270
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73400271
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73400276
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400277
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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start: 73400283
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400285
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400288
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400289
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400290
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400296
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400299
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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id: rs898630585
seq_region_name: 17
source: dbSNP
start: 73400304
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599526469
seq_region_name: 17
source: dbSNP
start: 73400307
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400308
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400309
feature_type: variation
id: rs1023578896
seq_region_name: 17
source: dbSNP
start: 73400309
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73400312
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400312
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400313
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400316
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id: rs904930040
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063012675
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73400443
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063012749
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73400453
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400455
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs986778091
seq_region_name: 17
source: dbSNP
start: 73400463
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1457182179
seq_region_name: 17
source: dbSNP
start: 73400467
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063012980
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063013006
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400475
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs934072581
seq_region_name: 17
source: dbSNP
start: 73400476
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063013068
seq_region_name: 17
source: dbSNP
start: 73400478
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063013091
seq_region_name: 17
source: dbSNP
start: 73400480
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs986846724
seq_region_name: 17
source: dbSNP
start: 73400481
strand: 1
-
alleles:
- GC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400485
feature_type: variation
id: rs1366117020
seq_region_name: 17
source: dbSNP
start: 73400484
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1165326461
seq_region_name: 17
source: dbSNP
start: 73400491
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs141071582
seq_region_name: 17
source: dbSNP
start: 73400496
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063013217
seq_region_name: 17
source: dbSNP
start: 73400497
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400500
feature_type: variation
id: rs961289348
seq_region_name: 17
source: dbSNP
start: 73400500
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1193951773
seq_region_name: 17
source: dbSNP
start: 73400502
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400503
feature_type: variation
id: rs1430568999
seq_region_name: 17
source: dbSNP
start: 73400503
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1295019184
seq_region_name: 17
source: dbSNP
start: 73400505
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400508
feature_type: variation
id: rs2063013338
seq_region_name: 17
source: dbSNP
start: 73400508
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400510
feature_type: variation
id: rs974330503
seq_region_name: 17
source: dbSNP
start: 73400510
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400511
feature_type: variation
id: rs1568383198
seq_region_name: 17
source: dbSNP
start: 73400511
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400511
feature_type: variation
id: rs1599526649
seq_region_name: 17
source: dbSNP
start: 73400511
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400513
feature_type: variation
id: rs539815343
seq_region_name: 17
source: dbSNP
start: 73400513
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400514
feature_type: variation
id: rs940048609
seq_region_name: 17
source: dbSNP
start: 73400514
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400516
feature_type: variation
id: rs867626775
seq_region_name: 17
source: dbSNP
start: 73400516
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400518
feature_type: variation
id: rs2145523556
seq_region_name: 17
source: dbSNP
start: 73400518
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400519
feature_type: variation
id: rs2063013537
seq_region_name: 17
source: dbSNP
start: 73400519
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400520
feature_type: variation
id: rs1568383212
seq_region_name: 17
source: dbSNP
start: 73400520
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400526
feature_type: variation
id: rs2063013596
seq_region_name: 17
source: dbSNP
start: 73400523
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400524
feature_type: variation
id: rs919739925
seq_region_name: 17
source: dbSNP
start: 73400524
strand: 1
-
alleles:
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- GGGAGCCACGGGAGCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400530
feature_type: variation
id: rs1490599185
seq_region_name: 17
source: dbSNP
start: 73400524
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400525
feature_type: variation
id: rs948480346
seq_region_name: 17
source: dbSNP
start: 73400525
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400531
feature_type: variation
id: rs114561882
seq_region_name: 17
source: dbSNP
start: 73400531
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400532
feature_type: variation
id: rs2063013696
seq_region_name: 17
source: dbSNP
start: 73400532
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400533
feature_type: variation
id: rs553043939
seq_region_name: 17
source: dbSNP
start: 73400532
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400536
feature_type: variation
id: rs2063013744
seq_region_name: 17
source: dbSNP
start: 73400536
strand: 1
-
alleles:
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seq_region_name: 17
source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
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strand: 1
-
alleles:
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400567
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400576
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs755136479
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs116929717
seq_region_name: 17
source: dbSNP
start: 73400592
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063014339
seq_region_name: 17
source: dbSNP
start: 73400601
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400610
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400611
strand: 1
-
alleles:
- T
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- C
- G
assembly_name: GRCh38
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feature_type: variation
id: rs1249255433
seq_region_name: 17
source: dbSNP
start: 73400614
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063014499
seq_region_name: 17
source: dbSNP
start: 73400618
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400625
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400626
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400630
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599526762
seq_region_name: 17
source: dbSNP
start: 73400635
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs997204849
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1028071437
seq_region_name: 17
source: dbSNP
start: 73400638
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599526774
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063014753
seq_region_name: 17
source: dbSNP
start: 73400647
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400650
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599526777
seq_region_name: 17
source: dbSNP
start: 73400653
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145524027
seq_region_name: 17
source: dbSNP
start: 73400654
strand: 1
-
alleles:
- TTTTT
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400655
strand: 1
-
alleles:
- TTATT
- TT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400658
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400660
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1253724760
seq_region_name: 17
source: dbSNP
start: 73400661
strand: 1
-
alleles:
- TTTTTTTTTTT
- TTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400661
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1222595293
seq_region_name: 17
source: dbSNP
start: 73400663
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400664
strand: 1
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alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063015157
seq_region_name: 17
source: dbSNP
start: 73400665
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs559659028
seq_region_name: 17
source: dbSNP
start: 73400665
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs758528889
seq_region_name: 17
source: dbSNP
start: 73400666
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400667
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400669
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400670
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400671
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1424572747
seq_region_name: 17
source: dbSNP
start: 73400672
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1470454984
seq_region_name: 17
source: dbSNP
start: 73400672
strand: 1
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alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs528768856
seq_region_name: 17
source: dbSNP
start: 73400673
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs547283278
seq_region_name: 17
source: dbSNP
start: 73400676
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1472428342
seq_region_name: 17
source: dbSNP
start: 73400677
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400678
feature_type: variation
id: rs568671089
seq_region_name: 17
source: dbSNP
start: 73400678
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400679
feature_type: variation
id: rs2063015813
seq_region_name: 17
source: dbSNP
start: 73400679
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400681
feature_type: variation
id: rs1441188168
seq_region_name: 17
source: dbSNP
start: 73400681
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400682
feature_type: variation
id: rs1253511262
seq_region_name: 17
source: dbSNP
start: 73400682
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400684
feature_type: variation
id: rs2063015949
seq_region_name: 17
source: dbSNP
start: 73400684
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400692
feature_type: variation
id: rs2063015988
seq_region_name: 17
source: dbSNP
start: 73400692
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400698
feature_type: variation
id: rs2063016011
seq_region_name: 17
source: dbSNP
start: 73400698
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400705
feature_type: variation
id: rs986816153
seq_region_name: 17
source: dbSNP
start: 73400705
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400708
feature_type: variation
id: rs562185204
seq_region_name: 17
source: dbSNP
start: 73400708
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400711
feature_type: variation
id: rs2063016113
seq_region_name: 17
source: dbSNP
start: 73400711
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400714
feature_type: variation
id: rs961783085
seq_region_name: 17
source: dbSNP
start: 73400714
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400715
feature_type: variation
id: rs1321130932
seq_region_name: 17
source: dbSNP
start: 73400715
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400716
feature_type: variation
id: rs2063016208
seq_region_name: 17
source: dbSNP
start: 73400716
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400717
feature_type: variation
id: rs755893437
seq_region_name: 17
source: dbSNP
start: 73400717
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400722
feature_type: variation
id: rs974087964
seq_region_name: 17
source: dbSNP
start: 73400722
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400723
feature_type: variation
id: rs1349763258
seq_region_name: 17
source: dbSNP
start: 73400723
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400725
feature_type: variation
id: rs2063016282
seq_region_name: 17
source: dbSNP
start: 73400725
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400727
feature_type: variation
id: rs919954886
seq_region_name: 17
source: dbSNP
start: 73400727
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400728
feature_type: variation
id: rs2063016339
seq_region_name: 17
source: dbSNP
start: 73400728
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400733
feature_type: variation
id: rs1428571995
seq_region_name: 17
source: dbSNP
start: 73400733
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400737
feature_type: variation
id: rs1338606166
seq_region_name: 17
source: dbSNP
start: 73400737
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400739
feature_type: variation
id: rs2063016408
seq_region_name: 17
source: dbSNP
start: 73400739
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400740
feature_type: variation
id: rs1287734250
seq_region_name: 17
source: dbSNP
start: 73400740
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400741
feature_type: variation
id: rs948996926
seq_region_name: 17
source: dbSNP
start: 73400741
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400749
feature_type: variation
id: rs2063016546
seq_region_name: 17
source: dbSNP
start: 73400749
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400750
feature_type: variation
id: rs1599526880
seq_region_name: 17
source: dbSNP
start: 73400750
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73400941
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73400946
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400947
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73400948
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400952
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400956
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400971
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400972
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400978
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400979
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73400979
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1449443810
seq_region_name: 17
source: dbSNP
start: 73400981
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400983
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400986
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73400989
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs745453127
seq_region_name: 17
source: dbSNP
start: 73400990
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400991
feature_type: variation
id: rs1049906905
seq_region_name: 17
source: dbSNP
start: 73400991
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400993
feature_type: variation
id: rs1410262977
seq_region_name: 17
source: dbSNP
start: 73400993
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400994
feature_type: variation
id: rs771855126
seq_region_name: 17
source: dbSNP
start: 73400994
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400995
feature_type: variation
id: rs779988173
seq_region_name: 17
source: dbSNP
start: 73400995
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400996
feature_type: variation
id: rs1392962342
seq_region_name: 17
source: dbSNP
start: 73400996
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400997
feature_type: variation
id: rs377531625
seq_region_name: 17
source: dbSNP
start: 73400997
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73400999
feature_type: variation
id: rs938940154
seq_region_name: 17
source: dbSNP
start: 73400999
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401000
feature_type: variation
id: rs1351066727
seq_region_name: 17
source: dbSNP
start: 73401000
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401004
feature_type: variation
id: rs1411626751
seq_region_name: 17
source: dbSNP
start: 73401004
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401005
feature_type: variation
id: rs2145525246
seq_region_name: 17
source: dbSNP
start: 73401005
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401006
feature_type: variation
id: rs1323063932
seq_region_name: 17
source: dbSNP
start: 73401006
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401010
feature_type: variation
id: rs1286204408
seq_region_name: 17
source: dbSNP
start: 73401010
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401011
feature_type: variation
id: rs1335011830
seq_region_name: 17
source: dbSNP
start: 73401011
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401012
feature_type: variation
id: rs1245065464
seq_region_name: 17
source: dbSNP
start: 73401012
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73401014
feature_type: variation
id: rs1266851325
seq_region_name: 17
source: dbSNP
start: 73401014
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73401015
feature_type: variation
id: rs1353579776
seq_region_name: 17
source: dbSNP
start: 73401015
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73401016
feature_type: variation
id: rs1221117580
seq_region_name: 17
source: dbSNP
start: 73401016
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401024
feature_type: variation
id: rs768690461
seq_region_name: 17
source: dbSNP
start: 73401024
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401026
feature_type: variation
id: rs2063019975
seq_region_name: 17
source: dbSNP
start: 73401026
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401028
feature_type: variation
id: rs2063019996
seq_region_name: 17
source: dbSNP
start: 73401028
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401029
feature_type: variation
id: rs1185033156
seq_region_name: 17
source: dbSNP
start: 73401029
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73401032
feature_type: variation
id: rs1483648756
seq_region_name: 17
source: dbSNP
start: 73401029
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401032
feature_type: variation
id: rs867011026
seq_region_name: 17
source: dbSNP
start: 73401032
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401033
feature_type: variation
id: rs1248841816
seq_region_name: 17
source: dbSNP
start: 73401033
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401036
feature_type: variation
id: rs1418926836
seq_region_name: 17
source: dbSNP
start: 73401036
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401037
feature_type: variation
id: rs1407108648
seq_region_name: 17
source: dbSNP
start: 73401037
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401039
feature_type: variation
id: rs1188427308
seq_region_name: 17
source: dbSNP
start: 73401039
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401041
feature_type: variation
id: rs1053269584
seq_region_name: 17
source: dbSNP
start: 73401041
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401042
feature_type: variation
id: rs1370430163
seq_region_name: 17
source: dbSNP
start: 73401042
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401045
feature_type: variation
id: rs2063020305
seq_region_name: 17
source: dbSNP
start: 73401045
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401046
feature_type: variation
id: rs2063020336
seq_region_name: 17
source: dbSNP
start: 73401046
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401050
feature_type: variation
id: rs867814181
seq_region_name: 17
source: dbSNP
start: 73401050
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73401051
feature_type: variation
id: rs201256089
seq_region_name: 17
source: dbSNP
start: 73401051
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401056
feature_type: variation
id: rs761835533
seq_region_name: 17
source: dbSNP
start: 73401056
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401059
feature_type: variation
id: rs1471180169
seq_region_name: 17
source: dbSNP
start: 73401059
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401060
feature_type: variation
id: rs1431537377
seq_region_name: 17
source: dbSNP
start: 73401060
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401061
feature_type: variation
id: rs2063020498
seq_region_name: 17
source: dbSNP
start: 73401061
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401062
feature_type: variation
id: rs370497188
seq_region_name: 17
source: dbSNP
start: 73401062
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401063
feature_type: variation
id: rs2063020607
seq_region_name: 17
source: dbSNP
start: 73401063
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401064
feature_type: variation
id: rs774496820
seq_region_name: 17
source: dbSNP
start: 73401064
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401066
feature_type: variation
id: rs1159376466
seq_region_name: 17
source: dbSNP
start: 73401066
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401067
feature_type: variation
id: rs1396408581
seq_region_name: 17
source: dbSNP
start: 73401067
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401076
feature_type: variation
id: rs1037116777
seq_region_name: 17
source: dbSNP
start: 73401076
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401078
feature_type: variation
id: rs1428102503
seq_region_name: 17
source: dbSNP
start: 73401078
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401080
feature_type: variation
id: rs945103878
seq_region_name: 17
source: dbSNP
start: 73401080
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401083
feature_type: variation
id: rs759676394
seq_region_name: 17
source: dbSNP
start: 73401083
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73401084
feature_type: variation
id: rs143289914
seq_region_name: 17
source: dbSNP
start: 73401084
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401085
feature_type: variation
id: rs1244836559
seq_region_name: 17
source: dbSNP
start: 73401085
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401086
feature_type: variation
id: rs1297665539
seq_region_name: 17
source: dbSNP
start: 73401086
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401087
feature_type: variation
id: rs753038326
seq_region_name: 17
source: dbSNP
start: 73401087
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401090
feature_type: variation
id: rs1207912357
seq_region_name: 17
source: dbSNP
start: 73401090
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401091
feature_type: variation
id: rs199750691
seq_region_name: 17
source: dbSNP
start: 73401091
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401092
feature_type: variation
id: rs201665128
seq_region_name: 17
source: dbSNP
start: 73401092
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401093
feature_type: variation
id: rs754248280
seq_region_name: 17
source: dbSNP
start: 73401093
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401095
feature_type: variation
id: rs866277042
seq_region_name: 17
source: dbSNP
start: 73401095
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401098
feature_type: variation
id: rs757794209
seq_region_name: 17
source: dbSNP
start: 73401098
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401104
feature_type: variation
id: rs1599527352
seq_region_name: 17
source: dbSNP
start: 73401104
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401106
feature_type: variation
id: rs2063021489
seq_region_name: 17
source: dbSNP
start: 73401106
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401108
feature_type: variation
id: rs778217970
seq_region_name: 17
source: dbSNP
start: 73401108
strand: 1
-
alleles:
- GAG
- GAGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73401110
feature_type: variation
id: rs1183285365
seq_region_name: 17
source: dbSNP
start: 73401108
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401110
feature_type: variation
id: rs1208052881
seq_region_name: 17
source: dbSNP
start: 73401110
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73401111
feature_type: variation
id: rs114429753
seq_region_name: 17
source: dbSNP
start: 73401111
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401112
feature_type: variation
id: rs139022524
seq_region_name: 17
source: dbSNP
start: 73401112
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401113
feature_type: variation
id: rs746767238
seq_region_name: 17
source: dbSNP
start: 73401113
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401114
feature_type: variation
id: rs754774087
seq_region_name: 17
source: dbSNP
start: 73401114
strand: 1
-
alleles:
- T
- TATCTCGGCTCGCTGCAACCTCTACCTCCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73401116
feature_type: variation
id: rs767200339
seq_region_name: 17
source: dbSNP
start: 73401116
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401117
feature_type: variation
id: rs781057087
seq_region_name: 17
source: dbSNP
start: 73401117
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401121
feature_type: variation
id: rs1399856678
seq_region_name: 17
source: dbSNP
start: 73401121
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401122
feature_type: variation
id: rs959894011
seq_region_name: 17
source: dbSNP
start: 73401122
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401123
feature_type: variation
id: rs145375289
seq_region_name: 17
source: dbSNP
start: 73401123
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401124
feature_type: variation
id: rs1320889649
seq_region_name: 17
source: dbSNP
start: 73401124
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401130
feature_type: variation
id: rs769841452
seq_region_name: 17
source: dbSNP
start: 73401130
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401131
feature_type: variation
id: rs143950228
seq_region_name: 17
source: dbSNP
start: 73401131
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401135
feature_type: variation
id: rs1293997313
seq_region_name: 17
source: dbSNP
start: 73401135
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401139
feature_type: variation
id: rs1307395483
seq_region_name: 17
source: dbSNP
start: 73401139
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401146
feature_type: variation
id: rs201204055
seq_region_name: 17
source: dbSNP
start: 73401146
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401147
feature_type: variation
id: rs79432016
seq_region_name: 17
source: dbSNP
start: 73401147
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401150
feature_type: variation
id: rs775651709
seq_region_name: 17
source: dbSNP
start: 73401150
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401152
feature_type: variation
id: rs1203199022
seq_region_name: 17
source: dbSNP
start: 73401152
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401153
feature_type: variation
id: rs760907273
seq_region_name: 17
source: dbSNP
start: 73401153
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401158
feature_type: variation
id: rs1466274258
seq_region_name: 17
source: dbSNP
start: 73401158
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401163
feature_type: variation
id: rs1184893687
seq_region_name: 17
source: dbSNP
start: 73401163
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401169
feature_type: variation
id: rs764382713
seq_region_name: 17
source: dbSNP
start: 73401169
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
- likely benign
consequence_type: missense_variant
end: 73401170
feature_type: variation
id: rs143280778
seq_region_name: 17
source: dbSNP
start: 73401170
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73401171
feature_type: variation
id: rs146716999
seq_region_name: 17
source: dbSNP
start: 73401171
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401174
feature_type: variation
id: rs1426935291
seq_region_name: 17
source: dbSNP
start: 73401174
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401175
feature_type: variation
id: rs140355408
seq_region_name: 17
source: dbSNP
start: 73401175
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401177
feature_type: variation
id: rs954322965
seq_region_name: 17
source: dbSNP
start: 73401177
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
- likely benign
consequence_type: missense_variant
end: 73401181
feature_type: variation
id: rs144141099
seq_region_name: 17
source: dbSNP
start: 73401181
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73401182
feature_type: variation
id: rs151020640
seq_region_name: 17
source: dbSNP
start: 73401182
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401185
feature_type: variation
id: rs1287759312
seq_region_name: 17
source: dbSNP
start: 73401185
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73401186
feature_type: variation
id: rs1243813859
seq_region_name: 17
source: dbSNP
start: 73401186
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73401187
feature_type: variation
id: rs137921116
seq_region_name: 17
source: dbSNP
start: 73401187
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401188
feature_type: variation
id: rs1599527542
seq_region_name: 17
source: dbSNP
start: 73401188
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401190
feature_type: variation
id: rs766016014
seq_region_name: 17
source: dbSNP
start: 73401190
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401198
feature_type: variation
id: rs551555608
seq_region_name: 17
source: dbSNP
start: 73401198
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401201
feature_type: variation
id: rs1321785203
seq_region_name: 17
source: dbSNP
start: 73401201
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401205
feature_type: variation
id: rs191033175
seq_region_name: 17
source: dbSNP
start: 73401205
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401206
feature_type: variation
id: rs754685995
seq_region_name: 17
source: dbSNP
start: 73401206
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401209
feature_type: variation
id: rs1599527572
seq_region_name: 17
source: dbSNP
start: 73401209
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401210
feature_type: variation
id: rs1331450361
seq_region_name: 17
source: dbSNP
start: 73401210
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73401212
feature_type: variation
id: rs1213972093
seq_region_name: 17
source: dbSNP
start: 73401212
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401218
feature_type: variation
id: rs1260202686
seq_region_name: 17
source: dbSNP
start: 73401218
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401219
feature_type: variation
id: rs780848004
seq_region_name: 17
source: dbSNP
start: 73401219
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401221
feature_type: variation
id: rs1192779914
seq_region_name: 17
source: dbSNP
start: 73401221
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401223
feature_type: variation
id: rs1266697835
seq_region_name: 17
source: dbSNP
start: 73401223
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401224
feature_type: variation
id: rs199991088
seq_region_name: 17
source: dbSNP
start: 73401224
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401226
feature_type: variation
id: rs555284148
seq_region_name: 17
source: dbSNP
start: 73401226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401227
feature_type: variation
id: rs11653524
seq_region_name: 17
source: dbSNP
start: 73401227
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401232
feature_type: variation
id: rs202096993
seq_region_name: 17
source: dbSNP
start: 73401232
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401236
feature_type: variation
id: rs7226251
seq_region_name: 17
source: dbSNP
start: 73401236
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401237
feature_type: variation
id: rs1349889271
seq_region_name: 17
source: dbSNP
start: 73401237
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401242
feature_type: variation
id: rs1288106021
seq_region_name: 17
source: dbSNP
start: 73401242
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401243
feature_type: variation
id: rs374297809
seq_region_name: 17
source: dbSNP
start: 73401243
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401244
feature_type: variation
id: rs1305443902
seq_region_name: 17
source: dbSNP
start: 73401244
strand: 1
-
alleles:
- TGTGAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401251
feature_type: variation
id: rs1368085953
seq_region_name: 17
source: dbSNP
start: 73401246
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401249
feature_type: variation
id: rs577732899
seq_region_name: 17
source: dbSNP
start: 73401249
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401251
feature_type: variation
id: rs1404927701
seq_region_name: 17
source: dbSNP
start: 73401251
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401257
feature_type: variation
id: rs1303646646
seq_region_name: 17
source: dbSNP
start: 73401257
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401260
feature_type: variation
id: rs1325535618
seq_region_name: 17
source: dbSNP
start: 73401260
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401264
feature_type: variation
id: rs1699343363
seq_region_name: 17
source: dbSNP
start: 73401264
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401267
feature_type: variation
id: rs2063023634
seq_region_name: 17
source: dbSNP
start: 73401267
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401269
feature_type: variation
id: rs2145526585
seq_region_name: 17
source: dbSNP
start: 73401267
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401268
feature_type: variation
id: rs1443933771
seq_region_name: 17
source: dbSNP
start: 73401268
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401270
feature_type: variation
id: rs2145526606
seq_region_name: 17
source: dbSNP
start: 73401270
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401273
feature_type: variation
id: rs1837054201
seq_region_name: 17
source: dbSNP
start: 73401273
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401274
feature_type: variation
id: rs1385979453
seq_region_name: 17
source: dbSNP
start: 73401274
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401276
feature_type: variation
id: rs979179850
seq_region_name: 17
source: dbSNP
start: 73401276
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401284
feature_type: variation
id: rs1568383705
seq_region_name: 17
source: dbSNP
start: 73401284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401289
feature_type: variation
id: rs2063023747
seq_region_name: 17
source: dbSNP
start: 73401289
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401290
feature_type: variation
id: rs1426981262
seq_region_name: 17
source: dbSNP
start: 73401290
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401297
feature_type: variation
id: rs1599527678
seq_region_name: 17
source: dbSNP
start: 73401297
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401298
feature_type: variation
id: rs538750806
seq_region_name: 17
source: dbSNP
start: 73401298
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401301
feature_type: variation
id: rs1010082033
seq_region_name: 17
source: dbSNP
start: 73401301
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401308
feature_type: variation
id: rs2145526686
seq_region_name: 17
source: dbSNP
start: 73401308
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401312
feature_type: variation
id: rs1370320400
seq_region_name: 17
source: dbSNP
start: 73401312
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401315
feature_type: variation
id: rs758404092
seq_region_name: 17
source: dbSNP
start: 73401315
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401316
feature_type: variation
id: rs1487020104
seq_region_name: 17
source: dbSNP
start: 73401316
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401317
feature_type: variation
id: rs2145526716
seq_region_name: 17
source: dbSNP
start: 73401317
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401318
feature_type: variation
id: rs1290026848
seq_region_name: 17
source: dbSNP
start: 73401318
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401320
feature_type: variation
id: rs2145526740
seq_region_name: 17
source: dbSNP
start: 73401320
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401332
feature_type: variation
id: rs2063023965
seq_region_name: 17
source: dbSNP
start: 73401332
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401338
feature_type: variation
id: rs2063023997
seq_region_name: 17
source: dbSNP
start: 73401338
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401341
feature_type: variation
id: rs1599527703
seq_region_name: 17
source: dbSNP
start: 73401341
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401342
feature_type: variation
id: rs1599527707
seq_region_name: 17
source: dbSNP
start: 73401342
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401344
feature_type: variation
id: rs369686989
seq_region_name: 17
source: dbSNP
start: 73401344
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401345
feature_type: variation
id: rs553543504
seq_region_name: 17
source: dbSNP
start: 73401345
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401346
feature_type: variation
id: rs1360767664
seq_region_name: 17
source: dbSNP
start: 73401346
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401347
feature_type: variation
id: rs1020511566
seq_region_name: 17
source: dbSNP
start: 73401347
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401348
feature_type: variation
id: rs2063024180
seq_region_name: 17
source: dbSNP
start: 73401348
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401349
feature_type: variation
id: rs2034817922
seq_region_name: 17
source: dbSNP
start: 73401349
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401350
feature_type: variation
id: rs1247485431
seq_region_name: 17
source: dbSNP
start: 73401350
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401353
feature_type: variation
id: rs2063024204
seq_region_name: 17
source: dbSNP
start: 73401353
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401354
feature_type: variation
id: rs968461818
seq_region_name: 17
source: dbSNP
start: 73401354
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401363
feature_type: variation
id: rs2063024256
seq_region_name: 17
source: dbSNP
start: 73401363
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401366
feature_type: variation
id: rs1294340536
seq_region_name: 17
source: dbSNP
start: 73401366
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401367
feature_type: variation
id: rs1272006691
seq_region_name: 17
source: dbSNP
start: 73401367
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401379
feature_type: variation
id: rs572108944
seq_region_name: 17
source: dbSNP
start: 73401379
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401380
feature_type: variation
id: rs999887736
seq_region_name: 17
source: dbSNP
start: 73401380
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401384
feature_type: variation
id: rs2063024402
seq_region_name: 17
source: dbSNP
start: 73401384
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401390
feature_type: variation
id: rs2063024435
seq_region_name: 17
source: dbSNP
start: 73401390
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401391
feature_type: variation
id: rs2145526863
seq_region_name: 17
source: dbSNP
start: 73401391
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401393
feature_type: variation
id: rs1028649038
seq_region_name: 17
source: dbSNP
start: 73401393
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401397
feature_type: variation
id: rs2063024486
seq_region_name: 17
source: dbSNP
start: 73401397
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401399
feature_type: variation
id: rs1599527757
seq_region_name: 17
source: dbSNP
start: 73401399
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401403
feature_type: variation
id: rs1423988727
seq_region_name: 17
source: dbSNP
start: 73401403
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401406
feature_type: variation
id: rs890832133
seq_region_name: 17
source: dbSNP
start: 73401406
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401407
feature_type: variation
id: rs2063024589
seq_region_name: 17
source: dbSNP
start: 73401407
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401408
feature_type: variation
id: rs2063024617
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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id: rs78286639
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1372733756
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs1211727819
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063024824
seq_region_name: 17
source: dbSNP
start: 73401422
strand: 1
-
alleles:
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- AGT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs149091394
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145526987
seq_region_name: 17
source: dbSNP
start: 73401424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145526995
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1430517786
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1267272247
seq_region_name: 17
source: dbSNP
start: 73401432
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063024936
seq_region_name: 17
source: dbSNP
start: 73401434
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599527803
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs62072143
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs896959063
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs995766253
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599527825
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs1026844822
seq_region_name: 17
source: dbSNP
start: 73401448
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs965986341
seq_region_name: 17
source: dbSNP
start: 73401450
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1250267440
seq_region_name: 17
source: dbSNP
start: 73401453
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs972945508
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599527843
seq_region_name: 17
source: dbSNP
start: 73401460
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063025265
seq_region_name: 17
source: dbSNP
start: 73401462
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599527846
seq_region_name: 17
source: dbSNP
start: 73401464
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1474856050
seq_region_name: 17
source: dbSNP
start: 73401468
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs905935131
seq_region_name: 17
source: dbSNP
start: 73401469
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1163527198
seq_region_name: 17
source: dbSNP
start: 73401472
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs111794820
seq_region_name: 17
source: dbSNP
start: 73401473
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs931416410
seq_region_name: 17
source: dbSNP
start: 73401476
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401477
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063025469
seq_region_name: 17
source: dbSNP
start: 73401482
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs574370706
seq_region_name: 17
source: dbSNP
start: 73401483
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599527871
seq_region_name: 17
source: dbSNP
start: 73401485
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs570626550
seq_region_name: 17
source: dbSNP
start: 73401487
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1304817247
seq_region_name: 17
source: dbSNP
start: 73401489
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063025617
seq_region_name: 17
source: dbSNP
start: 73401491
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063025644
seq_region_name: 17
source: dbSNP
start: 73401497
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs937330558
seq_region_name: 17
source: dbSNP
start: 73401499
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1395945595
seq_region_name: 17
source: dbSNP
start: 73401501
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599527896
seq_region_name: 17
source: dbSNP
start: 73401504
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1436484532
seq_region_name: 17
source: dbSNP
start: 73401506
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1320321585
seq_region_name: 17
source: dbSNP
start: 73401509
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1324800126
seq_region_name: 17
source: dbSNP
start: 73401512
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1168547063
seq_region_name: 17
source: dbSNP
start: 73401513
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401514
feature_type: variation
id: rs989046402
seq_region_name: 17
source: dbSNP
start: 73401514
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1226940272
seq_region_name: 17
source: dbSNP
start: 73401516
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1176169555
seq_region_name: 17
source: dbSNP
start: 73401517
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1480936349
seq_region_name: 17
source: dbSNP
start: 73401518
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401519
feature_type: variation
id: rs1431891123
seq_region_name: 17
source: dbSNP
start: 73401519
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401525
feature_type: variation
id: rs1057433806
seq_region_name: 17
source: dbSNP
start: 73401525
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401535
feature_type: variation
id: rs1437730353
seq_region_name: 17
source: dbSNP
start: 73401535
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401537
feature_type: variation
id: rs1249261236
seq_region_name: 17
source: dbSNP
start: 73401537
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401541
feature_type: variation
id: rs2063026008
seq_region_name: 17
source: dbSNP
start: 73401541
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145527310
seq_region_name: 17
source: dbSNP
start: 73401543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401544
feature_type: variation
id: rs1195817616
seq_region_name: 17
source: dbSNP
start: 73401544
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401547
feature_type: variation
id: rs2063026051
seq_region_name: 17
source: dbSNP
start: 73401547
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401549
feature_type: variation
id: rs2063026085
seq_region_name: 17
source: dbSNP
start: 73401549
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401553
feature_type: variation
id: rs181119316
seq_region_name: 17
source: dbSNP
start: 73401553
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401554
feature_type: variation
id: rs2063026136
seq_region_name: 17
source: dbSNP
start: 73401554
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401555
feature_type: variation
id: rs2063026160
seq_region_name: 17
source: dbSNP
start: 73401555
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401556
feature_type: variation
id: rs2063026190
seq_region_name: 17
source: dbSNP
start: 73401556
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401559
feature_type: variation
id: rs945933780
seq_region_name: 17
source: dbSNP
start: 73401559
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401560
feature_type: variation
id: rs2063026236
seq_region_name: 17
source: dbSNP
start: 73401560
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401570
feature_type: variation
id: rs1222684916
seq_region_name: 17
source: dbSNP
start: 73401570
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401572
feature_type: variation
id: rs1324072818
seq_region_name: 17
source: dbSNP
start: 73401572
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401573
feature_type: variation
id: rs1020972695
seq_region_name: 17
source: dbSNP
start: 73401573
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401574
feature_type: variation
id: rs2063026340
seq_region_name: 17
source: dbSNP
start: 73401575
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401577
feature_type: variation
id: rs2063026361
seq_region_name: 17
source: dbSNP
start: 73401577
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401579
feature_type: variation
id: rs2063026386
seq_region_name: 17
source: dbSNP
start: 73401579
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401582
feature_type: variation
id: rs1276392673
seq_region_name: 17
source: dbSNP
start: 73401582
strand: 1
-
alleles:
- CAGGGGATGGACCAGCTCTGACCTTTCCCAGCCCTGTCCTGCCCTCTGGTTCAG
- CAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401635
feature_type: variation
id: rs1568383794
seq_region_name: 17
source: dbSNP
start: 73401582
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401585
feature_type: variation
id: rs969019617
seq_region_name: 17
source: dbSNP
start: 73401585
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401587
feature_type: variation
id: rs2063026478
seq_region_name: 17
source: dbSNP
start: 73401587
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401589
feature_type: variation
id: rs1336663901
seq_region_name: 17
source: dbSNP
start: 73401589
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401591
feature_type: variation
id: rs2063026530
seq_region_name: 17
source: dbSNP
start: 73401591
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401593
feature_type: variation
id: rs2145527474
seq_region_name: 17
source: dbSNP
start: 73401593
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401599
feature_type: variation
id: rs2063026550
seq_region_name: 17
source: dbSNP
start: 73401599
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401602
feature_type: variation
id: rs1599527980
seq_region_name: 17
source: dbSNP
start: 73401602
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401603
feature_type: variation
id: rs2063026602
seq_region_name: 17
source: dbSNP
start: 73401603
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401605
feature_type: variation
id: rs1224945462
seq_region_name: 17
source: dbSNP
start: 73401605
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401606
feature_type: variation
id: rs1289347227
seq_region_name: 17
source: dbSNP
start: 73401606
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401610
feature_type: variation
id: rs74657905
seq_region_name: 17
source: dbSNP
start: 73401610
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401613
feature_type: variation
id: rs2063026704
seq_region_name: 17
source: dbSNP
start: 73401613
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401619
feature_type: variation
id: rs371905050
seq_region_name: 17
source: dbSNP
start: 73401619
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401620
feature_type: variation
id: rs1283829414
seq_region_name: 17
source: dbSNP
start: 73401620
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401622
feature_type: variation
id: rs747166280
seq_region_name: 17
source: dbSNP
start: 73401622
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401623
feature_type: variation
id: rs753569056
seq_region_name: 17
source: dbSNP
start: 73401623
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401627
feature_type: variation
id: rs768988267
seq_region_name: 17
source: dbSNP
start: 73401627
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401630
feature_type: variation
id: rs533316548
seq_region_name: 17
source: dbSNP
start: 73401630
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401633
feature_type: variation
id: rs1205856968
seq_region_name: 17
source: dbSNP
start: 73401633
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401639
feature_type: variation
id: rs1253700711
seq_region_name: 17
source: dbSNP
start: 73401639
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401640
feature_type: variation
id: rs2063026938
seq_region_name: 17
source: dbSNP
start: 73401640
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401643
feature_type: variation
id: rs2063026962
seq_region_name: 17
source: dbSNP
start: 73401643
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401645
feature_type: variation
id: rs775080595
seq_region_name: 17
source: dbSNP
start: 73401645
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401646
feature_type: variation
id: rs762282991
seq_region_name: 17
source: dbSNP
start: 73401646
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73401649
feature_type: variation
id: rs2063027058
seq_region_name: 17
source: dbSNP
start: 73401649
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73401650
feature_type: variation
id: rs1176212486
seq_region_name: 17
source: dbSNP
start: 73401650
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73401651
feature_type: variation
id: rs1404198268
seq_region_name: 17
source: dbSNP
start: 73401651
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73401653
feature_type: variation
id: rs1414098211
seq_region_name: 17
source: dbSNP
start: 73401653
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401656
feature_type: variation
id: rs765628138
seq_region_name: 17
source: dbSNP
start: 73401656
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401657
feature_type: variation
id: rs150389540
seq_region_name: 17
source: dbSNP
start: 73401657
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401658
feature_type: variation
id: rs1364469136
seq_region_name: 17
source: dbSNP
start: 73401658
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401661
feature_type: variation
id: rs1424565196
seq_region_name: 17
source: dbSNP
start: 73401661
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73401663
feature_type: variation
id: rs879056608
seq_region_name: 17
source: dbSNP
start: 73401663
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401664
feature_type: variation
id: rs1309234824
seq_region_name: 17
source: dbSNP
start: 73401664
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73401667
feature_type: variation
id: rs760195883
seq_region_name: 17
source: dbSNP
start: 73401667
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401667
feature_type: variation
id: rs763571312
seq_region_name: 17
source: dbSNP
start: 73401667
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401671
feature_type: variation
id: rs2063027406
seq_region_name: 17
source: dbSNP
start: 73401671
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401673
feature_type: variation
id: rs1279134323
seq_region_name: 17
source: dbSNP
start: 73401673
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401675
feature_type: variation
id: rs1380205242
seq_region_name: 17
source: dbSNP
start: 73401675
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401677
feature_type: variation
id: rs1248494677
seq_region_name: 17
source: dbSNP
start: 73401677
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401678
feature_type: variation
id: rs754858539
seq_region_name: 17
source: dbSNP
start: 73401678
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401679
feature_type: variation
id: rs751184968
seq_region_name: 17
source: dbSNP
start: 73401679
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401680
feature_type: variation
id: rs754667948
seq_region_name: 17
source: dbSNP
start: 73401680
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401682
feature_type: variation
id: rs868080945
seq_region_name: 17
source: dbSNP
start: 73401682
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73401686
feature_type: variation
id: rs138152327
seq_region_name: 17
source: dbSNP
start: 73401686
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401691
feature_type: variation
id: rs1435819151
seq_region_name: 17
source: dbSNP
start: 73401691
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401692
feature_type: variation
id: rs2063027704
seq_region_name: 17
source: dbSNP
start: 73401692
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401695
feature_type: variation
id: rs752403711
seq_region_name: 17
source: dbSNP
start: 73401695
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401697
feature_type: variation
id: rs755899464
seq_region_name: 17
source: dbSNP
start: 73401697
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401703
feature_type: variation
id: rs777452561
seq_region_name: 17
source: dbSNP
start: 73401703
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401704
feature_type: variation
id: rs753714901
seq_region_name: 17
source: dbSNP
start: 73401704
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401709
feature_type: variation
id: rs1384066807
seq_region_name: 17
source: dbSNP
start: 73401709
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401710
feature_type: variation
id: rs1449545143
seq_region_name: 17
source: dbSNP
start: 73401710
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401711
feature_type: variation
id: rs1169717078
seq_region_name: 17
source: dbSNP
start: 73401711
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401712
feature_type: variation
id: rs1422297111
seq_region_name: 17
source: dbSNP
start: 73401712
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401714
feature_type: variation
id: rs1408531767
seq_region_name: 17
source: dbSNP
start: 73401714
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401715
feature_type: variation
id: rs1328565070
seq_region_name: 17
source: dbSNP
start: 73401715
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401718
feature_type: variation
id: rs1008577296
seq_region_name: 17
source: dbSNP
start: 73401718
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401722
feature_type: variation
id: rs1454777849
seq_region_name: 17
source: dbSNP
start: 73401722
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401723
feature_type: variation
id: rs757189650
seq_region_name: 17
source: dbSNP
start: 73401723
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401724
feature_type: variation
id: rs1382053681
seq_region_name: 17
source: dbSNP
start: 73401724
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401725
feature_type: variation
id: rs780101980
seq_region_name: 17
source: dbSNP
start: 73401725
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401726
feature_type: variation
id: rs2063028209
seq_region_name: 17
source: dbSNP
start: 73401726
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401727
feature_type: variation
id: rs747149865
seq_region_name: 17
source: dbSNP
start: 73401727
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401730
feature_type: variation
id: rs1240713590
seq_region_name: 17
source: dbSNP
start: 73401730
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401732
feature_type: variation
id: rs2063028320
seq_region_name: 17
source: dbSNP
start: 73401732
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401737
feature_type: variation
id: rs1337337086
seq_region_name: 17
source: dbSNP
start: 73401737
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401739
feature_type: variation
id: rs943720829
seq_region_name: 17
source: dbSNP
start: 73401739
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401741
feature_type: variation
id: rs2063028432
seq_region_name: 17
source: dbSNP
start: 73401741
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401742
feature_type: variation
id: rs768734909
seq_region_name: 17
source: dbSNP
start: 73401742
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401745
feature_type: variation
id: rs1808695181
seq_region_name: 17
source: dbSNP
start: 73401745
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401747
feature_type: variation
id: rs1279056692
seq_region_name: 17
source: dbSNP
start: 73401747
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401750
feature_type: variation
id: rs2063028546
seq_region_name: 17
source: dbSNP
start: 73401750
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401755
feature_type: variation
id: rs1313802307
seq_region_name: 17
source: dbSNP
start: 73401755
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401756
feature_type: variation
id: rs374102014
seq_region_name: 17
source: dbSNP
start: 73401756
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401758
feature_type: variation
id: rs897046352
seq_region_name: 17
source: dbSNP
start: 73401758
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401759
feature_type: variation
id: rs1242157841
seq_region_name: 17
source: dbSNP
start: 73401759
strand: 1
-
alleles:
- AAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401765
feature_type: variation
id: rs1464915525
seq_region_name: 17
source: dbSNP
start: 73401762
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401763
feature_type: variation
id: rs973383321
seq_region_name: 17
source: dbSNP
start: 73401763
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401764
feature_type: variation
id: rs1280007063
seq_region_name: 17
source: dbSNP
start: 73401764
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73401769
feature_type: variation
id: rs2063028718
seq_region_name: 17
source: dbSNP
start: 73401769
strand: 1
-
alleles:
- ACCCCCACCCCC
- ACCCCCACCCCCACCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401780
feature_type: variation
id: rs1555761672
seq_region_name: 17
source: dbSNP
start: 73401769
strand: 1
-
alleles:
- CCCCC
- CCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401774
feature_type: variation
id: rs1189973108
seq_region_name: 17
source: dbSNP
start: 73401770
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401771
feature_type: variation
id: rs2145528150
seq_region_name: 17
source: dbSNP
start: 73401771
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401773
feature_type: variation
id: rs770144139
seq_region_name: 17
source: dbSNP
start: 73401773
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401774
feature_type: variation
id: rs1474700555
seq_region_name: 17
source: dbSNP
start: 73401774
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401775
feature_type: variation
id: rs1599528256
seq_region_name: 17
source: dbSNP
start: 73401775
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401776
feature_type: variation
id: rs527728344
seq_region_name: 17
source: dbSNP
start: 73401776
strand: 1
-
alleles:
- CCCCCC
- CCCCC
- CCCCCCC
- CCCCCCCC
- CCCCCCCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401781
feature_type: variation
id: rs140071991
seq_region_name: 17
source: dbSNP
start: 73401776
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401777
feature_type: variation
id: rs927372739
seq_region_name: 17
source: dbSNP
start: 73401777
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401778
feature_type: variation
id: rs1400425898
seq_region_name: 17
source: dbSNP
start: 73401778
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401779
feature_type: variation
id: rs1386335901
seq_region_name: 17
source: dbSNP
start: 73401779
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401779
feature_type: variation
id: rs1471169134
seq_region_name: 17
source: dbSNP
start: 73401780
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401780
feature_type: variation
id: rs778643740
seq_region_name: 17
source: dbSNP
start: 73401780
strand: 1
-
alleles:
- "-"
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401780
feature_type: variation
id: rs200470291
seq_region_name: 17
source: dbSNP
start: 73401781
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401781
feature_type: variation
id: rs771628255
seq_region_name: 17
source: dbSNP
start: 73401781
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401783
feature_type: variation
id: rs1405662990
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1284685938
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs79476391
seq_region_name: 17
source: dbSNP
start: 73401822
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1357541089
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063029545
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source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063029570
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063029600
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source: dbSNP
start: 73401840
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs1237609977
seq_region_name: 17
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start: 73401842
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs905735628
seq_region_name: 17
source: dbSNP
start: 73401846
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063029719
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1291155651
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- AGCCTGGGCCACCCTTCTGCCTGGGGCGCCCAGCCTGG
- AGCCTGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063029784
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- G
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401872
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145528496
seq_region_name: 17
source: dbSNP
start: 73401874
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401875
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs567259047
seq_region_name: 17
source: dbSNP
start: 73401878
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1381627489
seq_region_name: 17
source: dbSNP
start: 73401882
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
start: 73401889
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73401890
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063030059
seq_region_name: 17
source: dbSNP
start: 73401891
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs186481586
seq_region_name: 17
source: dbSNP
start: 73401892
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401895
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401896
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401897
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73401899
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73401900
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401903
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73401905
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73401907
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401907
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73401908
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73401908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73401908
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs752909976
seq_region_name: 17
source: dbSNP
start: 73401909
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs371867380
seq_region_name: 17
source: dbSNP
start: 73401909
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs201295692
seq_region_name: 17
source: dbSNP
start: 73401910
strand: 1
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alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1018642143
seq_region_name: 17
source: dbSNP
start: 73401911
strand: 1
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alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs538444048
seq_region_name: 17
source: dbSNP
start: 73401911
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs76839449
seq_region_name: 17
source: dbSNP
start: 73401912
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs778272183
seq_region_name: 17
source: dbSNP
start: 73401913
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs774959685
seq_region_name: 17
source: dbSNP
start: 73401914
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401914
feature_type: variation
id: rs756268897
seq_region_name: 17
source: dbSNP
start: 73401915
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs759984791
seq_region_name: 17
source: dbSNP
start: 73401915
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1438639861
seq_region_name: 17
source: dbSNP
start: 73401916
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401916
feature_type: variation
id: rs774865150
seq_region_name: 17
source: dbSNP
start: 73401916
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401917
feature_type: variation
id: rs763793286
seq_region_name: 17
source: dbSNP
start: 73401917
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401919
feature_type: variation
id: rs1197670255
seq_region_name: 17
source: dbSNP
start: 73401919
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401922
feature_type: variation
id: rs1429081448
seq_region_name: 17
source: dbSNP
start: 73401922
strand: 1
-
alleles:
- AGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401925
feature_type: variation
id: rs2063030962
seq_region_name: 17
source: dbSNP
start: 73401922
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401923
feature_type: variation
id: rs1323356524
seq_region_name: 17
source: dbSNP
start: 73401923
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401926
feature_type: variation
id: rs753603631
seq_region_name: 17
source: dbSNP
start: 73401926
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401930
feature_type: variation
id: rs1160577248
seq_region_name: 17
source: dbSNP
start: 73401930
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401931
feature_type: variation
id: rs1400400459
seq_region_name: 17
source: dbSNP
start: 73401931
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401933
feature_type: variation
id: rs761636684
seq_region_name: 17
source: dbSNP
start: 73401933
strand: 1
-
alleles:
- GGGGGG
- GGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73401938
feature_type: variation
id: rs777783482
seq_region_name: 17
source: dbSNP
start: 73401933
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401934
feature_type: variation
id: rs1568384039
seq_region_name: 17
source: dbSNP
start: 73401934
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401935
feature_type: variation
id: rs1324074922
seq_region_name: 17
source: dbSNP
start: 73401935
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401936
feature_type: variation
id: rs1029077715
seq_region_name: 17
source: dbSNP
start: 73401936
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73401937
feature_type: variation
id: rs372946925
seq_region_name: 17
source: dbSNP
start: 73401937
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73401940
feature_type: variation
id: rs2063031189
seq_region_name: 17
source: dbSNP
start: 73401940
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73401942
feature_type: variation
id: rs1282373704
seq_region_name: 17
source: dbSNP
start: 73401942
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401946
feature_type: variation
id: rs917803816
seq_region_name: 17
source: dbSNP
start: 73401946
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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feature_type: variation
id: rs750310836
seq_region_name: 17
source: dbSNP
start: 73401948
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401949
feature_type: variation
id: rs758280017
seq_region_name: 17
source: dbSNP
start: 73401949
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401954
feature_type: variation
id: rs2063031320
seq_region_name: 17
source: dbSNP
start: 73401954
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401957
feature_type: variation
id: rs767632454
seq_region_name: 17
source: dbSNP
start: 73401957
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401959
feature_type: variation
id: rs1349272843
seq_region_name: 17
source: dbSNP
start: 73401959
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401960
feature_type: variation
id: rs1209942892
seq_region_name: 17
source: dbSNP
start: 73401960
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401961
feature_type: variation
id: rs752779529
seq_region_name: 17
source: dbSNP
start: 73401961
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401965
feature_type: variation
id: rs2063031488
seq_region_name: 17
source: dbSNP
start: 73401965
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401970
feature_type: variation
id: rs756338701
seq_region_name: 17
source: dbSNP
start: 73401970
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401971
feature_type: variation
id: rs367637254
seq_region_name: 17
source: dbSNP
start: 73401971
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73401971
feature_type: variation
id: rs2063031579
seq_region_name: 17
source: dbSNP
start: 73401971
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401972
feature_type: variation
id: rs749556489
seq_region_name: 17
source: dbSNP
start: 73401972
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401975
feature_type: variation
id: rs2063031649
seq_region_name: 17
source: dbSNP
start: 73401975
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401976
feature_type: variation
id: rs1599528622
seq_region_name: 17
source: dbSNP
start: 73401976
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401977
feature_type: variation
id: rs1266040433
seq_region_name: 17
source: dbSNP
start: 73401977
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401981
feature_type: variation
id: rs757650185
seq_region_name: 17
source: dbSNP
start: 73401981
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401982
feature_type: variation
id: rs1420059012
seq_region_name: 17
source: dbSNP
start: 73401982
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401986
feature_type: variation
id: rs1184184253
seq_region_name: 17
source: dbSNP
start: 73401986
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401987
feature_type: variation
id: rs866508685
seq_region_name: 17
source: dbSNP
start: 73401987
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401989
feature_type: variation
id: rs1362307292
seq_region_name: 17
source: dbSNP
start: 73401989
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401991
feature_type: variation
id: rs2063031826
seq_region_name: 17
source: dbSNP
start: 73401991
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73401993
feature_type: variation
id: rs779436125
seq_region_name: 17
source: dbSNP
start: 73401993
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73401995
feature_type: variation
id: rs746322137
seq_region_name: 17
source: dbSNP
start: 73401995
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73401999
feature_type: variation
id: rs772519437
seq_region_name: 17
source: dbSNP
start: 73401999
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402000
feature_type: variation
id: rs1599528666
seq_region_name: 17
source: dbSNP
start: 73402000
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402016
feature_type: variation
id: rs775048572
seq_region_name: 17
source: dbSNP
start: 73402016
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73402017
feature_type: variation
id: rs2063032015
seq_region_name: 17
source: dbSNP
start: 73402017
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402018
feature_type: variation
id: rs2145529210
seq_region_name: 17
source: dbSNP
start: 73402018
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402019
feature_type: variation
id: rs746546033
seq_region_name: 17
source: dbSNP
start: 73402019
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402021
feature_type: variation
id: rs1370876715
seq_region_name: 17
source: dbSNP
start: 73402021
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402022
feature_type: variation
id: rs1392940362
seq_region_name: 17
source: dbSNP
start: 73402022
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402031
feature_type: variation
id: rs9302962
seq_region_name: 17
source: dbSNP
start: 73402031
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402034
feature_type: variation
id: rs925274428
seq_region_name: 17
source: dbSNP
start: 73402034
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402036
feature_type: variation
id: rs776225115
seq_region_name: 17
source: dbSNP
start: 73402036
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402039
feature_type: variation
id: rs1316516090
seq_region_name: 17
source: dbSNP
start: 73402039
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402045
feature_type: variation
id: rs146601014
seq_region_name: 17
source: dbSNP
start: 73402045
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402047
feature_type: variation
id: rs536286755
seq_region_name: 17
source: dbSNP
start: 73402047
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402049
feature_type: variation
id: rs1568384123
seq_region_name: 17
source: dbSNP
start: 73402049
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402050
feature_type: variation
id: rs1461019493
seq_region_name: 17
source: dbSNP
start: 73402050
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402053
feature_type: variation
id: rs1291714970
seq_region_name: 17
source: dbSNP
start: 73402053
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402054
feature_type: variation
id: rs772950192
seq_region_name: 17
source: dbSNP
start: 73402054
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402055
feature_type: variation
id: rs766276467
seq_region_name: 17
source: dbSNP
start: 73402055
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402058
feature_type: variation
id: rs2063032528
seq_region_name: 17
source: dbSNP
start: 73402058
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402059
feature_type: variation
id: rs1416308418
seq_region_name: 17
source: dbSNP
start: 73402059
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402063
feature_type: variation
id: rs752790641
seq_region_name: 17
source: dbSNP
start: 73402063
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402064
feature_type: variation
id: rs777255747
seq_region_name: 17
source: dbSNP
start: 73402064
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402070
feature_type: variation
id: rs554618657
seq_region_name: 17
source: dbSNP
start: 73402070
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402072
feature_type: variation
id: rs757560189
seq_region_name: 17
source: dbSNP
start: 73402072
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402076
feature_type: variation
id: rs1450075341
seq_region_name: 17
source: dbSNP
start: 73402076
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402077
feature_type: variation
id: rs972798671
seq_region_name: 17
source: dbSNP
start: 73402077
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402078
feature_type: variation
id: rs779413970
seq_region_name: 17
source: dbSNP
start: 73402078
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402079
feature_type: variation
id: rs746273973
seq_region_name: 17
source: dbSNP
start: 73402079
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402086
feature_type: variation
id: rs2063032878
seq_region_name: 17
source: dbSNP
start: 73402086
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402089
feature_type: variation
id: rs758913644
seq_region_name: 17
source: dbSNP
start: 73402089
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402090
feature_type: variation
id: rs780461665
seq_region_name: 17
source: dbSNP
start: 73402090
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402091
feature_type: variation
id: rs1296215447
seq_region_name: 17
source: dbSNP
start: 73402091
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402092
feature_type: variation
id: rs768105886
seq_region_name: 17
source: dbSNP
start: 73402092
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402093
feature_type: variation
id: rs776130067
seq_region_name: 17
source: dbSNP
start: 73402093
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402094
feature_type: variation
id: rs931222989
seq_region_name: 17
source: dbSNP
start: 73402094
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402099
feature_type: variation
id: rs769496398
seq_region_name: 17
source: dbSNP
start: 73402099
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402100
feature_type: variation
id: rs1048312397
seq_region_name: 17
source: dbSNP
start: 73402100
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402102
feature_type: variation
id: rs773038864
seq_region_name: 17
source: dbSNP
start: 73402102
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402103
feature_type: variation
id: rs927080427
seq_region_name: 17
source: dbSNP
start: 73402103
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402105
feature_type: variation
id: rs762696400
seq_region_name: 17
source: dbSNP
start: 73402105
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402108
feature_type: variation
id: rs766228245
seq_region_name: 17
source: dbSNP
start: 73402108
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402109
feature_type: variation
id: rs1308569923
seq_region_name: 17
source: dbSNP
start: 73402109
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402110
feature_type: variation
id: rs370278678
seq_region_name: 17
source: dbSNP
start: 73402110
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402112
feature_type: variation
id: rs754040424
seq_region_name: 17
source: dbSNP
start: 73402112
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402113
feature_type: variation
id: rs2063033422
seq_region_name: 17
source: dbSNP
start: 73402113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402114
feature_type: variation
id: rs2063033468
seq_region_name: 17
source: dbSNP
start: 73402114
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402120
feature_type: variation
id: rs2063033519
seq_region_name: 17
source: dbSNP
start: 73402120
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402124
feature_type: variation
id: rs762110670
seq_region_name: 17
source: dbSNP
start: 73402124
strand: 1
-
alleles:
- CGGC
- CGGCGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_insertion
end: 73402127
feature_type: variation
id: rs2063033624
seq_region_name: 17
source: dbSNP
start: 73402124
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402125
feature_type: variation
id: rs1599528890
seq_region_name: 17
source: dbSNP
start: 73402125
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73402133
feature_type: variation
id: rs765423400
seq_region_name: 17
source: dbSNP
start: 73402133
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402134
feature_type: variation
id: rs576079011
seq_region_name: 17
source: dbSNP
start: 73402134
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402135
feature_type: variation
id: rs750764539
seq_region_name: 17
source: dbSNP
start: 73402135
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73402136
feature_type: variation
id: rs139222271
seq_region_name: 17
source: dbSNP
start: 73402136
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402137
feature_type: variation
id: rs374610597
seq_region_name: 17
source: dbSNP
start: 73402137
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73402138
feature_type: variation
id: rs2145529875
seq_region_name: 17
source: dbSNP
start: 73402138
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73402144
feature_type: variation
id: rs780669050
seq_region_name: 17
source: dbSNP
start: 73402144
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73402145
feature_type: variation
id: rs769406571
seq_region_name: 17
source: dbSNP
start: 73402145
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73402146
feature_type: variation
id: rs2063034074
seq_region_name: 17
source: dbSNP
start: 73402146
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73402149
feature_type: variation
id: rs748995927
seq_region_name: 17
source: dbSNP
start: 73402149
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73402153
feature_type: variation
id: rs1372219929
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source: dbSNP
start: 73402153
strand: 1
-
alleles:
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- C
- T
assembly_name: GRCh38
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consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs1470132866
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063034242
seq_region_name: 17
source: dbSNP
start: 73402165
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs772190750
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145529963
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1320616053
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063034320
seq_region_name: 17
source: dbSNP
start: 73402172
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs776827254
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1381592716
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1384416267
seq_region_name: 17
source: dbSNP
start: 73402175
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1313060744
seq_region_name: 17
source: dbSNP
start: 73402179
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1005905057
seq_region_name: 17
source: dbSNP
start: 73402181
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402183
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1326164801
seq_region_name: 17
source: dbSNP
start: 73402184
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs372289510
seq_region_name: 17
source: dbSNP
start: 73402188
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1400557836
seq_region_name: 17
source: dbSNP
start: 73402190
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1265430965
seq_region_name: 17
source: dbSNP
start: 73402191
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs750058718
seq_region_name: 17
source: dbSNP
start: 73402194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1161751157
seq_region_name: 17
source: dbSNP
start: 73402195
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063034603
seq_region_name: 17
source: dbSNP
start: 73402196
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1010353272
seq_region_name: 17
source: dbSNP
start: 73402201
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs142576395
seq_region_name: 17
source: dbSNP
start: 73402205
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs530289357
seq_region_name: 17
source: dbSNP
start: 73402211
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs563000067
seq_region_name: 17
source: dbSNP
start: 73402212
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063034706
seq_region_name: 17
source: dbSNP
start: 73402214
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063034725
seq_region_name: 17
source: dbSNP
start: 73402217
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1261536330
seq_region_name: 17
source: dbSNP
start: 73402228
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1025221176
seq_region_name: 17
source: dbSNP
start: 73402231
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1489575995
seq_region_name: 17
source: dbSNP
start: 73402232
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599529028
seq_region_name: 17
source: dbSNP
start: 73402233
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063034844
seq_region_name: 17
source: dbSNP
start: 73402234
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1267303641
seq_region_name: 17
source: dbSNP
start: 73402235
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1000821400
seq_region_name: 17
source: dbSNP
start: 73402238
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1029213474
seq_region_name: 17
source: dbSNP
start: 73402239
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402242
feature_type: variation
id: rs1265484253
seq_region_name: 17
source: dbSNP
start: 73402242
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs182804286
seq_region_name: 17
source: dbSNP
start: 73402244
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs371291663
seq_region_name: 17
source: dbSNP
start: 73402245
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063034968
seq_region_name: 17
source: dbSNP
start: 73402249
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs76809473
seq_region_name: 17
source: dbSNP
start: 73402251
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402254
feature_type: variation
id: rs958001339
seq_region_name: 17
source: dbSNP
start: 73402254
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402257
feature_type: variation
id: rs1599529059
seq_region_name: 17
source: dbSNP
start: 73402257
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402258
feature_type: variation
id: rs1218940415
seq_region_name: 17
source: dbSNP
start: 73402258
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402263
feature_type: variation
id: rs1355267683
seq_region_name: 17
source: dbSNP
start: 73402263
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402267
feature_type: variation
id: rs1301284957
seq_region_name: 17
source: dbSNP
start: 73402267
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402268
feature_type: variation
id: rs2063035125
seq_region_name: 17
source: dbSNP
start: 73402268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402275
feature_type: variation
id: rs2063035148
seq_region_name: 17
source: dbSNP
start: 73402275
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402277
feature_type: variation
id: rs2145530347
seq_region_name: 17
source: dbSNP
start: 73402277
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402281
feature_type: variation
id: rs1463733746
seq_region_name: 17
source: dbSNP
start: 73402281
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402285
feature_type: variation
id: rs1391598061
seq_region_name: 17
source: dbSNP
start: 73402285
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402286
feature_type: variation
id: rs2145530370
seq_region_name: 17
source: dbSNP
start: 73402286
strand: 1
-
alleles:
- AA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402294
feature_type: variation
id: rs1295342564
seq_region_name: 17
source: dbSNP
start: 73402293
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402295
feature_type: variation
id: rs2063035225
seq_region_name: 17
source: dbSNP
start: 73402295
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402299
feature_type: variation
id: rs1008996323
seq_region_name: 17
source: dbSNP
start: 73402299
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402300
feature_type: variation
id: rs1019083126
seq_region_name: 17
source: dbSNP
start: 73402300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402304
feature_type: variation
id: rs1599529098
seq_region_name: 17
source: dbSNP
start: 73402304
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402305
feature_type: variation
id: rs560241624
seq_region_name: 17
source: dbSNP
start: 73402305
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402306
feature_type: variation
id: rs113303998
seq_region_name: 17
source: dbSNP
start: 73402306
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402307
feature_type: variation
id: rs2145530433
seq_region_name: 17
source: dbSNP
start: 73402307
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402310
feature_type: variation
id: rs1478974379
seq_region_name: 17
source: dbSNP
start: 73402310
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402311
feature_type: variation
id: rs2063035395
seq_region_name: 17
source: dbSNP
start: 73402311
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402314
feature_type: variation
id: rs1427632822
seq_region_name: 17
source: dbSNP
start: 73402314
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402318
feature_type: variation
id: rs527766825
seq_region_name: 17
source: dbSNP
start: 73402318
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402322
feature_type: variation
id: rs2063035490
seq_region_name: 17
source: dbSNP
start: 73402322
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402324
feature_type: variation
id: rs944116656
seq_region_name: 17
source: dbSNP
start: 73402324
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402325
feature_type: variation
id: rs549034068
seq_region_name: 17
source: dbSNP
start: 73402325
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402331
feature_type: variation
id: rs918735092
seq_region_name: 17
source: dbSNP
start: 73402331
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402334
feature_type: variation
id: rs2063035592
seq_region_name: 17
source: dbSNP
start: 73402334
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402337
feature_type: variation
id: rs2063035628
seq_region_name: 17
source: dbSNP
start: 73402337
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402338
feature_type: variation
id: rs2063035663
seq_region_name: 17
source: dbSNP
start: 73402338
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402339
feature_type: variation
id: rs1256961203
seq_region_name: 17
source: dbSNP
start: 73402339
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402344
feature_type: variation
id: rs2063035700
seq_region_name: 17
source: dbSNP
start: 73402344
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402345
feature_type: variation
id: rs2063035746
seq_region_name: 17
source: dbSNP
start: 73402345
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402347
feature_type: variation
id: rs2063035779
seq_region_name: 17
source: dbSNP
start: 73402347
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402348
feature_type: variation
id: rs79723673
seq_region_name: 17
source: dbSNP
start: 73402348
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402349
feature_type: variation
id: rs1198864867
seq_region_name: 17
source: dbSNP
start: 73402349
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402350
feature_type: variation
id: rs2063035865
seq_region_name: 17
source: dbSNP
start: 73402350
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402353
feature_type: variation
id: rs918243317
seq_region_name: 17
source: dbSNP
start: 73402353
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402357
feature_type: variation
id: rs2063035911
seq_region_name: 17
source: dbSNP
start: 73402357
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402358
feature_type: variation
id: rs930180909
seq_region_name: 17
source: dbSNP
start: 73402358
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402365
feature_type: variation
id: rs1568384340
seq_region_name: 17
source: dbSNP
start: 73402365
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402366
feature_type: variation
id: rs1232508238
seq_region_name: 17
source: dbSNP
start: 73402366
strand: 1
-
alleles:
- GTG
- GTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402368
feature_type: variation
id: rs2063036044
seq_region_name: 17
source: dbSNP
start: 73402366
strand: 1
-
alleles:
- "-"
- AGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402371
feature_type: variation
id: rs199585941
seq_region_name: 17
source: dbSNP
start: 73402372
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402372
feature_type: variation
id: rs2145530637
seq_region_name: 17
source: dbSNP
start: 73402372
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73402543
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73402548
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73402552
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73402556
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402582
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73402588
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73402591
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402593
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73402594
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063037884
seq_region_name: 17
source: dbSNP
start: 73402596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2145531346
seq_region_name: 17
source: dbSNP
start: 73402598
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145531367
seq_region_name: 17
source: dbSNP
start: 73402599
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2145531382
seq_region_name: 17
source: dbSNP
start: 73402600
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063037909
seq_region_name: 17
source: dbSNP
start: 73402600
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs889336662
seq_region_name: 17
source: dbSNP
start: 73402602
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs770146810
seq_region_name: 17
source: dbSNP
start: 73402603
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402606
feature_type: variation
id: rs1327674321
seq_region_name: 17
source: dbSNP
start: 73402606
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402608
feature_type: variation
id: rs1056088058
seq_region_name: 17
source: dbSNP
start: 73402608
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402611
feature_type: variation
id: rs1440104602
seq_region_name: 17
source: dbSNP
start: 73402611
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1357568133
seq_region_name: 17
source: dbSNP
start: 73402615
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402616
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id: rs1342680656
seq_region_name: 17
source: dbSNP
start: 73402616
strand: 1
-
alleles:
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- TT
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assembly_name: GRCh38
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strand: 1
-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402662
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402663
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402685
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402689
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063038501
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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id: rs1218683039
seq_region_name: 17
source: dbSNP
start: 73402704
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402705
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402710
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402716
strand: 1
-
alleles:
- CTCAGCCTCCCAA
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145531783
seq_region_name: 17
source: dbSNP
start: 73402721
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402739
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73402749
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73402751
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402753
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402755
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402756
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063038878
seq_region_name: 17
source: dbSNP
start: 73402757
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs575848236
seq_region_name: 17
source: dbSNP
start: 73402758
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402760
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1333267939
seq_region_name: 17
source: dbSNP
start: 73402764
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1403635230
seq_region_name: 17
source: dbSNP
start: 73402765
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402766
feature_type: variation
id: rs1025417982
seq_region_name: 17
source: dbSNP
start: 73402766
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402768
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402772
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402774
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063039070
seq_region_name: 17
source: dbSNP
start: 73402776
strand: 1
-
alleles:
- TATTTTATTTTATT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1347653540
seq_region_name: 17
source: dbSNP
start: 73402777
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs187485825
seq_region_name: 17
source: dbSNP
start: 73402781
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs983761150
seq_region_name: 17
source: dbSNP
start: 73402783
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402785
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402788
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs951441987
seq_region_name: 17
source: dbSNP
start: 73402789
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1195806621
seq_region_name: 17
source: dbSNP
start: 73402791
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063039308
seq_region_name: 17
source: dbSNP
start: 73402793
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402796
feature_type: variation
id: rs2063039336
seq_region_name: 17
source: dbSNP
start: 73402796
strand: 1
-
alleles:
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- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402802
feature_type: variation
id: rs1246226483
seq_region_name: 17
source: dbSNP
start: 73402796
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402797
feature_type: variation
id: rs536372857
seq_region_name: 17
source: dbSNP
start: 73402797
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402800
feature_type: variation
id: rs1453549649
seq_region_name: 17
source: dbSNP
start: 73402800
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402814
feature_type: variation
id: rs984240442
seq_region_name: 17
source: dbSNP
start: 73402800
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402805
feature_type: variation
id: rs1271078122
seq_region_name: 17
source: dbSNP
start: 73402805
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402810
feature_type: variation
id: rs2063039471
seq_region_name: 17
source: dbSNP
start: 73402810
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402815
feature_type: variation
id: rs958573515
seq_region_name: 17
source: dbSNP
start: 73402815
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402816
feature_type: variation
id: rs2063039513
seq_region_name: 17
source: dbSNP
start: 73402816
strand: 1
-
alleles:
- ACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402821
feature_type: variation
id: rs2063039536
seq_region_name: 17
source: dbSNP
start: 73402819
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402820
feature_type: variation
id: rs2063039565
seq_region_name: 17
source: dbSNP
start: 73402820
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402821
feature_type: variation
id: rs554657946
seq_region_name: 17
source: dbSNP
start: 73402821
strand: 1
-
alleles:
- AGAG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402824
feature_type: variation
id: rs2063039612
seq_region_name: 17
source: dbSNP
start: 73402821
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402821
feature_type: variation
id: rs2063039641
seq_region_name: 17
source: dbSNP
start: 73402822
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402822
feature_type: variation
id: rs763180686
seq_region_name: 17
source: dbSNP
start: 73402822
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402824
feature_type: variation
id: rs2063039714
seq_region_name: 17
source: dbSNP
start: 73402824
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402827
feature_type: variation
id: rs2063039743
seq_region_name: 17
source: dbSNP
start: 73402825
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402826
feature_type: variation
id: rs2063039775
seq_region_name: 17
source: dbSNP
start: 73402826
strand: 1
-
alleles:
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- CTTACTTACTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402832
feature_type: variation
id: rs2063039802
seq_region_name: 17
source: dbSNP
start: 73402826
strand: 1
-
alleles:
- TTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402833
feature_type: variation
id: rs2063039827
seq_region_name: 17
source: dbSNP
start: 73402831
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402834
feature_type: variation
id: rs2063039853
seq_region_name: 17
source: dbSNP
start: 73402834
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402836
feature_type: variation
id: rs917062349
seq_region_name: 17
source: dbSNP
start: 73402836
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402837
feature_type: variation
id: rs569678392
seq_region_name: 17
source: dbSNP
start: 73402837
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402841
feature_type: variation
id: rs536634560
seq_region_name: 17
source: dbSNP
start: 73402841
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402847
feature_type: variation
id: rs2145532303
seq_region_name: 17
source: dbSNP
start: 73402847
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402848
feature_type: variation
id: rs764347909
seq_region_name: 17
source: dbSNP
start: 73402848
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402852
feature_type: variation
id: rs977889666
seq_region_name: 17
source: dbSNP
start: 73402852
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73402853
feature_type: variation
id: rs2063039990
seq_region_name: 17
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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- G
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73402907
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063040745
seq_region_name: 17
source: dbSNP
start: 73402916
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs902224781
seq_region_name: 17
source: dbSNP
start: 73402927
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1355638891
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063040841
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402938
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402942
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
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id: rs897973282
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402962
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
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id: rs542719005
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- TTTTT
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063041302
seq_region_name: 17
source: dbSNP
start: 73402970
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063041324
seq_region_name: 17
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063041357
seq_region_name: 17
source: dbSNP
start: 73402981
strand: 1
-
alleles:
- GGGGG
- GGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063041388
seq_region_name: 17
source: dbSNP
start: 73402987
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs888170569
seq_region_name: 17
source: dbSNP
start: 73402990
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73402991
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402997
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73402998
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73402999
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73403000
strand: 1
-
alleles:
- TGGCCAGGCTGGTCTCGAACTCCTG
- TGGCCAGGCTGGTCTCGAACTCCTGGCCAGGCTGGTCTCGAACTCCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403027
feature_type: variation
id: rs2145532852
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403007
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403008
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73403010
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403011
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs531775596
seq_region_name: 17
source: dbSNP
start: 73403013
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063041598
seq_region_name: 17
source: dbSNP
start: 73403014
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1486096143
seq_region_name: 17
source: dbSNP
start: 73403018
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403019
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1212915584
seq_region_name: 17
source: dbSNP
start: 73403020
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1315600010
seq_region_name: 17
source: dbSNP
start: 73403021
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063041719
seq_region_name: 17
source: dbSNP
start: 73403022
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145532997
seq_region_name: 17
source: dbSNP
start: 73403024
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1190376352
seq_region_name: 17
source: dbSNP
start: 73403027
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs372969204
seq_region_name: 17
source: dbSNP
start: 73403029
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403038
feature_type: variation
id: rs967717137
seq_region_name: 17
source: dbSNP
start: 73403038
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403040
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403041
feature_type: variation
id: rs977252123
seq_region_name: 17
source: dbSNP
start: 73403041
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1378226296
seq_region_name: 17
source: dbSNP
start: 73403042
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403045
feature_type: variation
id: rs148274071
seq_region_name: 17
source: dbSNP
start: 73403045
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs141386812
seq_region_name: 17
source: dbSNP
start: 73403046
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867269761
seq_region_name: 17
source: dbSNP
start: 73403050
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403051
feature_type: variation
id: rs184129056
seq_region_name: 17
source: dbSNP
start: 73403051
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403052
feature_type: variation
id: rs112096909
seq_region_name: 17
source: dbSNP
start: 73403052
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403059
feature_type: variation
id: rs2063042109
seq_region_name: 17
source: dbSNP
start: 73403059
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403061
feature_type: variation
id: rs1310749862
seq_region_name: 17
source: dbSNP
start: 73403061
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403066
feature_type: variation
id: rs2063042169
seq_region_name: 17
source: dbSNP
start: 73403066
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403067
feature_type: variation
id: rs2063042195
seq_region_name: 17
source: dbSNP
start: 73403067
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403071
feature_type: variation
id: rs376088401
seq_region_name: 17
source: dbSNP
start: 73403071
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403077
feature_type: variation
id: rs1040798415
seq_region_name: 17
source: dbSNP
start: 73403077
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403078
feature_type: variation
id: rs1599529837
seq_region_name: 17
source: dbSNP
start: 73403078
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403079
feature_type: variation
id: rs1415002187
seq_region_name: 17
source: dbSNP
start: 73403079
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403084
feature_type: variation
id: rs1447670262
seq_region_name: 17
source: dbSNP
start: 73403084
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403085
feature_type: variation
id: rs565885197
seq_region_name: 17
source: dbSNP
start: 73403085
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403086
feature_type: variation
id: rs929557533
seq_region_name: 17
source: dbSNP
start: 73403086
strand: 1
-
alleles:
- C
- G
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73403197
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73403202
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73403207
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73403210
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403211
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403224
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403226
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73403232
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73403234
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403239
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73403240
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73403245
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73403249
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403251
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403258
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403259
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs915001547
seq_region_name: 17
source: dbSNP
start: 73403261
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403272
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063043920
seq_region_name: 17
source: dbSNP
start: 73403277
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063043944
seq_region_name: 17
source: dbSNP
start: 73403279
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403287
feature_type: variation
id: rs2063043970
seq_region_name: 17
source: dbSNP
start: 73403282
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063043994
seq_region_name: 17
source: dbSNP
start: 73403284
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403285
feature_type: variation
id: rs1368383557
seq_region_name: 17
source: dbSNP
start: 73403285
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1295581457
seq_region_name: 17
source: dbSNP
start: 73403286
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403291
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id: rs2063044058
seq_region_name: 17
source: dbSNP
start: 73403291
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063044077
seq_region_name: 17
source: dbSNP
start: 73403293
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403298
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403298
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403299
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063044155
seq_region_name: 17
source: dbSNP
start: 73403300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403308
feature_type: variation
id: rs2063044201
seq_region_name: 17
source: dbSNP
start: 73403304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1455240373
seq_region_name: 17
source: dbSNP
start: 73403305
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1171776209
seq_region_name: 17
source: dbSNP
start: 73403306
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73403309
feature_type: variation
id: rs1467674409
seq_region_name: 17
source: dbSNP
start: 73403309
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063044338
seq_region_name: 17
source: dbSNP
start: 73403311
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403313
feature_type: variation
id: rs986163418
seq_region_name: 17
source: dbSNP
start: 73403313
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
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end: 73403316
feature_type: variation
id: rs2063044438
seq_region_name: 17
source: dbSNP
start: 73403316
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403317
feature_type: variation
id: rs910658026
seq_region_name: 17
source: dbSNP
start: 73403317
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403321
feature_type: variation
id: rs1410205081
seq_region_name: 17
source: dbSNP
start: 73403321
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403322
feature_type: variation
id: rs966114262
seq_region_name: 17
source: dbSNP
start: 73403322
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403325
feature_type: variation
id: rs2063044542
seq_region_name: 17
source: dbSNP
start: 73403325
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403328
feature_type: variation
id: rs2145533858
seq_region_name: 17
source: dbSNP
start: 73403328
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403333
feature_type: variation
id: rs901037970
seq_region_name: 17
source: dbSNP
start: 73403333
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403337
feature_type: variation
id: rs1356680554
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs887084518
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1331798357
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599530099
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1303471620
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1371809641
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- GTTCTTG
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063045298
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1278677187
seq_region_name: 17
source: dbSNP
start: 73403395
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1344525651
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
id: rs367875753
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145534179
seq_region_name: 17
source: dbSNP
start: 73403418
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1055319470
seq_region_name: 17
source: dbSNP
start: 73403420
strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs200637447
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs894201909
seq_region_name: 17
source: dbSNP
start: 73403421
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1024468052
seq_region_name: 17
source: dbSNP
start: 73403424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1020152217
seq_region_name: 17
source: dbSNP
start: 73403425
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs1014428325
seq_region_name: 17
source: dbSNP
start: 73403426
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1345574711
seq_region_name: 17
source: dbSNP
start: 73403426
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1237970028
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1045363535
seq_region_name: 17
source: dbSNP
start: 73403428
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063045762
seq_region_name: 17
source: dbSNP
start: 73403430
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1469775453
seq_region_name: 17
source: dbSNP
start: 73403431
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063045845
seq_region_name: 17
source: dbSNP
start: 73403434
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs902884921
seq_region_name: 17
source: dbSNP
start: 73403435
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403438
feature_type: variation
id: rs2145534319
seq_region_name: 17
source: dbSNP
start: 73403438
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599530191
seq_region_name: 17
source: dbSNP
start: 73403440
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599530195
seq_region_name: 17
source: dbSNP
start: 73403441
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs192735433
seq_region_name: 17
source: dbSNP
start: 73403443
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs572317473
seq_region_name: 17
source: dbSNP
start: 73403444
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063046017
seq_region_name: 17
source: dbSNP
start: 73403448
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403450
feature_type: variation
id: rs2063046037
seq_region_name: 17
source: dbSNP
start: 73403450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1397155239
seq_region_name: 17
source: dbSNP
start: 73403452
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1475517213
seq_region_name: 17
source: dbSNP
start: 73403453
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403456
feature_type: variation
id: rs1169334899
seq_region_name: 17
source: dbSNP
start: 73403456
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063046136
seq_region_name: 17
source: dbSNP
start: 73403462
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs977681059
seq_region_name: 17
source: dbSNP
start: 73403463
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs777552931
seq_region_name: 17
source: dbSNP
start: 73403464
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1158916891
seq_region_name: 17
source: dbSNP
start: 73403465
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063046221
seq_region_name: 17
source: dbSNP
start: 73403467
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403468
feature_type: variation
id: rs956342160
seq_region_name: 17
source: dbSNP
start: 73403468
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1366525976
seq_region_name: 17
source: dbSNP
start: 73403469
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403469
feature_type: variation
id: rs2063046244
seq_region_name: 17
source: dbSNP
start: 73403469
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403477
feature_type: variation
id: rs1599530242
seq_region_name: 17
source: dbSNP
start: 73403477
strand: 1
-
alleles:
- C
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403479
feature_type: variation
id: rs1186534966
seq_region_name: 17
source: dbSNP
start: 73403479
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403484
feature_type: variation
id: rs2063046349
seq_region_name: 17
source: dbSNP
start: 73403484
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403485
feature_type: variation
id: rs542807179
seq_region_name: 17
source: dbSNP
start: 73403485
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403488
feature_type: variation
id: rs2063046398
seq_region_name: 17
source: dbSNP
start: 73403488
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403489
feature_type: variation
id: rs2063046424
seq_region_name: 17
source: dbSNP
start: 73403489
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403494
feature_type: variation
id: rs2063046454
seq_region_name: 17
source: dbSNP
start: 73403494
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403496
feature_type: variation
id: rs1259457830
seq_region_name: 17
source: dbSNP
start: 73403495
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403496
feature_type: variation
id: rs549536321
seq_region_name: 17
source: dbSNP
start: 73403496
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403500
feature_type: variation
id: rs1488025368
seq_region_name: 17
source: dbSNP
start: 73403500
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403504
feature_type: variation
id: rs1286794331
seq_region_name: 17
source: dbSNP
start: 73403504
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403508
feature_type: variation
id: rs2063046526
seq_region_name: 17
source: dbSNP
start: 73403508
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403518
feature_type: variation
id: rs2063046557
seq_region_name: 17
source: dbSNP
start: 73403518
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403520
feature_type: variation
id: rs554668556
seq_region_name: 17
source: dbSNP
start: 73403520
strand: 1
-
alleles:
- TCCTC
- TCCTCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403525
feature_type: variation
id: rs1659654254
seq_region_name: 17
source: dbSNP
start: 73403521
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403530
feature_type: variation
id: rs2063046613
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-
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403721
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403728
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063047894
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73403739
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403739
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063047997
seq_region_name: 17
source: dbSNP
start: 73403740
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1012987926
seq_region_name: 17
source: dbSNP
start: 73403741
strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs1336800501
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73403752
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1024832856
seq_region_name: 17
source: dbSNP
start: 73403755
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063048135
seq_region_name: 17
source: dbSNP
start: 73403757
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs879190925
seq_region_name: 17
source: dbSNP
start: 73403760
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73403761
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063048203
seq_region_name: 17
source: dbSNP
start: 73403764
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs907342782
seq_region_name: 17
source: dbSNP
start: 73403766
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145535303
seq_region_name: 17
source: dbSNP
start: 73403767
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063048271
seq_region_name: 17
source: dbSNP
start: 73403770
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249874617
seq_region_name: 17
source: dbSNP
start: 73403774
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1465043455
seq_region_name: 17
source: dbSNP
start: 73403778
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1211779645
seq_region_name: 17
source: dbSNP
start: 73403779
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73403785
feature_type: variation
id: rs563885735
seq_region_name: 17
source: dbSNP
start: 73403783
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063048426
seq_region_name: 17
source: dbSNP
start: 73403784
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403788
feature_type: variation
id: rs2063048452
seq_region_name: 17
source: dbSNP
start: 73403788
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565157079
seq_region_name: 17
source: dbSNP
start: 73403790
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063048506
seq_region_name: 17
source: dbSNP
start: 73403792
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403795
feature_type: variation
id: rs1031847068
seq_region_name: 17
source: dbSNP
start: 73403795
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs918091389
seq_region_name: 17
source: dbSNP
start: 73403798
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs532489396
seq_region_name: 17
source: dbSNP
start: 73403800
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403804
feature_type: variation
id: rs1246172880
seq_region_name: 17
source: dbSNP
start: 73403804
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403808
feature_type: variation
id: rs2063048605
seq_region_name: 17
source: dbSNP
start: 73403808
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403809
feature_type: variation
id: rs1199913914
seq_region_name: 17
source: dbSNP
start: 73403809
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403813
feature_type: variation
id: rs1469952593
seq_region_name: 17
source: dbSNP
start: 73403813
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73403819
feature_type: variation
id: rs2063048673
seq_region_name: 17
source: dbSNP
start: 73403819
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73404001
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404008
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404009
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404011
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404013
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404016
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404025
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063050765
seq_region_name: 17
source: dbSNP
start: 73404029
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063050789
seq_region_name: 17
source: dbSNP
start: 73404033
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1378549755
seq_region_name: 17
source: dbSNP
start: 73404034
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404035
strand: 1
-
alleles:
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- TTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1158320722
seq_region_name: 17
source: dbSNP
start: 73404036
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs569767497
seq_region_name: 17
source: dbSNP
start: 73404043
strand: 1
-
alleles:
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- TAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404050
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063050979
seq_region_name: 17
source: dbSNP
start: 73404044
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404053
feature_type: variation
id: rs1599530639
seq_region_name: 17
source: dbSNP
start: 73404053
strand: 1
-
alleles:
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- A
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404233
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404234
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404234
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404235
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404243
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404247
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404256
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404259
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404260
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404267
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404272
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404275
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404279
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404280
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404281
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404282
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145536731
seq_region_name: 17
source: dbSNP
start: 73404283
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404287
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1253397408
seq_region_name: 17
source: dbSNP
start: 73404289
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73404294
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404290
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404292
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404297
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73404298
feature_type: variation
id: rs554756381
seq_region_name: 17
source: dbSNP
start: 73404298
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404299
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404300
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404300
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404478
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404481
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404495
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404498
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404500
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063054789
seq_region_name: 17
source: dbSNP
start: 73404501
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404502
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404504
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404509
strand: 1
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alleles:
- AAA
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404513
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seq_region_name: 17
source: dbSNP
start: 73404511
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404513
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404520
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73404521
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404521
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404523
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seq_region_name: 17
source: dbSNP
start: 73404523
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063055002
seq_region_name: 17
source: dbSNP
start: 73404525
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404529
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404529
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404535
feature_type: variation
id: rs2063055066
seq_region_name: 17
source: dbSNP
start: 73404535
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs989840974
seq_region_name: 17
source: dbSNP
start: 73404536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063055126
seq_region_name: 17
source: dbSNP
start: 73404542
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063055153
seq_region_name: 17
source: dbSNP
start: 73404543
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404546
feature_type: variation
id: rs2063055180
seq_region_name: 17
source: dbSNP
start: 73404546
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404549
feature_type: variation
id: rs2063055201
seq_region_name: 17
source: dbSNP
start: 73404549
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404554
feature_type: variation
id: rs1182178049
seq_region_name: 17
source: dbSNP
start: 73404554
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73404556
feature_type: variation
id: rs758328720
seq_region_name: 17
source: dbSNP
start: 73404556
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404559
feature_type: variation
id: rs542111881
seq_region_name: 17
source: dbSNP
start: 73404559
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404560
feature_type: variation
id: rs1329302718
seq_region_name: 17
source: dbSNP
start: 73404560
strand: 1
-
alleles:
- GGAGCTTGCACATGGA
- GGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404580
feature_type: variation
id: rs1210072264
seq_region_name: 17
source: dbSNP
start: 73404565
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404567
feature_type: variation
id: rs1568385087
seq_region_name: 17
source: dbSNP
start: 73404567
strand: 1
-
alleles:
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- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404569
feature_type: variation
id: rs964443616
seq_region_name: 17
source: dbSNP
start: 73404569
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404570
feature_type: variation
id: rs2063055399
seq_region_name: 17
source: dbSNP
start: 73404570
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404573
feature_type: variation
id: rs2063055426
seq_region_name: 17
source: dbSNP
start: 73404573
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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start: 73404705
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404718
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404721
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404727
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404729
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404730
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404736
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404742
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404744
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73404748
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73404750
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73404753
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145538070
seq_region_name: 17
source: dbSNP
start: 73404755
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404755
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404761
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404762
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404763
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404766
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404769
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063057239
seq_region_name: 17
source: dbSNP
start: 73404770
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs74393201
seq_region_name: 17
source: dbSNP
start: 73404773
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73404779
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73404782
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs981412688
seq_region_name: 17
source: dbSNP
start: 73404783
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404785
feature_type: variation
id: rs1163898817
seq_region_name: 17
source: dbSNP
start: 73404785
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404786
feature_type: variation
id: rs1461902182
seq_region_name: 17
source: dbSNP
start: 73404786
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404787
feature_type: variation
id: rs772954976
seq_region_name: 17
source: dbSNP
start: 73404787
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404789
feature_type: variation
id: rs139941811
seq_region_name: 17
source: dbSNP
start: 73404789
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73404791
feature_type: variation
id: rs1599531308
seq_region_name: 17
source: dbSNP
start: 73404791
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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start: 73405002
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405008
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405011
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405019
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405028
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405030
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405031
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405034
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405048
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405051
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405055
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405056
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405058
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405062
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405063
strand: 1
-
alleles:
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- TC
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405067
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1235162781
seq_region_name: 17
source: dbSNP
start: 73405069
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73405070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405072
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1015316472
seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405218
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405219
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405220
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405222
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405223
strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405224
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405225
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405226
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405227
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405230
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405232
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405235
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405236
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405238
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405239
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73405240
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seq_region_name: 17
source: dbSNP
start: 73405240
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405242
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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strand: 1
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405402
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405406
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405407
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405411
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405412
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405414
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1310503993
seq_region_name: 17
source: dbSNP
start: 73405418
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405422
feature_type: variation
id: rs1336515851
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs1011163585
seq_region_name: 17
source: dbSNP
start: 73405423
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405426
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1451444329
seq_region_name: 17
source: dbSNP
start: 73405428
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1362997411
seq_region_name: 17
source: dbSNP
start: 73405430
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs903086442
seq_region_name: 17
source: dbSNP
start: 73405432
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1473493980
seq_region_name: 17
source: dbSNP
start: 73405433
strand: 1
-
alleles:
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- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs561349181
seq_region_name: 17
source: dbSNP
start: 73405435
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs528817579
seq_region_name: 17
source: dbSNP
start: 73405436
strand: 1
-
alleles:
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- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599532131
seq_region_name: 17
source: dbSNP
start: 73405438
strand: 1
-
alleles:
- "-"
- A
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064298
seq_region_name: 17
source: dbSNP
start: 73405439
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003133593
seq_region_name: 17
source: dbSNP
start: 73405439
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568385501
seq_region_name: 17
source: dbSNP
start: 73405439
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064339
seq_region_name: 17
source: dbSNP
start: 73405439
strand: 1
-
alleles:
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- CAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064372
seq_region_name: 17
source: dbSNP
start: 73405439
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1333271337
seq_region_name: 17
source: dbSNP
start: 73405440
strand: 1
-
alleles:
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- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1230810012
seq_region_name: 17
source: dbSNP
start: 73405440
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293191900
seq_region_name: 17
source: dbSNP
start: 73405445
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405447
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064555
seq_region_name: 17
source: dbSNP
start: 73405448
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1036693799
seq_region_name: 17
source: dbSNP
start: 73405449
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1335844904
seq_region_name: 17
source: dbSNP
start: 73405450
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064628
seq_region_name: 17
source: dbSNP
start: 73405450
strand: 1
-
alleles:
- "-"
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064647
seq_region_name: 17
source: dbSNP
start: 73405451
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs112121847
seq_region_name: 17
source: dbSNP
start: 73405451
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1380112150
seq_region_name: 17
source: dbSNP
start: 73405452
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs866771410
seq_region_name: 17
source: dbSNP
start: 73405452
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1555762576
seq_region_name: 17
source: dbSNP
start: 73405452
strand: 1
-
alleles:
- AAACAAACAAA
- AAACAAA
- AAACAAACAAACAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1197587400
seq_region_name: 17
source: dbSNP
start: 73405452
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063064812
seq_region_name: 17
source: dbSNP
start: 73405453
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405453
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1415643042
seq_region_name: 17
source: dbSNP
start: 73405453
strand: 1
-
alleles:
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- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405453
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405454
strand: 1
-
alleles:
- ACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405454
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405455
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405455
strand: 1
-
alleles:
- CAAAC
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405455
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405456
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405458
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs958768511
seq_region_name: 17
source: dbSNP
start: 73405459
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063065153
seq_region_name: 17
source: dbSNP
start: 73405459
strand: 1
-
alleles:
- AAAAAA
- AA
- AAAAA
- AAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063065175
seq_region_name: 17
source: dbSNP
start: 73405460
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405463
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1467394133
seq_region_name: 17
source: dbSNP
start: 73405463
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1234425706
seq_region_name: 17
source: dbSNP
start: 73405465
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1273186137
seq_region_name: 17
source: dbSNP
start: 73405465
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs865906376
seq_region_name: 17
source: dbSNP
start: 73405466
strand: 1
-
alleles:
- CC
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1356454817
seq_region_name: 17
source: dbSNP
start: 73405466
strand: 1
-
alleles:
- CCAT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1285380605
seq_region_name: 17
source: dbSNP
start: 73405466
strand: 1
-
alleles:
- CCATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1224824905
seq_region_name: 17
source: dbSNP
start: 73405466
strand: 1
-
alleles:
- CCATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405473
feature_type: variation
id: rs2063065415
seq_region_name: 17
source: dbSNP
start: 73405466
strand: 1
-
alleles:
- CCATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063065442
seq_region_name: 17
source: dbSNP
start: 73405466
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1437057292
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063065482
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405468
feature_type: variation
id: rs2063065500
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
- CATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405470
feature_type: variation
id: rs1568385558
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
- CATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405471
feature_type: variation
id: rs2063065550
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
- CATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405472
feature_type: variation
id: rs1568385561
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
- CATATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405474
feature_type: variation
id: rs1568385565
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
- CATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405477
feature_type: variation
id: rs1568385569
seq_region_name: 17
source: dbSNP
start: 73405467
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405468
feature_type: variation
id: rs1302369961
seq_region_name: 17
source: dbSNP
start: 73405468
strand: 1
-
alleles:
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- ATATATATATATATA
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- ATATATATATATATATATA
- ATATATATATATATATATATA
- ATATATATATATATATATATATA
- ATATATATATATATATATATATATA
- ATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
- ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405518
feature_type: variation
id: rs1166184210
seq_region_name: 17
source: dbSNP
start: 73405468
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405469
feature_type: variation
id: rs1276219604
seq_region_name: 17
source: dbSNP
start: 73405469
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405469
feature_type: variation
id: rs2063065866
seq_region_name: 17
source: dbSNP
start: 73405469
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405470
feature_type: variation
id: rs1351598111
seq_region_name: 17
source: dbSNP
start: 73405470
strand: 1
-
alleles:
- A
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405470
feature_type: variation
id: rs2063065921
seq_region_name: 17
source: dbSNP
start: 73405470
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405470
feature_type: variation
id: rs2145540948
seq_region_name: 17
source: dbSNP
start: 73405470
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405471
feature_type: variation
id: rs1326736398
seq_region_name: 17
source: dbSNP
start: 73405471
strand: 1
-
alleles:
- TATATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405483
feature_type: variation
id: rs2145540967
seq_region_name: 17
source: dbSNP
start: 73405471
strand: 1
-
alleles:
- TATATATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405485
feature_type: variation
id: rs2145540974
seq_region_name: 17
source: dbSNP
start: 73405471
strand: 1
-
alleles:
- TATATATATATATATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405493
feature_type: variation
id: rs2063065973
seq_region_name: 17
source: dbSNP
start: 73405471
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405472
feature_type: variation
id: rs1409527073
seq_region_name: 17
source: dbSNP
start: 73405472
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405472
feature_type: variation
id: rs2063066015
seq_region_name: 17
source: dbSNP
start: 73405472
strand: 1
-
alleles:
- ATATATATATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405484
feature_type: variation
id: rs2145541007
seq_region_name: 17
source: dbSNP
start: 73405472
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405473
feature_type: variation
id: rs1599532310
seq_region_name: 17
source: dbSNP
start: 73405473
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405473
feature_type: variation
id: rs2145541025
seq_region_name: 17
source: dbSNP
start: 73405473
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405474
feature_type: variation
id: rs1371231291
seq_region_name: 17
source: dbSNP
start: 73405474
strand: 1
-
alleles:
- ATATATATATATATATATATATATATATATATATATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405512
feature_type: variation
id: rs2063066087
seq_region_name: 17
source: dbSNP
start: 73405474
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405475
feature_type: variation
id: rs1599532315
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405481
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405481
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405482
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405483
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405485
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405485
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1362562663
seq_region_name: 17
source: dbSNP
start: 73405485
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405487
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405487
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73405487
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405488
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405488
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405490
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405491
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405491
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405491
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405493
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405493
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405493
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405493
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405493
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73405493
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405495
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73405495
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405497
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405497
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405497
strand: 1
-
alleles:
- TATATATATATAT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405509
feature_type: variation
id: rs1568385696
seq_region_name: 17
source: dbSNP
start: 73405497
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405513
feature_type: variation
id: rs1568385698
seq_region_name: 17
source: dbSNP
start: 73405497
strand: 1
-
alleles:
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- ACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405498
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405498
feature_type: variation
id: rs2063067511
seq_region_name: 17
source: dbSNP
start: 73405498
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405499
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568385701
seq_region_name: 17
source: dbSNP
start: 73405499
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568385707
seq_region_name: 17
source: dbSNP
start: 73405499
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405513
feature_type: variation
id: rs1568385710
seq_region_name: 17
source: dbSNP
start: 73405499
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405517
feature_type: variation
id: rs2063067623
seq_region_name: 17
source: dbSNP
start: 73405499
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405501
feature_type: variation
id: rs528598886
seq_region_name: 17
source: dbSNP
start: 73405501
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405501
feature_type: variation
id: rs1423495931
seq_region_name: 17
source: dbSNP
start: 73405501
strand: 1
-
alleles:
- TATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405505
feature_type: variation
id: rs2063067698
seq_region_name: 17
source: dbSNP
start: 73405501
strand: 1
-
alleles:
- TATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405507
feature_type: variation
id: rs2063067723
seq_region_name: 17
source: dbSNP
start: 73405501
strand: 1
-
alleles:
- TATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405509
feature_type: variation
id: rs1568385716
seq_region_name: 17
source: dbSNP
start: 73405501
strand: 1
-
alleles:
- TATATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405513
feature_type: variation
id: rs1568385719
seq_region_name: 17
source: dbSNP
start: 73405501
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405503
feature_type: variation
id: rs1414192227
seq_region_name: 17
source: dbSNP
start: 73405503
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405503
feature_type: variation
id: rs1568385722
seq_region_name: 17
source: dbSNP
start: 73405503
strand: 1
-
alleles:
- TATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405509
feature_type: variation
id: rs1568385724
seq_region_name: 17
source: dbSNP
start: 73405503
strand: 1
-
alleles:
- TATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405513
feature_type: variation
id: rs1568385726
seq_region_name: 17
source: dbSNP
start: 73405503
strand: 1
-
alleles:
- TATATATATATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405517
feature_type: variation
id: rs2063067882
seq_region_name: 17
source: dbSNP
start: 73405503
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405504
feature_type: variation
id: rs1441320400
seq_region_name: 17
source: dbSNP
start: 73405504
strand: 1
-
alleles:
- A
- AAA
- ACATACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405504
feature_type: variation
id: rs2063067918
seq_region_name: 17
source: dbSNP
start: 73405504
strand: 1
-
alleles:
- ATA
- ATACATACATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405506
feature_type: variation
id: rs2063067943
seq_region_name: 17
source: dbSNP
start: 73405504
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405505
feature_type: variation
id: rs56299628
seq_region_name: 17
source: dbSNP
start: 73405505
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405505
feature_type: variation
id: rs1351191084
seq_region_name: 17
source: dbSNP
start: 73405505
strand: 1
-
alleles:
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- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405505
feature_type: variation
id: rs1369464278
seq_region_name: 17
source: dbSNP
start: 73405505
strand: 1
-
alleles:
- TAT
- TATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405507
feature_type: variation
id: rs1555762621
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405507
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405508
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405508
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs990951587
seq_region_name: 17
source: dbSNP
start: 73405509
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405509
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405509
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405509
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405510
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405511
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405512
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73405513
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405513
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405513
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405514
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405514
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405515
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405515
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063069195
seq_region_name: 17
source: dbSNP
start: 73405515
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405515
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405516
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405516
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405516
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405517
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405517
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063069369
seq_region_name: 17
source: dbSNP
start: 73405518
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405518
feature_type: variation
id: rs750250733
seq_region_name: 17
source: dbSNP
start: 73405518
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405520
feature_type: variation
id: rs112566588
seq_region_name: 17
source: dbSNP
start: 73405518
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405518
feature_type: variation
id: rs2063069541
seq_region_name: 17
source: dbSNP
start: 73405519
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1403021241
seq_region_name: 17
source: dbSNP
start: 73405519
strand: 1
-
alleles:
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- TATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063069601
seq_region_name: 17
source: dbSNP
start: 73405520
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405520
feature_type: variation
id: rs2063069635
seq_region_name: 17
source: dbSNP
start: 73405520
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405521
feature_type: variation
id: rs1330725418
seq_region_name: 17
source: dbSNP
start: 73405521
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405525
feature_type: variation
id: rs1445257174
seq_region_name: 17
source: dbSNP
start: 73405521
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405527
feature_type: variation
id: rs2145542254
seq_region_name: 17
source: dbSNP
start: 73405521
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405534
feature_type: variation
id: rs2063069682
seq_region_name: 17
source: dbSNP
start: 73405521
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405522
feature_type: variation
id: rs2063069703
seq_region_name: 17
source: dbSNP
start: 73405522
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405523
feature_type: variation
id: rs2063069715
seq_region_name: 17
source: dbSNP
start: 73405523
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405525
feature_type: variation
id: rs1371877145
seq_region_name: 17
source: dbSNP
start: 73405523
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405524
feature_type: variation
id: rs1438860776
seq_region_name: 17
source: dbSNP
start: 73405524
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405525
feature_type: variation
id: rs2063069793
seq_region_name: 17
source: dbSNP
start: 73405525
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405527
feature_type: variation
id: rs1273365883
seq_region_name: 17
source: dbSNP
start: 73405527
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405529
feature_type: variation
id: rs2063069836
seq_region_name: 17
source: dbSNP
start: 73405529
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405530
feature_type: variation
id: rs2145542310
seq_region_name: 17
source: dbSNP
start: 73405530
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405534
feature_type: variation
id: rs2145542316
seq_region_name: 17
source: dbSNP
start: 73405530
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405531
feature_type: variation
id: rs2145542322
seq_region_name: 17
source: dbSNP
start: 73405531
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405534
feature_type: variation
id: rs1344585035
seq_region_name: 17
source: dbSNP
start: 73405534
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405536
feature_type: variation
id: rs2145542336
seq_region_name: 17
source: dbSNP
start: 73405536
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405539
feature_type: variation
id: rs2063069887
seq_region_name: 17
source: dbSNP
start: 73405539
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405541
feature_type: variation
id: rs2145542355
seq_region_name: 17
source: dbSNP
start: 73405541
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405711
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405715
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405715
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405716
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73405718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73405719
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405720
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405723
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405724
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405724
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405725
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405728
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405730
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs940979979
seq_region_name: 17
source: dbSNP
start: 73405738
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405738
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405739
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405742
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405743
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405743
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405746
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405749
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73405750
feature_type: variation
id: rs569241956
seq_region_name: 17
source: dbSNP
start: 73405750
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405751
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73405754
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405754
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405756
feature_type: variation
id: rs2063072075
seq_region_name: 17
source: dbSNP
start: 73405756
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405758
feature_type: variation
id: rs1217927279
seq_region_name: 17
source: dbSNP
start: 73405758
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405759
feature_type: variation
id: rs1293756462
seq_region_name: 17
source: dbSNP
start: 73405759
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405880
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405887
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73405894
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73405897
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73405899
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405900
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405903
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405906
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405907
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73405908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1367956125
seq_region_name: 17
source: dbSNP
start: 73405913
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1406089801
seq_region_name: 17
source: dbSNP
start: 73405914
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1010089560
seq_region_name: 17
source: dbSNP
start: 73405915
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73405917
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73405921
feature_type: variation
id: rs1429309125
seq_region_name: 17
source: dbSNP
start: 73405921
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1391197835
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs998340148
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063075490
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73406018
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73406024
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73406033
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs940860032
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73406037
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs973625583
seq_region_name: 17
source: dbSNP
start: 73406038
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406043
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406044
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406046
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406056
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406056
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73406059
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406060
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
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start: 73406060
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406067
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73406070
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs920864099
seq_region_name: 17
source: dbSNP
start: 73406071
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406076
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406078
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406079
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1044066842
seq_region_name: 17
source: dbSNP
start: 73406080
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063076181
seq_region_name: 17
source: dbSNP
start: 73406081
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406087
feature_type: variation
id: rs1440491325
seq_region_name: 17
source: dbSNP
start: 73406087
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406092
feature_type: variation
id: rs1347657399
seq_region_name: 17
source: dbSNP
start: 73406092
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1277608757
seq_region_name: 17
source: dbSNP
start: 73406095
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs994741248
seq_region_name: 17
source: dbSNP
start: 73406096
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063076294
seq_region_name: 17
source: dbSNP
start: 73406098
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406100
feature_type: variation
id: rs1023535708
seq_region_name: 17
source: dbSNP
start: 73406100
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406103
feature_type: variation
id: rs1347104085
seq_region_name: 17
source: dbSNP
start: 73406103
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406105
feature_type: variation
id: rs1286348684
seq_region_name: 17
source: dbSNP
start: 73406105
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406106
feature_type: variation
id: rs969724294
seq_region_name: 17
source: dbSNP
start: 73406106
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406108
feature_type: variation
id: rs938430890
seq_region_name: 17
source: dbSNP
start: 73406108
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1310103583
seq_region_name: 17
source: dbSNP
start: 73406114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406119
feature_type: variation
id: rs1568386077
seq_region_name: 17
source: dbSNP
start: 73406115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406117
feature_type: variation
id: rs2063076449
seq_region_name: 17
source: dbSNP
start: 73406117
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406121
feature_type: variation
id: rs2063076475
seq_region_name: 17
source: dbSNP
start: 73406121
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406123
feature_type: variation
id: rs549499705
seq_region_name: 17
source: dbSNP
start: 73406123
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406125
feature_type: variation
id: rs927791809
seq_region_name: 17
source: dbSNP
start: 73406125
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406127
feature_type: variation
id: rs1416497318
seq_region_name: 17
source: dbSNP
start: 73406127
strand: 1
-
alleles:
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- AAA
- AAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406134
feature_type: variation
id: rs1159064808
seq_region_name: 17
source: dbSNP
start: 73406129
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406138
feature_type: variation
id: rs1472009687
seq_region_name: 17
source: dbSNP
start: 73406135
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406138
feature_type: variation
id: rs1178611290
seq_region_name: 17
source: dbSNP
start: 73406138
strand: 1
-
alleles:
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- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406141
feature_type: variation
id: rs760272951
seq_region_name: 17
source: dbSNP
start: 73406138
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406139
feature_type: variation
id: rs557952573
seq_region_name: 17
source: dbSNP
start: 73406139
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406141
feature_type: variation
id: rs2145544032
seq_region_name: 17
source: dbSNP
start: 73406141
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406144
feature_type: variation
id: rs2063076686
seq_region_name: 17
source: dbSNP
start: 73406144
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406149
feature_type: variation
id: rs956810317
seq_region_name: 17
source: dbSNP
start: 73406149
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406152
feature_type: variation
id: rs988217845
seq_region_name: 17
source: dbSNP
start: 73406152
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406154
feature_type: variation
id: rs775907830
seq_region_name: 17
source: dbSNP
start: 73406154
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406155
feature_type: variation
id: rs1210607971
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strand: 1
-
alleles:
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feature_type: variation
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-
alleles:
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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feature_type: variation
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strand: 1
-
alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406227
strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406234
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1386889989
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73406253
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs200985329
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73406262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406264
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406268
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73406274
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406275
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406278
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73406284
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406285
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73406286
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406287
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406288
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599533613
seq_region_name: 17
source: dbSNP
start: 73406292
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406293
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406296
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1303043815
seq_region_name: 17
source: dbSNP
start: 73406300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1329006059
seq_region_name: 17
source: dbSNP
start: 73406304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406305
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1426040484
seq_region_name: 17
source: dbSNP
start: 73406311
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1051231955
seq_region_name: 17
source: dbSNP
start: 73406313
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1368027253
seq_region_name: 17
source: dbSNP
start: 73406314
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063078806
seq_region_name: 17
source: dbSNP
start: 73406316
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063078829
seq_region_name: 17
source: dbSNP
start: 73406317
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs190041190
seq_region_name: 17
source: dbSNP
start: 73406321
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063078872
seq_region_name: 17
source: dbSNP
start: 73406325
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73406328
feature_type: variation
id: rs2063078903
seq_region_name: 17
source: dbSNP
start: 73406328
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406329
feature_type: variation
id: rs1004624454
seq_region_name: 17
source: dbSNP
start: 73406329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406332
feature_type: variation
id: rs1036138797
seq_region_name: 17
source: dbSNP
start: 73406332
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1165048079
seq_region_name: 17
source: dbSNP
start: 73406336
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406339
feature_type: variation
id: rs1426120718
seq_region_name: 17
source: dbSNP
start: 73406339
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs898936269
seq_region_name: 17
source: dbSNP
start: 73406343
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs994478884
seq_region_name: 17
source: dbSNP
start: 73406346
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73406351
feature_type: variation
id: rs2063079044
seq_region_name: 17
source: dbSNP
start: 73406351
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406354
feature_type: variation
id: rs2145544575
seq_region_name: 17
source: dbSNP
start: 73406354
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406356
feature_type: variation
id: rs2063079064
seq_region_name: 17
source: dbSNP
start: 73406356
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406358
feature_type: variation
id: rs2063079092
seq_region_name: 17
source: dbSNP
start: 73406357
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406360
feature_type: variation
id: rs2063079123
seq_region_name: 17
source: dbSNP
start: 73406360
strand: 1
-
alleles:
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- GGCAAGAGAGAGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406362
feature_type: variation
id: rs2063079142
seq_region_name: 17
source: dbSNP
start: 73406362
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406363
feature_type: variation
id: rs2063079164
seq_region_name: 17
source: dbSNP
start: 73406363
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406366
feature_type: variation
id: rs1449813122
seq_region_name: 17
source: dbSNP
start: 73406366
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406368
feature_type: variation
id: rs1263846109
seq_region_name: 17
source: dbSNP
start: 73406368
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406371
feature_type: variation
id: rs1256219702
seq_region_name: 17
source: dbSNP
start: 73406371
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406372
feature_type: variation
id: rs1457422853
seq_region_name: 17
source: dbSNP
start: 73406372
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406375
feature_type: variation
id: rs2063079297
seq_region_name: 17
source: dbSNP
start: 73406375
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73406541
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73406566
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406572
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73406574
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406576
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73406577
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73406580
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063081463
seq_region_name: 17
source: dbSNP
start: 73406581
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063081497
seq_region_name: 17
source: dbSNP
start: 73406584
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs749799836
seq_region_name: 17
source: dbSNP
start: 73406585
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406590
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406599
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs968063323
seq_region_name: 17
source: dbSNP
start: 73406603
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73406604
feature_type: variation
id: rs975507437
seq_region_name: 17
source: dbSNP
start: 73406604
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406605
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id: rs12944702
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406800
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73406804
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406811
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406813
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73406823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063083160
seq_region_name: 17
source: dbSNP
start: 73406828
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406830
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1264610445
seq_region_name: 17
source: dbSNP
start: 73406832
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73406835
strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs1022080278
seq_region_name: 17
source: dbSNP
start: 73406838
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568386367
seq_region_name: 17
source: dbSNP
start: 73406839
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1262248744
seq_region_name: 17
source: dbSNP
start: 73406842
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs903729050
seq_region_name: 17
source: dbSNP
start: 73406845
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1229431940
seq_region_name: 17
source: dbSNP
start: 73406855
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1329448231
seq_region_name: 17
source: dbSNP
start: 73406860
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063083416
seq_region_name: 17
source: dbSNP
start: 73406861
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs772335174
seq_region_name: 17
source: dbSNP
start: 73406864
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063083495
seq_region_name: 17
source: dbSNP
start: 73406867
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406869
feature_type: variation
id: rs978945735
seq_region_name: 17
source: dbSNP
start: 73406869
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406870
feature_type: variation
id: rs2063083549
seq_region_name: 17
source: dbSNP
start: 73406870
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406872
feature_type: variation
id: rs1405605463
seq_region_name: 17
source: dbSNP
start: 73406872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406880
feature_type: variation
id: rs1367763942
seq_region_name: 17
source: dbSNP
start: 73406873
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406876
feature_type: variation
id: rs1599534159
seq_region_name: 17
source: dbSNP
start: 73406876
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406879
feature_type: variation
id: rs925786743
seq_region_name: 17
source: dbSNP
start: 73406879
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406883
feature_type: variation
id: rs1895535616
seq_region_name: 17
source: dbSNP
start: 73406883
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406892
feature_type: variation
id: rs2063083673
seq_region_name: 17
source: dbSNP
start: 73406892
strand: 1
-
alleles:
- AAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406896
feature_type: variation
id: rs2063083702
seq_region_name: 17
source: dbSNP
start: 73406894
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73406898
feature_type: variation
id: rs2063083725
seq_region_name: 17
source: dbSNP
start: 73406898
strand: 1
-
alleles:
- C
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73407014
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407018
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73407021
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407022
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407023
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407024
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407029
strand: 1
-
alleles:
- AAA
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407034
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1331356573
seq_region_name: 17
source: dbSNP
start: 73407037
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407039
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs905330152
seq_region_name: 17
source: dbSNP
start: 73407042
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407042
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407044
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407045
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407047
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407051
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407062
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407066
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407066
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407068
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407068
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs866616332
seq_region_name: 17
source: dbSNP
start: 73407069
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063085077
seq_region_name: 17
source: dbSNP
start: 73407070
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1430702233
seq_region_name: 17
source: dbSNP
start: 73407075
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407078
feature_type: variation
id: rs1179606744
seq_region_name: 17
source: dbSNP
start: 73407078
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407082
feature_type: variation
id: rs2063085150
seq_region_name: 17
source: dbSNP
start: 73407082
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599534333
seq_region_name: 17
source: dbSNP
start: 73407083
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407084
feature_type: variation
id: rs2063085204
seq_region_name: 17
source: dbSNP
start: 73407084
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407087
feature_type: variation
id: rs1599534336
seq_region_name: 17
source: dbSNP
start: 73407087
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407088
feature_type: variation
id: rs2063085259
seq_region_name: 17
source: dbSNP
start: 73407088
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407092
feature_type: variation
id: rs2063085292
seq_region_name: 17
source: dbSNP
start: 73407092
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407095
feature_type: variation
id: rs1599534342
seq_region_name: 17
source: dbSNP
start: 73407095
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407096
feature_type: variation
id: rs1472031777
seq_region_name: 17
source: dbSNP
start: 73407096
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407097
feature_type: variation
id: rs2063085362
seq_region_name: 17
source: dbSNP
start: 73407097
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407098
feature_type: variation
id: rs1233074545
seq_region_name: 17
source: dbSNP
start: 73407098
strand: 1
-
alleles:
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- TAGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407108
feature_type: variation
id: rs1314236094
seq_region_name: 17
source: dbSNP
start: 73407101
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407102
feature_type: variation
id: rs2063085443
seq_region_name: 17
source: dbSNP
start: 73407102
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407103
feature_type: variation
id: rs1599534356
seq_region_name: 17
source: dbSNP
start: 73407103
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407104
feature_type: variation
id: rs1178904219
seq_region_name: 17
source: dbSNP
start: 73407104
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407110
feature_type: variation
id: rs1440471161
seq_region_name: 17
source: dbSNP
start: 73407110
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407114
feature_type: variation
id: rs1277849129
seq_region_name: 17
source: dbSNP
start: 73407114
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407119
feature_type: variation
id: rs2063085572
seq_region_name: 17
source: dbSNP
start: 73407119
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407123
feature_type: variation
id: rs2063085601
seq_region_name: 17
source: dbSNP
start: 73407123
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407129
feature_type: variation
id: rs2063085614
seq_region_name: 17
source: dbSNP
start: 73407129
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407130
feature_type: variation
id: rs1599534378
seq_region_name: 17
source: dbSNP
start: 73407130
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407132
feature_type: variation
id: rs367965865
seq_region_name: 17
source: dbSNP
start: 73407132
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407133
feature_type: variation
id: rs8082141
seq_region_name: 17
source: dbSNP
start: 73407133
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407134
feature_type: variation
id: rs1568386469
seq_region_name: 17
source: dbSNP
start: 73407134
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407135
feature_type: variation
id: rs2063085769
seq_region_name: 17
source: dbSNP
start: 73407134
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407135
feature_type: variation
id: rs2063085796
seq_region_name: 17
source: dbSNP
start: 73407135
strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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alleles:
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-
alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407277
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407285
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407287
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407290
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407290
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407296
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407297
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407300
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407307
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407316
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407318
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407320
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407322
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407323
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs569241399
seq_region_name: 17
source: dbSNP
start: 73407324
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs777513565
seq_region_name: 17
source: dbSNP
start: 73407326
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs761578689
seq_region_name: 17
source: dbSNP
start: 73407328
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063087340
seq_region_name: 17
source: dbSNP
start: 73407330
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73407331
feature_type: variation
id: rs891168013
seq_region_name: 17
source: dbSNP
start: 73407331
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407334
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407339
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407342
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407344
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407346
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1008351384
seq_region_name: 17
source: dbSNP
start: 73407347
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063087567
seq_region_name: 17
source: dbSNP
start: 73407348
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73407353
feature_type: variation
id: rs2063087590
seq_region_name: 17
source: dbSNP
start: 73407353
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407356
feature_type: variation
id: rs2063087619
seq_region_name: 17
source: dbSNP
start: 73407355
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407358
feature_type: variation
id: rs539439656
seq_region_name: 17
source: dbSNP
start: 73407358
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1164026384
seq_region_name: 17
source: dbSNP
start: 73407360
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73407361
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407361
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73407369
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407369
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407373
feature_type: variation
id: rs185755430
seq_region_name: 17
source: dbSNP
start: 73407373
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73407376
feature_type: variation
id: rs753993374
seq_region_name: 17
source: dbSNP
start: 73407376
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73407382
feature_type: variation
id: rs961399783
seq_region_name: 17
source: dbSNP
start: 73407382
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407384
feature_type: variation
id: rs2063087813
seq_region_name: 17
source: dbSNP
start: 73407384
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407388
feature_type: variation
id: rs117652688
seq_region_name: 17
source: dbSNP
start: 73407388
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407392
feature_type: variation
id: rs2063087889
seq_region_name: 17
source: dbSNP
start: 73407392
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407393
feature_type: variation
id: rs2063087922
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407579
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73407581
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407583
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407586
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407587
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407587
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407588
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407594
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407597
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407605
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407607
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407614
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1021654
seq_region_name: 17
source: dbSNP
start: 73407615
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407615
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1026994721
seq_region_name: 17
source: dbSNP
start: 73407616
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs573592165
seq_region_name: 17
source: dbSNP
start: 73407617
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599534840
seq_region_name: 17
source: dbSNP
start: 73407618
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407618
feature_type: variation
id: rs1480386813
seq_region_name: 17
source: dbSNP
start: 73407618
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407620
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145547865
seq_region_name: 17
source: dbSNP
start: 73407622
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407623
feature_type: variation
id: rs540885559
seq_region_name: 17
source: dbSNP
start: 73407623
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407624
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407624
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407626
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407633
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407633
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407635
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407635
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407636
feature_type: variation
id: rs2063089831
seq_region_name: 17
source: dbSNP
start: 73407636
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407642
feature_type: variation
id: rs772376630
seq_region_name: 17
source: dbSNP
start: 73407642
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407646
feature_type: variation
id: rs2063089888
seq_region_name: 17
source: dbSNP
start: 73407646
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407647
feature_type: variation
id: rs938079261
seq_region_name: 17
source: dbSNP
start: 73407647
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407648
feature_type: variation
id: rs1056496032
seq_region_name: 17
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-
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alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407701
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407755
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407764
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407770
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407775
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407776
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407779
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407790
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063091209
seq_region_name: 17
source: dbSNP
start: 73407791
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145548376
seq_region_name: 17
source: dbSNP
start: 73407793
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73407794
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs931387281
seq_region_name: 17
source: dbSNP
start: 73407796
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407799
feature_type: variation
id: rs1042528358
seq_region_name: 17
source: dbSNP
start: 73407799
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73407806
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407807
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73407807
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1426473433
seq_region_name: 17
source: dbSNP
start: 73407815
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063091461
seq_region_name: 17
source: dbSNP
start: 73407822
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407830
feature_type: variation
id: rs1599535077
seq_region_name: 17
source: dbSNP
start: 73407830
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407831
feature_type: variation
id: rs2063091500
seq_region_name: 17
source: dbSNP
start: 73407831
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407836
feature_type: variation
id: rs35493050
seq_region_name: 17
source: dbSNP
start: 73407832
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407835
feature_type: variation
id: rs2063091576
seq_region_name: 17
source: dbSNP
start: 73407835
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407840
feature_type: variation
id: rs374937832
seq_region_name: 17
source: dbSNP
start: 73407837
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407838
feature_type: variation
id: rs1048423974
seq_region_name: 17
source: dbSNP
start: 73407838
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407841
feature_type: variation
id: rs2145548492
seq_region_name: 17
source: dbSNP
start: 73407841
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407846
feature_type: variation
id: rs2145548505
seq_region_name: 17
source: dbSNP
start: 73407846
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407852
feature_type: variation
id: rs1387695466
seq_region_name: 17
source: dbSNP
start: 73407852
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407854
feature_type: variation
id: rs2063091722
seq_region_name: 17
source: dbSNP
start: 73407854
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407858
feature_type: variation
id: rs2063091745
seq_region_name: 17
source: dbSNP
start: 73407858
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407869
feature_type: variation
id: rs1187163249
seq_region_name: 17
source: dbSNP
start: 73407869
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407874
feature_type: variation
id: rs1444784918
seq_region_name: 17
source: dbSNP
start: 73407874
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407878
feature_type: variation
id: rs1001507310
seq_region_name: 17
source: dbSNP
start: 73407878
strand: 1
-
alleles:
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- AAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407889
feature_type: variation
id: rs2145548557
seq_region_name: 17
source: dbSNP
start: 73407882
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407885
feature_type: variation
id: rs1167440859
seq_region_name: 17
source: dbSNP
start: 73407885
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407886
feature_type: variation
id: rs1050030059
seq_region_name: 17
source: dbSNP
start: 73407886
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407887
feature_type: variation
id: rs2063091817
seq_region_name: 17
source: dbSNP
start: 73407887
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407892
feature_type: variation
id: rs72853988
seq_region_name: 17
source: dbSNP
start: 73407892
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407894
feature_type: variation
id: rs2063091888
seq_region_name: 17
source: dbSNP
start: 73407894
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407896
feature_type: variation
id: rs1002178215
seq_region_name: 17
source: dbSNP
start: 73407896
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407898
feature_type: variation
id: rs1407307060
seq_region_name: 17
source: dbSNP
start: 73407898
strand: 1
-
alleles:
- ATAATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73407903
feature_type: variation
id: rs2063091969
seq_region_name: 17
source: dbSNP
start: 73407898
strand: 1
-
alleles:
- AA
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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alleles:
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73407981
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408023
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408024
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408024
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408027
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408030
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408035
strand: 1
-
alleles:
- AAAA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73408041
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408042
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408042
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408043
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408043
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408046
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408046
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408046
strand: 1
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alleles:
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1405734601
seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1367659384
seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1397907123
seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063094029
seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1170093310
seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063094097
seq_region_name: 17
source: dbSNP
start: 73408048
strand: 1
-
alleles:
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408064
feature_type: variation
id: rs951934202
seq_region_name: 17
source: dbSNP
start: 73408048
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408050
feature_type: variation
id: rs1020414287
seq_region_name: 17
source: dbSNP
start: 73408050
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408051
feature_type: variation
id: rs966433371
seq_region_name: 17
source: dbSNP
start: 73408051
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408051
feature_type: variation
id: rs1445796065
seq_region_name: 17
source: dbSNP
start: 73408051
strand: 1
-
alleles:
- TTTT
- TTTTCTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408054
feature_type: variation
id: rs2063094204
seq_region_name: 17
source: dbSNP
start: 73408051
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408051
feature_type: variation
id: rs1273643354
seq_region_name: 17
source: dbSNP
start: 73408052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408052
feature_type: variation
id: rs979185251
seq_region_name: 17
source: dbSNP
start: 73408052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- TTTTTTTGGT
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063094970
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408072
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063095055
seq_region_name: 17
source: dbSNP
start: 73408074
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408075
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73408083
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408084
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408086
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73408088
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063095228
seq_region_name: 17
source: dbSNP
start: 73408089
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs8068263
seq_region_name: 17
source: dbSNP
start: 73408090
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1175132334
seq_region_name: 17
source: dbSNP
start: 73408091
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063095274
seq_region_name: 17
source: dbSNP
start: 73408095
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568386914
seq_region_name: 17
source: dbSNP
start: 73408096
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408097
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063095356
seq_region_name: 17
source: dbSNP
start: 73408099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063095382
seq_region_name: 17
source: dbSNP
start: 73408099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408101
strand: 1
-
alleles:
- AGTACAAT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408109
feature_type: variation
id: rs2063095436
seq_region_name: 17
source: dbSNP
start: 73408102
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1032410927
seq_region_name: 17
source: dbSNP
start: 73408113
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1033611559
seq_region_name: 17
source: dbSNP
start: 73408115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063095517
seq_region_name: 17
source: dbSNP
start: 73408116
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063095537
seq_region_name: 17
source: dbSNP
start: 73408118
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs116705700
seq_region_name: 17
source: dbSNP
start: 73408127
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1280019410
seq_region_name: 17
source: dbSNP
start: 73408130
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599535448
seq_region_name: 17
source: dbSNP
start: 73408132
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs572045172
seq_region_name: 17
source: dbSNP
start: 73408134
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1233203867
seq_region_name: 17
source: dbSNP
start: 73408138
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs149030862
seq_region_name: 17
source: dbSNP
start: 73408140
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063095695
seq_region_name: 17
source: dbSNP
start: 73408149
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408152
feature_type: variation
id: rs2063095718
seq_region_name: 17
source: dbSNP
start: 73408152
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408153
feature_type: variation
id: rs912451548
seq_region_name: 17
source: dbSNP
start: 73408153
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408154
feature_type: variation
id: rs943959728
seq_region_name: 17
source: dbSNP
start: 73408154
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408155
feature_type: variation
id: rs2063095793
seq_region_name: 17
source: dbSNP
start: 73408155
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408157
feature_type: variation
id: rs972521411
seq_region_name: 17
source: dbSNP
start: 73408157
strand: 1
-
alleles:
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- TTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408163
feature_type: variation
id: rs1242450041
seq_region_name: 17
source: dbSNP
start: 73408157
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408169
feature_type: variation
id: rs2063095894
seq_region_name: 17
source: dbSNP
start: 73408169
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408172
feature_type: variation
id: rs555770403
seq_region_name: 17
source: dbSNP
start: 73408172
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408174
feature_type: variation
id: rs2145549897
seq_region_name: 17
source: dbSNP
start: 73408174
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408175
feature_type: variation
id: rs2063095951
seq_region_name: 17
source: dbSNP
start: 73408175
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408176
feature_type: variation
id: rs574206540
seq_region_name: 17
source: dbSNP
start: 73408176
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408177
feature_type: variation
id: rs183676473
seq_region_name: 17
source: dbSNP
start: 73408177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408179
feature_type: variation
id: rs2063096035
seq_region_name: 17
source: dbSNP
start: 73408179
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408182
feature_type: variation
id: rs931375613
seq_region_name: 17
source: dbSNP
start: 73408182
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408187
feature_type: variation
id: rs2063096083
seq_region_name: 17
source: dbSNP
start: 73408187
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408192
feature_type: variation
id: rs8067289
seq_region_name: 17
source: dbSNP
start: 73408192
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408195
feature_type: variation
id: rs1382783501
seq_region_name: 17
source: dbSNP
start: 73408195
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408196
feature_type: variation
id: rs2063096138
seq_region_name: 17
source: dbSNP
start: 73408196
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408197
feature_type: variation
id: rs890044718
seq_region_name: 17
source: dbSNP
start: 73408197
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408201
feature_type: variation
id: rs1452743676
seq_region_name: 17
source: dbSNP
start: 73408201
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408204
feature_type: variation
id: rs924342249
seq_region_name: 17
source: dbSNP
start: 73408204
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408209
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73408211
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063096389
seq_region_name: 17
source: dbSNP
start: 73408219
strand: 1
-
alleles:
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- TTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408219
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408225
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063096540
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1040052249
seq_region_name: 17
source: dbSNP
start: 73408229
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408231
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408232
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063096634
seq_region_name: 17
source: dbSNP
start: 73408234
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs938311145
seq_region_name: 17
source: dbSNP
start: 73408236
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063096679
seq_region_name: 17
source: dbSNP
start: 73408236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1468131618
seq_region_name: 17
source: dbSNP
start: 73408237
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1335521680
seq_region_name: 17
source: dbSNP
start: 73408238
strand: 1
-
alleles:
- "-"
- CAGAGTCTGGCTCTGT
- CAGAGTCTGGCTCTGTTGCCTAGACTGGAGTACAATGGTGTGATCTCTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408239
feature_type: variation
id: rs2063096717
seq_region_name: 17
source: dbSNP
start: 73408240
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1448538309
seq_region_name: 17
source: dbSNP
start: 73408240
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408241
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408242
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1447843987
seq_region_name: 17
source: dbSNP
start: 73408243
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063096875
seq_region_name: 17
source: dbSNP
start: 73408244
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599535587
seq_region_name: 17
source: dbSNP
start: 73408245
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1238840083
seq_region_name: 17
source: dbSNP
start: 73408248
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1275776750
seq_region_name: 17
source: dbSNP
start: 73408249
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs901537944
seq_region_name: 17
source: dbSNP
start: 73408252
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1380737417
seq_region_name: 17
source: dbSNP
start: 73408254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1347785407
seq_region_name: 17
source: dbSNP
start: 73408256
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1202273887
seq_region_name: 17
source: dbSNP
start: 73408257
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1262600426
seq_region_name: 17
source: dbSNP
start: 73408259
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408260
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063097135
seq_region_name: 17
source: dbSNP
start: 73408262
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1200592813
seq_region_name: 17
source: dbSNP
start: 73408263
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408264
feature_type: variation
id: rs2063097181
seq_region_name: 17
source: dbSNP
start: 73408264
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1248748147
seq_region_name: 17
source: dbSNP
start: 73408271
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1418692928
seq_region_name: 17
source: dbSNP
start: 73408274
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs8068583
seq_region_name: 17
source: dbSNP
start: 73408280
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1026081958
seq_region_name: 17
source: dbSNP
start: 73408282
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408287
feature_type: variation
id: rs2063097353
seq_region_name: 17
source: dbSNP
start: 73408287
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs556422990
seq_region_name: 17
source: dbSNP
start: 73408293
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs887576857
seq_region_name: 17
source: dbSNP
start: 73408294
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408300
feature_type: variation
id: rs2063097437
seq_region_name: 17
source: dbSNP
start: 73408300
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1425540872
seq_region_name: 17
source: dbSNP
start: 73408302
strand: 1
-
alleles:
- GCCTCCCGGG
- GCCTCCCGGGATCACGCCATTCTCCGCCTCCCGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408313
feature_type: variation
id: rs1417266097
seq_region_name: 17
source: dbSNP
start: 73408304
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408306
feature_type: variation
id: rs1006057736
seq_region_name: 17
source: dbSNP
start: 73408306
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1466783496
seq_region_name: 17
source: dbSNP
start: 73408310
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408311
feature_type: variation
id: rs560135668
seq_region_name: 17
source: dbSNP
start: 73408311
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408312
feature_type: variation
id: rs1599535681
seq_region_name: 17
source: dbSNP
start: 73408312
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1395373205
seq_region_name: 17
source: dbSNP
start: 73408318
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408319
feature_type: variation
id: rs1490297016
seq_region_name: 17
source: dbSNP
start: 73408319
strand: 1
-
alleles:
- T
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- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs8073252
seq_region_name: 17
source: dbSNP
start: 73408322
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408329
feature_type: variation
id: rs2063097729
seq_region_name: 17
source: dbSNP
start: 73408325
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408327
feature_type: variation
id: rs1306307850
seq_region_name: 17
source: dbSNP
start: 73408327
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408330
feature_type: variation
id: rs2145550764
seq_region_name: 17
source: dbSNP
start: 73408330
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408331
feature_type: variation
id: rs1295481285
seq_region_name: 17
source: dbSNP
start: 73408331
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599535718
seq_region_name: 17
source: dbSNP
start: 73408332
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408337
feature_type: variation
id: rs1302433715
seq_region_name: 17
source: dbSNP
start: 73408337
strand: 1
-
alleles:
- CCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1361959779
seq_region_name: 17
source: dbSNP
start: 73408340
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408342
feature_type: variation
id: rs1279734268
seq_region_name: 17
source: dbSNP
start: 73408342
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408343
feature_type: variation
id: rs1347705783
seq_region_name: 17
source: dbSNP
start: 73408343
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408347
feature_type: variation
id: rs1222065346
seq_region_name: 17
source: dbSNP
start: 73408347
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408349
feature_type: variation
id: rs1402666581
seq_region_name: 17
source: dbSNP
start: 73408349
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408350
feature_type: variation
id: rs992065954
seq_region_name: 17
source: dbSNP
start: 73408350
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408357
feature_type: variation
id: rs1319187225
seq_region_name: 17
source: dbSNP
start: 73408357
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408360
feature_type: variation
id: rs2145550843
seq_region_name: 17
source: dbSNP
start: 73408360
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408364
feature_type: variation
id: rs1024915715
seq_region_name: 17
source: dbSNP
start: 73408364
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408366
feature_type: variation
id: rs2063098026
seq_region_name: 17
source: dbSNP
start: 73408366
strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408367
feature_type: variation
id: rs2063098046
seq_region_name: 17
source: dbSNP
start: 73408367
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408372
feature_type: variation
id: rs1220589803
seq_region_name: 17
source: dbSNP
start: 73408372
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408373
feature_type: variation
id: rs2063098106
seq_region_name: 17
source: dbSNP
start: 73408373
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408374
feature_type: variation
id: rs1401968520
seq_region_name: 17
source: dbSNP
start: 73408374
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408375
feature_type: variation
id: rs966702886
seq_region_name: 17
source: dbSNP
start: 73408375
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408382
feature_type: variation
id: rs2063098170
seq_region_name: 17
source: dbSNP
start: 73408377
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408378
feature_type: variation
id: rs2063098196
seq_region_name: 17
source: dbSNP
start: 73408378
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408380
feature_type: variation
id: rs2063098214
seq_region_name: 17
source: dbSNP
start: 73408380
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408381
feature_type: variation
id: rs1480442853
seq_region_name: 17
source: dbSNP
start: 73408381
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408382
feature_type: variation
id: rs2063098268
seq_region_name: 17
source: dbSNP
start: 73408382
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408383
feature_type: variation
id: rs2063098297
seq_region_name: 17
source: dbSNP
start: 73408383
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408384
feature_type: variation
id: rs1568387079
seq_region_name: 17
source: dbSNP
start: 73408384
strand: 1
-
alleles:
- TTTTTTTTTTTTT
- TTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408396
feature_type: variation
id: rs538704048
seq_region_name: 17
source: dbSNP
start: 73408384
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408385
feature_type: variation
id: rs2063098434
seq_region_name: 17
source: dbSNP
start: 73408385
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408388
feature_type: variation
id: rs1269831816
seq_region_name: 17
source: dbSNP
start: 73408388
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408508
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408511
strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063099827
seq_region_name: 17
source: dbSNP
start: 73408515
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73408517
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73408519
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs928968587
seq_region_name: 17
source: dbSNP
start: 73408520
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408521
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408521
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408523
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408524
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408525
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408528
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1019700438
seq_region_name: 17
source: dbSNP
start: 73408532
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs965285635
seq_region_name: 17
source: dbSNP
start: 73408537
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73408542
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73408543
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408544
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063100200
seq_region_name: 17
source: dbSNP
start: 73408549
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1183451324
seq_region_name: 17
source: dbSNP
start: 73408552
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs972679666
seq_region_name: 17
source: dbSNP
start: 73408554
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1282696871
seq_region_name: 17
source: dbSNP
start: 73408555
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1256185613
seq_region_name: 17
source: dbSNP
start: 73408562
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408565
feature_type: variation
id: rs1245604960
seq_region_name: 17
source: dbSNP
start: 73408565
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73408568
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063100346
seq_region_name: 17
source: dbSNP
start: 73408570
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408571
feature_type: variation
id: rs553870796
seq_region_name: 17
source: dbSNP
start: 73408571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408576
feature_type: variation
id: rs1484712989
seq_region_name: 17
source: dbSNP
start: 73408576
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408578
feature_type: variation
id: rs1294294295
seq_region_name: 17
source: dbSNP
start: 73408578
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408586
feature_type: variation
id: rs2063100433
seq_region_name: 17
source: dbSNP
start: 73408586
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408591
feature_type: variation
id: rs918408316
seq_region_name: 17
source: dbSNP
start: 73408591
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408593
feature_type: variation
id: rs2063100489
seq_region_name: 17
source: dbSNP
start: 73408593
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-
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-
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73408701
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408711
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73408717
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73408717
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408718
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408724
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408726
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73408726
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408726
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408728
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408731
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408732
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408733
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73408734
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs999533945
seq_region_name: 17
source: dbSNP
start: 73408735
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063102021
seq_region_name: 17
source: dbSNP
start: 73408746
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs760312879
seq_region_name: 17
source: dbSNP
start: 73408747
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408750
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408759
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408762
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1423563422
seq_region_name: 17
source: dbSNP
start: 73408763
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1361507177
seq_region_name: 17
source: dbSNP
start: 73408766
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1163370361
seq_region_name: 17
source: dbSNP
start: 73408766
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs879930484
seq_region_name: 17
source: dbSNP
start: 73408767
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs889503094
seq_region_name: 17
source: dbSNP
start: 73408769
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145552097
seq_region_name: 17
source: dbSNP
start: 73408771
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408781
feature_type: variation
id: rs540289405
seq_region_name: 17
source: dbSNP
start: 73408774
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408781
feature_type: variation
id: rs965554423
seq_region_name: 17
source: dbSNP
start: 73408781
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408782
feature_type: variation
id: rs1007089649
seq_region_name: 17
source: dbSNP
start: 73408782
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408789
feature_type: variation
id: rs2063102377
seq_region_name: 17
source: dbSNP
start: 73408789
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408791
feature_type: variation
id: rs1019267516
seq_region_name: 17
source: dbSNP
start: 73408791
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408792
feature_type: variation
id: rs2063102434
seq_region_name: 17
source: dbSNP
start: 73408792
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408795
feature_type: variation
id: rs965069938
seq_region_name: 17
source: dbSNP
start: 73408795
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408797
feature_type: variation
id: rs1722356656
seq_region_name: 17
source: dbSNP
start: 73408797
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408799
feature_type: variation
id: rs2063102479
seq_region_name: 17
source: dbSNP
start: 73408799
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408803
feature_type: variation
id: rs1396724600
seq_region_name: 17
source: dbSNP
start: 73408803
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408804
feature_type: variation
id: rs994066396
seq_region_name: 17
source: dbSNP
start: 73408804
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408807
feature_type: variation
id: rs759177797
seq_region_name: 17
source: dbSNP
start: 73408807
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408809
feature_type: variation
id: rs544850071
seq_region_name: 17
source: dbSNP
start: 73408809
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408815
feature_type: variation
id: rs1282869824
seq_region_name: 17
source: dbSNP
start: 73408815
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408818
feature_type: variation
id: rs1437646115
seq_region_name: 17
source: dbSNP
start: 73408818
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408819
feature_type: variation
id: rs1599536307
seq_region_name: 17
source: dbSNP
start: 73408819
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408821
feature_type: variation
id: rs952619803
seq_region_name: 17
source: dbSNP
start: 73408821
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408823
feature_type: variation
id: rs2063102703
seq_region_name: 17
source: dbSNP
start: 73408823
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408828
feature_type: variation
id: rs983932612
seq_region_name: 17
source: dbSNP
start: 73408828
strand: 1
-
alleles:
- AAATAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408835
feature_type: variation
id: rs1446937356
seq_region_name: 17
source: dbSNP
start: 73408829
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408830
feature_type: variation
id: rs1245456747
seq_region_name: 17
source: dbSNP
start: 73408830
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408832
feature_type: variation
id: rs556483897
seq_region_name: 17
source: dbSNP
start: 73408832
strand: 1
-
alleles:
- AAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408836
feature_type: variation
id: rs1391371735
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73408835
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063103035
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1318429110
seq_region_name: 17
source: dbSNP
start: 73408854
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs373739044
seq_region_name: 17
source: dbSNP
start: 73408856
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs879275495
seq_region_name: 17
source: dbSNP
start: 73408857
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103146
seq_region_name: 17
source: dbSNP
start: 73408859
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103162
seq_region_name: 17
source: dbSNP
start: 73408860
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103216
seq_region_name: 17
source: dbSNP
start: 73408869
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1260127904
seq_region_name: 17
source: dbSNP
start: 73408879
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1437210225
seq_region_name: 17
source: dbSNP
start: 73408881
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1483520133
seq_region_name: 17
source: dbSNP
start: 73408884
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103309
seq_region_name: 17
source: dbSNP
start: 73408889
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1238710537
seq_region_name: 17
source: dbSNP
start: 73408891
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1200668421
seq_region_name: 17
source: dbSNP
start: 73408895
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1055303622
seq_region_name: 17
source: dbSNP
start: 73408896
strand: 1
-
alleles:
- GATATTACAGGG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408907
feature_type: variation
id: rs754524793
seq_region_name: 17
source: dbSNP
start: 73408896
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1219986033
seq_region_name: 17
source: dbSNP
start: 73408903
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1278184461
seq_region_name: 17
source: dbSNP
start: 73408908
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1238771480
seq_region_name: 17
source: dbSNP
start: 73408914
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103523
seq_region_name: 17
source: dbSNP
start: 73408924
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1378364850
seq_region_name: 17
source: dbSNP
start: 73408926
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs993350370
seq_region_name: 17
source: dbSNP
start: 73408927
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs186934108
seq_region_name: 17
source: dbSNP
start: 73408928
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103618
seq_region_name: 17
source: dbSNP
start: 73408931
strand: 1
-
alleles:
- ATGAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1448354308
seq_region_name: 17
source: dbSNP
start: 73408933
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs760299898
seq_region_name: 17
source: dbSNP
start: 73408942
strand: 1
-
alleles:
- A
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2133273
seq_region_name: 17
source: dbSNP
start: 73408943
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103731
seq_region_name: 17
source: dbSNP
start: 73408943
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs926175018
seq_region_name: 17
source: dbSNP
start: 73408945
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103772
seq_region_name: 17
source: dbSNP
start: 73408949
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73408950
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063103818
seq_region_name: 17
source: dbSNP
start: 73408951
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408952
feature_type: variation
id: rs2063103849
seq_region_name: 17
source: dbSNP
start: 73408952
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1156668601
seq_region_name: 17
source: dbSNP
start: 73408962
strand: 1
-
alleles:
- TAAATA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1402865925
seq_region_name: 17
source: dbSNP
start: 73408962
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs879187765
seq_region_name: 17
source: dbSNP
start: 73408964
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs936258923
seq_region_name: 17
source: dbSNP
start: 73408966
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408972
feature_type: variation
id: rs1050612108
seq_region_name: 17
source: dbSNP
start: 73408972
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408975
feature_type: variation
id: rs2063103974
seq_region_name: 17
source: dbSNP
start: 73408975
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408993
feature_type: variation
id: rs902434531
seq_region_name: 17
source: dbSNP
start: 73408993
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408994
feature_type: variation
id: rs889315622
seq_region_name: 17
source: dbSNP
start: 73408994
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73408996
feature_type: variation
id: rs999881970
seq_region_name: 17
source: dbSNP
start: 73408996
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409001
feature_type: variation
id: rs2063104068
seq_region_name: 17
source: dbSNP
start: 73409001
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409006
feature_type: variation
id: rs1442890401
seq_region_name: 17
source: dbSNP
start: 73409006
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409008
feature_type: variation
id: rs2063104124
seq_region_name: 17
source: dbSNP
start: 73409008
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409009
feature_type: variation
id: rs1032328847
seq_region_name: 17
source: dbSNP
start: 73409009
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409013
feature_type: variation
id: rs2063104168
seq_region_name: 17
source: dbSNP
start: 73409013
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409014
feature_type: variation
id: rs2063104194
seq_region_name: 17
source: dbSNP
start: 73409014
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409018
feature_type: variation
id: rs2063104222
seq_region_name: 17
source: dbSNP
start: 73409018
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409020
feature_type: variation
id: rs1599536473
seq_region_name: 17
source: dbSNP
start: 73409020
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409021
feature_type: variation
id: rs1444413488
seq_region_name: 17
source: dbSNP
start: 73409021
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409026
feature_type: variation
id: rs2063104306
seq_region_name: 17
source: dbSNP
start: 73409026
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409029
feature_type: variation
id: rs1157347403
seq_region_name: 17
source: dbSNP
start: 73409028
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409031
feature_type: variation
id: rs2063104334
seq_region_name: 17
source: dbSNP
start: 73409031
strand: 1
-
alleles:
- TTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409034
feature_type: variation
id: rs1345158923
seq_region_name: 17
source: dbSNP
start: 73409032
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409041
feature_type: variation
id: rs2063104378
seq_region_name: 17
source: dbSNP
start: 73409041
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409043
feature_type: variation
id: rs2063104406
seq_region_name: 17
source: dbSNP
start: 73409043
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409045
feature_type: variation
id: rs2063104433
seq_region_name: 17
source: dbSNP
start: 73409045
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409051
feature_type: variation
id: rs2145552666
seq_region_name: 17
source: dbSNP
start: 73409051
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409058
feature_type: variation
id: rs1568387412
seq_region_name: 17
source: dbSNP
start: 73409058
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409059
feature_type: variation
id: rs1204928254
seq_region_name: 17
source: dbSNP
start: 73409059
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409067
feature_type: variation
id: rs760338180
seq_region_name: 17
source: dbSNP
start: 73409067
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409075
feature_type: variation
id: rs1312134423
seq_region_name: 17
source: dbSNP
start: 73409075
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409076
feature_type: variation
id: rs1599536516
seq_region_name: 17
source: dbSNP
start: 73409076
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409079
feature_type: variation
id: rs1006626258
seq_region_name: 17
source: dbSNP
start: 73409079
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409081
feature_type: variation
id: rs1568387425
seq_region_name: 17
source: dbSNP
start: 73409081
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409086
feature_type: variation
id: rs1041216220
seq_region_name: 17
source: dbSNP
start: 73409086
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409088
feature_type: variation
id: rs1018383981
seq_region_name: 17
source: dbSNP
start: 73409088
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409089
feature_type: variation
id: rs2063104718
seq_region_name: 17
source: dbSNP
start: 73409089
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409092
feature_type: variation
id: rs1283136483
seq_region_name: 17
source: dbSNP
start: 73409092
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409093
feature_type: variation
id: rs2063104760
seq_region_name: 17
source: dbSNP
start: 73409093
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409100
feature_type: variation
id: rs1448120080
seq_region_name: 17
source: dbSNP
start: 73409100
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409102
feature_type: variation
id: rs1360598732
seq_region_name: 17
source: dbSNP
start: 73409102
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409103
feature_type: variation
id: rs542650712
seq_region_name: 17
source: dbSNP
start: 73409103
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409108
feature_type: variation
id: rs2145552765
seq_region_name: 17
source: dbSNP
start: 73409108
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409121
feature_type: variation
id: rs2145552773
seq_region_name: 17
source: dbSNP
start: 73409121
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409123
feature_type: variation
id: rs1315720781
seq_region_name: 17
source: dbSNP
start: 73409123
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409128
feature_type: variation
id: rs570934496
seq_region_name: 17
source: dbSNP
start: 73409128
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs753343471
seq_region_name: 17
source: dbSNP
start: 73409132
strand: 1
-
alleles:
- AGGTGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409137
feature_type: variation
id: rs2063104917
seq_region_name: 17
source: dbSNP
start: 73409132
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1452192060
seq_region_name: 17
source: dbSNP
start: 73409135
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063104972
seq_region_name: 17
source: dbSNP
start: 73409144
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs376858097
seq_region_name: 17
source: dbSNP
start: 73409147
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1375778938
seq_region_name: 17
source: dbSNP
start: 73409157
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409158
feature_type: variation
id: rs976920590
seq_region_name: 17
source: dbSNP
start: 73409158
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409160
feature_type: variation
id: rs1412969981
seq_region_name: 17
source: dbSNP
start: 73409160
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409161
feature_type: variation
id: rs1182576778
seq_region_name: 17
source: dbSNP
start: 73409161
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409163
feature_type: variation
id: rs952605347
seq_region_name: 17
source: dbSNP
start: 73409163
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409164
feature_type: variation
id: rs2063105098
seq_region_name: 17
source: dbSNP
start: 73409164
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1240578720
seq_region_name: 17
source: dbSNP
start: 73409171
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409186
feature_type: variation
id: rs2063105147
seq_region_name: 17
source: dbSNP
start: 73409186
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409188
feature_type: variation
id: rs1192689237
seq_region_name: 17
source: dbSNP
start: 73409187
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409188
feature_type: variation
id: rs2063105167
seq_region_name: 17
source: dbSNP
start: 73409188
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409189
feature_type: variation
id: rs1488832461
seq_region_name: 17
source: dbSNP
start: 73409189
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409194
feature_type: variation
id: rs2063105228
seq_region_name: 17
source: dbSNP
start: 73409194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409202
feature_type: variation
id: rs2063105249
seq_region_name: 17
source: dbSNP
start: 73409202
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409203
feature_type: variation
id: rs1005917428
seq_region_name: 17
source: dbSNP
start: 73409203
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409206
feature_type: variation
id: rs1359444352
seq_region_name: 17
source: dbSNP
start: 73409206
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409207
feature_type: variation
id: rs2063105348
seq_region_name: 17
source: dbSNP
start: 73409207
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409209
feature_type: variation
id: rs2063105371
seq_region_name: 17
source: dbSNP
start: 73409209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409212
feature_type: variation
id: rs2063105399
seq_region_name: 17
source: dbSNP
start: 73409212
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409215
feature_type: variation
id: rs1291204489
seq_region_name: 17
source: dbSNP
start: 73409215
strand: 1
-
alleles:
- CACGCCTATAATGCCAGCAC
- CAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409235
feature_type: variation
id: rs1228410201
seq_region_name: 17
source: dbSNP
start: 73409216
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409218
feature_type: variation
id: rs146975182
seq_region_name: 17
source: dbSNP
start: 73409218
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409219
feature_type: variation
id: rs958812711
seq_region_name: 17
source: dbSNP
start: 73409219
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409220
feature_type: variation
id: rs1268078288
seq_region_name: 17
source: dbSNP
start: 73409220
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409224
feature_type: variation
id: rs2063105531
seq_region_name: 17
source: dbSNP
start: 73409224
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409225
feature_type: variation
id: rs550289301
seq_region_name: 17
source: dbSNP
start: 73409225
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409226
feature_type: variation
id: rs2063105550
seq_region_name: 17
source: dbSNP
start: 73409226
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409230
feature_type: variation
id: rs570125981
seq_region_name: 17
source: dbSNP
start: 73409230
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409232
feature_type: variation
id: rs1460541619
seq_region_name: 17
source: dbSNP
start: 73409232
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409233
feature_type: variation
id: rs1299877374
seq_region_name: 17
source: dbSNP
start: 73409233
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409237
feature_type: variation
id: rs2063105640
seq_region_name: 17
source: dbSNP
start: 73409237
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409240
feature_type: variation
id: rs1422497927
seq_region_name: 17
source: dbSNP
start: 73409240
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409243
feature_type: variation
id: rs2063105702
seq_region_name: 17
source: dbSNP
start: 73409243
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409249
feature_type: variation
id: rs941707287
seq_region_name: 17
source: dbSNP
start: 73409249
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409250
feature_type: variation
id: rs879902940
seq_region_name: 17
source: dbSNP
start: 73409250
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409251
feature_type: variation
id: rs1599536645
seq_region_name: 17
source: dbSNP
start: 73409251
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409254
feature_type: variation
id: rs1234302352
seq_region_name: 17
source: dbSNP
start: 73409254
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409256
feature_type: variation
id: rs1024316817
seq_region_name: 17
source: dbSNP
start: 73409256
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409258
feature_type: variation
id: rs1170036270
seq_region_name: 17
source: dbSNP
start: 73409258
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409260
feature_type: variation
id: rs2063105885
seq_region_name: 17
source: dbSNP
start: 73409260
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409267
feature_type: variation
id: rs2063105903
seq_region_name: 17
source: dbSNP
start: 73409267
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409279
feature_type: variation
id: rs1478296747
seq_region_name: 17
source: dbSNP
start: 73409279
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409282
feature_type: variation
id: rs12938226
seq_region_name: 17
source: dbSNP
start: 73409282
strand: 1
-
alleles:
- CC
- CCTGGTCAACGTGGTGAAACCCCAGGTGGATCATTTGAGGTCAGGAGTTTGAGACC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409284
feature_type: variation
id: rs1568387506
seq_region_name: 17
source: dbSNP
start: 73409283
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409284
feature_type: variation
id: rs1488327680
seq_region_name: 17
source: dbSNP
start: 73409284
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409293
feature_type: variation
id: rs2063106061
seq_region_name: 17
source: dbSNP
start: 73409293
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409294
feature_type: variation
id: rs1568387514
seq_region_name: 17
source: dbSNP
start: 73409294
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409296
feature_type: variation
id: rs7503469
seq_region_name: 17
source: dbSNP
start: 73409296
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409297
feature_type: variation
id: rs1434266433
seq_region_name: 17
source: dbSNP
start: 73409297
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409306
feature_type: variation
id: rs2063106173
seq_region_name: 17
source: dbSNP
start: 73409306
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409308
feature_type: variation
id: rs949175805
seq_region_name: 17
source: dbSNP
start: 73409308
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409309
feature_type: variation
id: rs778300737
seq_region_name: 17
source: dbSNP
start: 73409309
strand: 1
-
alleles:
- CAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409311
feature_type: variation
id: rs1179122089
seq_region_name: 17
source: dbSNP
start: 73409309
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409317
feature_type: variation
id: rs146125424
seq_region_name: 17
source: dbSNP
start: 73409317
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409326
feature_type: variation
id: rs1279634916
seq_region_name: 17
source: dbSNP
start: 73409326
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409331
feature_type: variation
id: rs2063106333
seq_region_name: 17
source: dbSNP
start: 73409331
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409331
feature_type: variation
id: rs2063106355
seq_region_name: 17
source: dbSNP
start: 73409332
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409333
feature_type: variation
id: rs2145553159
seq_region_name: 17
source: dbSNP
start: 73409333
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409337
feature_type: variation
id: rs757519766
seq_region_name: 17
source: dbSNP
start: 73409337
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409338
feature_type: variation
id: rs781626959
seq_region_name: 17
source: dbSNP
start: 73409338
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409341
feature_type: variation
id: rs1568387547
seq_region_name: 17
source: dbSNP
start: 73409341
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409343
feature_type: variation
id: rs1469402932
seq_region_name: 17
source: dbSNP
start: 73409343
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409348
feature_type: variation
id: rs2063106509
seq_region_name: 17
source: dbSNP
start: 73409348
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409349
feature_type: variation
id: rs551392431
seq_region_name: 17
source: dbSNP
start: 73409349
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409350
feature_type: variation
id: rs1294062868
seq_region_name: 17
source: dbSNP
start: 73409350
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409351
feature_type: variation
id: rs2063106557
seq_region_name: 17
source: dbSNP
start: 73409351
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409353
feature_type: variation
id: rs2063106588
seq_region_name: 17
source: dbSNP
start: 73409353
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409354
feature_type: variation
id: rs2063106616
seq_region_name: 17
source: dbSNP
start: 73409354
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409356
feature_type: variation
id: rs2063106641
seq_region_name: 17
source: dbSNP
start: 73409356
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409362
feature_type: variation
id: rs2063106665
seq_region_name: 17
source: dbSNP
start: 73409362
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409363
feature_type: variation
id: rs910702092
seq_region_name: 17
source: dbSNP
start: 73409363
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409373
feature_type: variation
id: rs9906860
seq_region_name: 17
source: dbSNP
start: 73409373
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409374
feature_type: variation
id: rs1352663576
seq_region_name: 17
source: dbSNP
start: 73409374
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409386
feature_type: variation
id: rs2063106752
seq_region_name: 17
source: dbSNP
start: 73409386
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409389
feature_type: variation
id: rs2063106773
seq_region_name: 17
source: dbSNP
start: 73409389
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409391
feature_type: variation
id: rs935242308
seq_region_name: 17
source: dbSNP
start: 73409391
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409396
feature_type: variation
id: rs2145553269
seq_region_name: 17
source: dbSNP
start: 73409396
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409399
feature_type: variation
id: rs1356529579
seq_region_name: 17
source: dbSNP
start: 73409399
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409401
feature_type: variation
id: rs2063106824
seq_region_name: 17
source: dbSNP
start: 73409401
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409402
feature_type: variation
id: rs2063106846
seq_region_name: 17
source: dbSNP
start: 73409402
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409403
feature_type: variation
id: rs1568387570
seq_region_name: 17
source: dbSNP
start: 73409403
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409408
feature_type: variation
id: rs2063106882
seq_region_name: 17
source: dbSNP
start: 73409408
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409410
feature_type: variation
id: rs1426071047
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-
alleles:
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-
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alleles:
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alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73409559
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1380181959
seq_region_name: 17
source: dbSNP
start: 73409565
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409570
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1304738613
seq_region_name: 17
source: dbSNP
start: 73409574
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409576
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409579
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409582
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs949124370
seq_region_name: 17
source: dbSNP
start: 73409586
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409587
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409588
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063108600
seq_region_name: 17
source: dbSNP
start: 73409592
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73409594
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409599
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409603
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409604
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs923771986
seq_region_name: 17
source: dbSNP
start: 73409605
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1427868568
seq_region_name: 17
source: dbSNP
start: 73409609
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1480374492
seq_region_name: 17
source: dbSNP
start: 73409610
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145553802
seq_region_name: 17
source: dbSNP
start: 73409611
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409612
feature_type: variation
id: rs1168594174
seq_region_name: 17
source: dbSNP
start: 73409612
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409620
feature_type: variation
id: rs2063108843
seq_region_name: 17
source: dbSNP
start: 73409620
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409622
feature_type: variation
id: rs1487199043
seq_region_name: 17
source: dbSNP
start: 73409622
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409624
feature_type: variation
id: rs2063108900
seq_region_name: 17
source: dbSNP
start: 73409624
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409625
feature_type: variation
id: rs2063108924
seq_region_name: 17
source: dbSNP
start: 73409625
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409626
feature_type: variation
id: rs935174712
seq_region_name: 17
source: dbSNP
start: 73409626
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409629
feature_type: variation
id: rs1421669938
seq_region_name: 17
source: dbSNP
start: 73409629
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409630
feature_type: variation
id: rs2063108993
seq_region_name: 17
source: dbSNP
start: 73409630
strand: 1
-
alleles:
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- AAAAAAA
- AAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409638
feature_type: variation
id: rs1053675573
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-
alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409782
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409784
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409791
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409796
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73409798
feature_type: variation
id: rs2063110569
seq_region_name: 17
source: dbSNP
start: 73409798
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs548240379
seq_region_name: 17
source: dbSNP
start: 73409799
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73409800
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145554399
seq_region_name: 17
source: dbSNP
start: 73409804
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs989716446
seq_region_name: 17
source: dbSNP
start: 73409805
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063110664
seq_region_name: 17
source: dbSNP
start: 73409809
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1161467838
seq_region_name: 17
source: dbSNP
start: 73409812
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1258986710
seq_region_name: 17
source: dbSNP
start: 73409815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs957488866
seq_region_name: 17
source: dbSNP
start: 73409816
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409817
feature_type: variation
id: rs1200711744
seq_region_name: 17
source: dbSNP
start: 73409817
strand: 1
-
alleles:
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- TCTCTCTCTCTCTCTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409832
feature_type: variation
id: rs915109554
seq_region_name: 17
source: dbSNP
start: 73409818
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1039661497
seq_region_name: 17
source: dbSNP
start: 73409819
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409821
feature_type: variation
id: rs76116052
seq_region_name: 17
source: dbSNP
start: 73409821
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409823
feature_type: variation
id: rs1599537277
seq_region_name: 17
source: dbSNP
start: 73409823
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409825
feature_type: variation
id: rs2063110909
seq_region_name: 17
source: dbSNP
start: 73409825
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409828
feature_type: variation
id: rs1320282921
seq_region_name: 17
source: dbSNP
start: 73409828
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409834
feature_type: variation
id: rs2063110964
seq_region_name: 17
source: dbSNP
start: 73409830
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73409908
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73409910
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73409916
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409924
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409930
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409937
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409939
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409944
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73409945
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73409958
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409960
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409961
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409966
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73409967
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409969
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409975
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409978
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73409981
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063112867
seq_region_name: 17
source: dbSNP
start: 73409987
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73409993
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73409997
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seq_region_name: 17
source: dbSNP
start: 73409997
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003164351
seq_region_name: 17
source: dbSNP
start: 73410000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410001
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410001
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73410211
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73410240
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73410250
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73410266
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73410275
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410277
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73410278
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73410283
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73410288
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73410292
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410294
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410340
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410354
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410357
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410367
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410374
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73410375
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410377
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410378
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410382
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410389
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410391
strand: 1
-
alleles:
- AA
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410393
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410395
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs529862631
seq_region_name: 17
source: dbSNP
start: 73410396
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867373777
seq_region_name: 17
source: dbSNP
start: 73410399
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73410400
feature_type: variation
id: rs2063116016
seq_region_name: 17
source: dbSNP
start: 73410400
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410402
feature_type: variation
id: rs1199852677
seq_region_name: 17
source: dbSNP
start: 73410402
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410403
feature_type: variation
id: rs2063116101
seq_region_name: 17
source: dbSNP
start: 73410403
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410405
feature_type: variation
id: rs2063116119
seq_region_name: 17
source: dbSNP
start: 73410405
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1301249447
seq_region_name: 17
source: dbSNP
start: 73410406
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410406
feature_type: variation
id: rs1465883953
seq_region_name: 17
source: dbSNP
start: 73410406
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410411
feature_type: variation
id: rs2145556008
seq_region_name: 17
source: dbSNP
start: 73410411
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1360156061
seq_region_name: 17
source: dbSNP
start: 73410414
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410416
feature_type: variation
id: rs548014552
seq_region_name: 17
source: dbSNP
start: 73410416
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs749426562
seq_region_name: 17
source: dbSNP
start: 73410417
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410419
feature_type: variation
id: rs2063116291
seq_region_name: 17
source: dbSNP
start: 73410419
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410423
feature_type: variation
id: rs1175113526
seq_region_name: 17
source: dbSNP
start: 73410423
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410426
feature_type: variation
id: rs901942003
seq_region_name: 17
source: dbSNP
start: 73410426
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063116371
seq_region_name: 17
source: dbSNP
start: 73410427
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410430
feature_type: variation
id: rs563373727
seq_region_name: 17
source: dbSNP
start: 73410430
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410431
feature_type: variation
id: rs2063116413
seq_region_name: 17
source: dbSNP
start: 73410431
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410437
feature_type: variation
id: rs1419077431
seq_region_name: 17
source: dbSNP
start: 73410437
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410438
feature_type: variation
id: rs185346697
seq_region_name: 17
source: dbSNP
start: 73410438
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410439
feature_type: variation
id: rs2063116497
seq_region_name: 17
source: dbSNP
start: 73410439
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410440
feature_type: variation
id: rs975244393
seq_region_name: 17
source: dbSNP
start: 73410440
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410443
feature_type: variation
id: rs2063116545
seq_region_name: 17
source: dbSNP
start: 73410443
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410459
feature_type: variation
id: rs2145556082
seq_region_name: 17
source: dbSNP
start: 73410459
strand: 1
-
alleles:
- TGTGTGT
- TGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410468
feature_type: variation
id: rs922464524
seq_region_name: 17
source: dbSNP
start: 73410462
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410472
feature_type: variation
id: rs1258016410
seq_region_name: 17
source: dbSNP
start: 73410472
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410476
feature_type: variation
id: rs190538502
seq_region_name: 17
source: dbSNP
start: 73410476
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410477
feature_type: variation
id: rs1351500586
seq_region_name: 17
source: dbSNP
start: 73410477
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410478
feature_type: variation
id: rs1409647931
seq_region_name: 17
source: dbSNP
start: 73410478
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410480
feature_type: variation
id: rs113363250
seq_region_name: 17
source: dbSNP
start: 73410480
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410482
feature_type: variation
id: rs1239868105
seq_region_name: 17
source: dbSNP
start: 73410482
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410486
feature_type: variation
id: rs1318770217
seq_region_name: 17
source: dbSNP
start: 73410486
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410490
feature_type: variation
id: rs139478031
seq_region_name: 17
source: dbSNP
start: 73410490
strand: 1
-
alleles:
- TATT
- TATTATT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410494
feature_type: variation
id: rs1310877305
seq_region_name: 17
source: dbSNP
start: 73410491
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410496
feature_type: variation
id: rs2063116777
seq_region_name: 17
source: dbSNP
start: 73410496
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410498
feature_type: variation
id: rs1380153891
seq_region_name: 17
source: dbSNP
start: 73410498
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410500
feature_type: variation
id: rs2063116817
seq_region_name: 17
source: dbSNP
start: 73410500
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410503
feature_type: variation
id: rs2063116831
seq_region_name: 17
source: dbSNP
start: 73410503
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
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-
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73410619
strand: 1
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alleles:
- TGCTGCTTCTTAGAGTCCCTGTGCTGCTT
- TGCTGCTT
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73410660
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73410661
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73410668
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410672
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410675
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410677
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410680
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410683
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410686
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410687
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410694
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410703
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063118330
seq_region_name: 17
source: dbSNP
start: 73410704
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410705
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410708
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410711
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1271209391
seq_region_name: 17
source: dbSNP
start: 73410713
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063118423
seq_region_name: 17
source: dbSNP
start: 73410713
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410717
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063118463
seq_region_name: 17
source: dbSNP
start: 73410718
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145556697
seq_region_name: 17
source: dbSNP
start: 73410723
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1230056190
seq_region_name: 17
source: dbSNP
start: 73410724
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1329870677
seq_region_name: 17
source: dbSNP
start: 73410726
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063118498
seq_region_name: 17
source: dbSNP
start: 73410732
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410737
feature_type: variation
id: rs2063118516
seq_region_name: 17
source: dbSNP
start: 73410737
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410739
feature_type: variation
id: rs80283036
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- CA
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410900
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063120170
seq_region_name: 17
source: dbSNP
start: 73410902
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410907
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410908
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1443860513
seq_region_name: 17
source: dbSNP
start: 73410908
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73410914
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1015516787
seq_region_name: 17
source: dbSNP
start: 73410918
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs895398351
seq_region_name: 17
source: dbSNP
start: 73410921
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs145125795
seq_region_name: 17
source: dbSNP
start: 73410922
strand: 1
-
alleles:
- GGGGG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs962993870
seq_region_name: 17
source: dbSNP
start: 73410922
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1246910511
seq_region_name: 17
source: dbSNP
start: 73410925
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1293677894
seq_region_name: 17
source: dbSNP
start: 73410928
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1156947063
seq_region_name: 17
source: dbSNP
start: 73410930
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1439091887
seq_region_name: 17
source: dbSNP
start: 73410931
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063120736
seq_region_name: 17
source: dbSNP
start: 73410932
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063120774
seq_region_name: 17
source: dbSNP
start: 73410936
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs147625151
seq_region_name: 17
source: dbSNP
start: 73410938
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063120874
seq_region_name: 17
source: dbSNP
start: 73410943
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73410944
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063120945
seq_region_name: 17
source: dbSNP
start: 73410950
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410952
feature_type: variation
id: rs865988212
seq_region_name: 17
source: dbSNP
start: 73410952
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs142151463
seq_region_name: 17
source: dbSNP
start: 73410964
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410966
feature_type: variation
id: rs934853800
seq_region_name: 17
source: dbSNP
start: 73410966
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410974
feature_type: variation
id: rs2063121047
seq_region_name: 17
source: dbSNP
start: 73410974
strand: 1
-
alleles:
- TT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410981
feature_type: variation
id: rs1053741433
seq_region_name: 17
source: dbSNP
start: 73410980
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410981
feature_type: variation
id: rs1350696288
seq_region_name: 17
source: dbSNP
start: 73410981
strand: 1
-
alleles:
- TGTG
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410984
feature_type: variation
id: rs1261287996
seq_region_name: 17
source: dbSNP
start: 73410981
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410984
feature_type: variation
id: rs1599538464
seq_region_name: 17
source: dbSNP
start: 73410984
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410991
feature_type: variation
id: rs2063121234
seq_region_name: 17
source: dbSNP
start: 73410991
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410993
feature_type: variation
id: rs1031280771
seq_region_name: 17
source: dbSNP
start: 73410993
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs955710754
seq_region_name: 17
source: dbSNP
start: 73410994
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410995
feature_type: variation
id: rs2063121314
seq_region_name: 17
source: dbSNP
start: 73410995
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73410997
feature_type: variation
id: rs990236035
seq_region_name: 17
source: dbSNP
start: 73410997
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411000
feature_type: variation
id: rs2145557213
seq_region_name: 17
source: dbSNP
start: 73411000
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411002
feature_type: variation
id: rs1599538480
seq_region_name: 17
source: dbSNP
start: 73411002
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411006
feature_type: variation
id: rs914460825
seq_region_name: 17
source: dbSNP
start: 73411006
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411007
feature_type: variation
id: rs893388081
seq_region_name: 17
source: dbSNP
start: 73411007
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411008
feature_type: variation
id: rs947663678
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73411018
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063121576
seq_region_name: 17
source: dbSNP
start: 73411026
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063121605
seq_region_name: 17
source: dbSNP
start: 73411027
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411029
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73411040
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1674444186
seq_region_name: 17
source: dbSNP
start: 73411041
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs756618027
seq_region_name: 17
source: dbSNP
start: 73411045
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs899524885
seq_region_name: 17
source: dbSNP
start: 73411047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs923135751
seq_region_name: 17
source: dbSNP
start: 73411048
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1400219336
seq_region_name: 17
source: dbSNP
start: 73411057
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1029430429
seq_region_name: 17
source: dbSNP
start: 73411058
strand: 1
-
alleles:
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- TCCTTCCTCTGCCTCCCCCTCCTTCCTCTGCCTCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1443220183
seq_region_name: 17
source: dbSNP
start: 73411058
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599538538
seq_region_name: 17
source: dbSNP
start: 73411063
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1243610433
seq_region_name: 17
source: dbSNP
start: 73411064
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1346339868
seq_region_name: 17
source: dbSNP
start: 73411070
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs775010739
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs139686020
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411073
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411074
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs886540898
seq_region_name: 17
source: dbSNP
start: 73411075
strand: 1
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alleles:
- C
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411076
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411077
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411078
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411081
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411084
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs981458908
seq_region_name: 17
source: dbSNP
start: 73411087
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs188240559
seq_region_name: 17
source: dbSNP
start: 73411089
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411090
strand: 1
-
alleles:
- AGGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1357077394
seq_region_name: 17
source: dbSNP
start: 73411090
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1046540370
seq_region_name: 17
source: dbSNP
start: 73411092
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063122241
seq_region_name: 17
source: dbSNP
start: 73411093
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs906738520
seq_region_name: 17
source: dbSNP
start: 73411094
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411097
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411099
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs956359275
seq_region_name: 17
source: dbSNP
start: 73411102
strand: 1
-
alleles:
- CGGCAGCG
- CGGCAGCGGCAGCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411102
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs11650320
seq_region_name: 17
source: dbSNP
start: 73411103
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063122432
seq_region_name: 17
source: dbSNP
start: 73411104
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1307388576
seq_region_name: 17
source: dbSNP
start: 73411108
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411109
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs914756799
seq_region_name: 17
source: dbSNP
start: 73411111
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411113
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411117
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1476059898
seq_region_name: 17
source: dbSNP
start: 73411120
strand: 1
-
alleles:
- AATTCA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063122643
seq_region_name: 17
source: dbSNP
start: 73411121
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411124
feature_type: variation
id: rs566361275
seq_region_name: 17
source: dbSNP
start: 73411124
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411129
feature_type: variation
id: rs2063122702
seq_region_name: 17
source: dbSNP
start: 73411129
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411130
feature_type: variation
id: rs1217320631
seq_region_name: 17
source: dbSNP
start: 73411130
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs77373436
seq_region_name: 17
source: dbSNP
start: 73411134
strand: 1
-
alleles:
- CT
- CTTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411135
feature_type: variation
id: rs1449336402
seq_region_name: 17
source: dbSNP
start: 73411134
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411139
feature_type: variation
id: rs1050791392
seq_region_name: 17
source: dbSNP
start: 73411139
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411141
feature_type: variation
id: rs2063122823
seq_region_name: 17
source: dbSNP
start: 73411141
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411142
feature_type: variation
id: rs2063122851
seq_region_name: 17
source: dbSNP
start: 73411142
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411145
feature_type: variation
id: rs890877156
seq_region_name: 17
source: dbSNP
start: 73411145
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411148
feature_type: variation
id: rs1004403320
seq_region_name: 17
source: dbSNP
start: 73411148
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411155
feature_type: variation
id: rs1362575477
seq_region_name: 17
source: dbSNP
start: 73411155
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411158
feature_type: variation
id: rs554750106
seq_region_name: 17
source: dbSNP
start: 73411158
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411159
feature_type: variation
id: rs1021751061
seq_region_name: 17
source: dbSNP
start: 73411159
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411161
feature_type: variation
id: rs1326625971
seq_region_name: 17
source: dbSNP
start: 73411161
strand: 1
-
alleles:
- TTG
- TTGTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411165
feature_type: variation
id: rs1409102187
seq_region_name: 17
source: dbSNP
start: 73411163
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411166
feature_type: variation
id: rs2063123030
seq_region_name: 17
source: dbSNP
start: 73411166
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411171
feature_type: variation
id: rs367765923
seq_region_name: 17
source: dbSNP
start: 73411171
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411173
feature_type: variation
id: rs73999043
seq_region_name: 17
source: dbSNP
start: 73411173
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411176
feature_type: variation
id: rs969993817
seq_region_name: 17
source: dbSNP
start: 73411176
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411178
feature_type: variation
id: rs1002827499
seq_region_name: 17
source: dbSNP
start: 73411178
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411182
feature_type: variation
id: rs753850857
seq_region_name: 17
source: dbSNP
start: 73411182
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411184
feature_type: variation
id: rs2063123132
seq_region_name: 17
source: dbSNP
start: 73411184
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411186
feature_type: variation
id: rs2063123162
seq_region_name: 17
source: dbSNP
start: 73411186
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411191
feature_type: variation
id: rs2063123186
seq_region_name: 17
source: dbSNP
start: 73411191
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411192
feature_type: variation
id: rs755064583
seq_region_name: 17
source: dbSNP
start: 73411192
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411193
feature_type: variation
id: rs2063123232
seq_region_name: 17
source: dbSNP
start: 73411193
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411194
feature_type: variation
id: rs1168657819
seq_region_name: 17
source: dbSNP
start: 73411194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411201
feature_type: variation
id: rs2063123271
seq_region_name: 17
source: dbSNP
start: 73411201
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411202
feature_type: variation
id: rs2063123300
seq_region_name: 17
source: dbSNP
start: 73411202
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411203
feature_type: variation
id: rs777623589
seq_region_name: 17
source: dbSNP
start: 73411203
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411204
feature_type: variation
id: rs954502999
seq_region_name: 17
source: dbSNP
start: 73411204
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411216
feature_type: variation
id: rs1036136780
seq_region_name: 17
source: dbSNP
start: 73411216
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411229
feature_type: variation
id: rs2063123376
seq_region_name: 17
source: dbSNP
start: 73411229
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411234
feature_type: variation
id: rs1193711830
seq_region_name: 17
source: dbSNP
start: 73411234
strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411283
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73411290
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411293
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1304330557
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1443118276
seq_region_name: 17
source: dbSNP
start: 73411297
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1374962492
seq_region_name: 17
source: dbSNP
start: 73411298
strand: 1
-
alleles:
- CCCCC
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411313
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs968885852
seq_region_name: 17
source: dbSNP
start: 73411315
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145557873
seq_region_name: 17
source: dbSNP
start: 73411316
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs983294222
seq_region_name: 17
source: dbSNP
start: 73411317
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411322
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411323
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568388603
seq_region_name: 17
source: dbSNP
start: 73411330
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs11867668
seq_region_name: 17
source: dbSNP
start: 73411333
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs549872082
seq_region_name: 17
source: dbSNP
start: 73411334
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411335
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063124153
seq_region_name: 17
source: dbSNP
start: 73411336
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73411340
feature_type: variation
id: rs2145557923
seq_region_name: 17
source: dbSNP
start: 73411340
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs780831444
seq_region_name: 17
source: dbSNP
start: 73411341
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73411345
feature_type: variation
id: rs2047464
seq_region_name: 17
source: dbSNP
start: 73411345
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145557951
seq_region_name: 17
source: dbSNP
start: 73411349
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063124258
seq_region_name: 17
source: dbSNP
start: 73411351
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063124288
seq_region_name: 17
source: dbSNP
start: 73411354
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411356
feature_type: variation
id: rs2063124316
seq_region_name: 17
source: dbSNP
start: 73411356
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063124341
seq_region_name: 17
source: dbSNP
start: 73411359
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
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id: rs2063124364
seq_region_name: 17
source: dbSNP
start: 73411364
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1224853570
seq_region_name: 17
source: dbSNP
start: 73411366
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1480735117
seq_region_name: 17
source: dbSNP
start: 73411367
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411369
feature_type: variation
id: rs2063124431
seq_region_name: 17
source: dbSNP
start: 73411369
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063124450
seq_region_name: 17
source: dbSNP
start: 73411371
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411372
feature_type: variation
id: rs2063124474
seq_region_name: 17
source: dbSNP
start: 73411372
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411375
feature_type: variation
id: rs916602004
seq_region_name: 17
source: dbSNP
start: 73411375
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411376
feature_type: variation
id: rs2063124531
seq_region_name: 17
source: dbSNP
start: 73411376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411379
feature_type: variation
id: rs1234460555
seq_region_name: 17
source: dbSNP
start: 73411379
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411382
feature_type: variation
id: rs1208446271
seq_region_name: 17
source: dbSNP
start: 73411382
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411383
feature_type: variation
id: rs1568388635
seq_region_name: 17
source: dbSNP
start: 73411383
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411390
feature_type: variation
id: rs2063124634
seq_region_name: 17
source: dbSNP
start: 73411390
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411395
feature_type: variation
id: rs1599538907
seq_region_name: 17
source: dbSNP
start: 73411395
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411397
feature_type: variation
id: rs1485311032
seq_region_name: 17
source: dbSNP
start: 73411396
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411397
feature_type: variation
id: rs948316727
seq_region_name: 17
source: dbSNP
start: 73411397
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411400
feature_type: variation
id: rs2047465
seq_region_name: 17
source: dbSNP
start: 73411400
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411402
feature_type: variation
id: rs2063124787
seq_region_name: 17
source: dbSNP
start: 73411402
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411404
feature_type: variation
id: rs146213946
seq_region_name: 17
source: dbSNP
start: 73411404
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411405
feature_type: variation
id: rs574665914
seq_region_name: 17
source: dbSNP
start: 73411405
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411417
feature_type: variation
id: rs1052555145
seq_region_name: 17
source: dbSNP
start: 73411417
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411419
feature_type: variation
id: rs2145558104
seq_region_name: 17
source: dbSNP
start: 73411419
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411423
feature_type: variation
id: rs2145558115
seq_region_name: 17
source: dbSNP
start: 73411423
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411426
feature_type: variation
id: rs891543823
seq_region_name: 17
source: dbSNP
start: 73411426
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411427
feature_type: variation
id: rs1864494429
seq_region_name: 17
source: dbSNP
start: 73411427
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411429
feature_type: variation
id: rs2145558140
seq_region_name: 17
source: dbSNP
start: 73411429
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411431
feature_type: variation
id: rs898294677
seq_region_name: 17
source: dbSNP
start: 73411431
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411436
feature_type: variation
id: rs185512366
seq_region_name: 17
source: dbSNP
start: 73411436
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411437
feature_type: variation
id: rs1011777428
seq_region_name: 17
source: dbSNP
start: 73411437
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411442
feature_type: variation
id: rs1481857063
seq_region_name: 17
source: dbSNP
start: 73411442
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411445
feature_type: variation
id: rs1376622311
seq_region_name: 17
source: dbSNP
start: 73411444
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411446
feature_type: variation
id: rs2145558181
seq_region_name: 17
source: dbSNP
start: 73411446
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411448
feature_type: variation
id: rs1599538976
seq_region_name: 17
source: dbSNP
start: 73411448
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411455
feature_type: variation
id: rs2063125004
seq_region_name: 17
source: dbSNP
start: 73411455
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411456
feature_type: variation
id: rs1180442374
seq_region_name: 17
source: dbSNP
start: 73411456
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411457
feature_type: variation
id: rs557121086
seq_region_name: 17
source: dbSNP
start: 73411457
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411460
feature_type: variation
id: rs2145558216
seq_region_name: 17
source: dbSNP
start: 73411460
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411463
feature_type: variation
id: rs1361598513
seq_region_name: 17
source: dbSNP
start: 73411463
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411468
feature_type: variation
id: rs2145558234
seq_region_name: 17
source: dbSNP
start: 73411468
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411471
feature_type: variation
id: rs2063125103
seq_region_name: 17
source: dbSNP
start: 73411471
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411474
feature_type: variation
id: rs575314580
seq_region_name: 17
source: dbSNP
start: 73411474
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411475
feature_type: variation
id: rs1178702923
seq_region_name: 17
source: dbSNP
start: 73411475
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411476
feature_type: variation
id: rs545506778
seq_region_name: 17
source: dbSNP
start: 73411476
strand: 1
-
alleles:
- GCCTCCCCTCAAATGCTCTGCCTCCCCTC
- GCCTCCCCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411515
feature_type: variation
id: rs1427216496
seq_region_name: 17
source: dbSNP
start: 73411487
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411491
feature_type: variation
id: rs552814725
seq_region_name: 17
source: dbSNP
start: 73411491
strand: 1
-
alleles:
- CCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411494
feature_type: variation
id: rs1743735307
seq_region_name: 17
source: dbSNP
start: 73411491
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411496
feature_type: variation
id: rs2063125271
seq_region_name: 17
source: dbSNP
start: 73411496
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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-
alleles:
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-
alleles:
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alleles:
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-
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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- C
assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- GAA
assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73411682
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411683
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411684
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063126637
seq_region_name: 17
source: dbSNP
start: 73411685
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411687
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411689
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063126735
seq_region_name: 17
source: dbSNP
start: 73411696
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411702
strand: 1
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alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411706
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411707
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411709
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063126822
seq_region_name: 17
source: dbSNP
start: 73411710
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411712
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1193068469
seq_region_name: 17
source: dbSNP
start: 73411714
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063126879
seq_region_name: 17
source: dbSNP
start: 73411716
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1044197572
seq_region_name: 17
source: dbSNP
start: 73411721
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063126920
seq_region_name: 17
source: dbSNP
start: 73411729
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs570953097
seq_region_name: 17
source: dbSNP
start: 73411731
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145558732
seq_region_name: 17
source: dbSNP
start: 73411734
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411738
feature_type: variation
id: rs2063126965
seq_region_name: 17
source: dbSNP
start: 73411738
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063126983
seq_region_name: 17
source: dbSNP
start: 73411739
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1194470584
seq_region_name: 17
source: dbSNP
start: 73411740
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411741
feature_type: variation
id: rs1339086218
seq_region_name: 17
source: dbSNP
start: 73411741
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411742
feature_type: variation
id: rs1252232122
seq_region_name: 17
source: dbSNP
start: 73411742
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411743
feature_type: variation
id: rs1230310857
seq_region_name: 17
source: dbSNP
start: 73411743
strand: 1
-
alleles:
- GTTG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411747
feature_type: variation
id: rs2063127078
seq_region_name: 17
source: dbSNP
start: 73411744
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411746
feature_type: variation
id: rs938579888
seq_region_name: 17
source: dbSNP
start: 73411746
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411747
feature_type: variation
id: rs2063127122
seq_region_name: 17
source: dbSNP
start: 73411747
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063127379
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411789
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73411804
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73411805
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411806
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411813
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73411814
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs186892861
seq_region_name: 17
source: dbSNP
start: 73411815
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411816
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs556312602
seq_region_name: 17
source: dbSNP
start: 73411817
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1411356823
seq_region_name: 17
source: dbSNP
start: 73411818
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs900994982
seq_region_name: 17
source: dbSNP
start: 73411822
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411824
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73411824
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411827
feature_type: variation
id: rs2063128329
seq_region_name: 17
source: dbSNP
start: 73411827
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1188244061
seq_region_name: 17
source: dbSNP
start: 73411829
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411852
feature_type: variation
id: rs2145559114
seq_region_name: 17
source: dbSNP
start: 73411852
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145559121
seq_region_name: 17
source: dbSNP
start: 73411854
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1435234629
seq_region_name: 17
source: dbSNP
start: 73411855
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411857
feature_type: variation
id: rs1386076383
seq_region_name: 17
source: dbSNP
start: 73411857
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411858
feature_type: variation
id: rs568375627
seq_region_name: 17
source: dbSNP
start: 73411858
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145559154
seq_region_name: 17
source: dbSNP
start: 73411862
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411863
feature_type: variation
id: rs2063128451
seq_region_name: 17
source: dbSNP
start: 73411863
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063128475
seq_region_name: 17
source: dbSNP
start: 73411864
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs192232473
seq_region_name: 17
source: dbSNP
start: 73411866
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1364543044
seq_region_name: 17
source: dbSNP
start: 73411874
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411875
feature_type: variation
id: rs1389957641
seq_region_name: 17
source: dbSNP
start: 73411875
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1401169893
seq_region_name: 17
source: dbSNP
start: 73411886
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746562356
seq_region_name: 17
source: dbSNP
start: 73411888
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1669770061
seq_region_name: 17
source: dbSNP
start: 73411889
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599539494
seq_region_name: 17
source: dbSNP
start: 73411891
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411893
feature_type: variation
id: rs1212292412
seq_region_name: 17
source: dbSNP
start: 73411893
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1004835863
seq_region_name: 17
source: dbSNP
start: 73411896
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411897
feature_type: variation
id: rs1280195742
seq_region_name: 17
source: dbSNP
start: 73411897
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411905
feature_type: variation
id: rs1202791303
seq_region_name: 17
source: dbSNP
start: 73411905
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411906
feature_type: variation
id: rs1349506203
seq_region_name: 17
source: dbSNP
start: 73411906
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411909
feature_type: variation
id: rs1014746708
seq_region_name: 17
source: dbSNP
start: 73411909
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411913
feature_type: variation
id: rs2063128759
seq_region_name: 17
source: dbSNP
start: 73411913
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411914
feature_type: variation
id: rs2063128796
seq_region_name: 17
source: dbSNP
start: 73411914
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411919
feature_type: variation
id: rs1279728118
seq_region_name: 17
source: dbSNP
start: 73411919
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411920
feature_type: variation
id: rs575426365
seq_region_name: 17
source: dbSNP
start: 73411920
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411921
feature_type: variation
id: rs1353381376
seq_region_name: 17
source: dbSNP
start: 73411921
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411925
feature_type: variation
id: rs1292416217
seq_region_name: 17
source: dbSNP
start: 73411925
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411926
feature_type: variation
id: rs1415395711
seq_region_name: 17
source: dbSNP
start: 73411926
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411927
feature_type: variation
id: rs2063129004
seq_region_name: 17
source: dbSNP
start: 73411927
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411929
feature_type: variation
id: rs1201644867
seq_region_name: 17
source: dbSNP
start: 73411929
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411930
feature_type: variation
id: rs1316334361
seq_region_name: 17
source: dbSNP
start: 73411930
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411931
feature_type: variation
id: rs2063129128
seq_region_name: 17
source: dbSNP
start: 73411931
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411932
feature_type: variation
id: rs140943838
seq_region_name: 17
source: dbSNP
start: 73411932
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411943
feature_type: variation
id: rs763137302
seq_region_name: 17
source: dbSNP
start: 73411943
strand: 1
-
alleles:
- TGTGTGT
- TGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411949
feature_type: variation
id: rs2063129226
seq_region_name: 17
source: dbSNP
start: 73411943
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411944
feature_type: variation
id: rs1161586785
seq_region_name: 17
source: dbSNP
start: 73411944
strand: 1
-
alleles:
- TGTTTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411953
feature_type: variation
id: rs2063129293
seq_region_name: 17
source: dbSNP
start: 73411947
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411950
feature_type: variation
id: rs1460056524
seq_region_name: 17
source: dbSNP
start: 73411950
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411955
feature_type: variation
id: rs1837352501
seq_region_name: 17
source: dbSNP
start: 73411951
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411952
feature_type: variation
id: rs1417674268
seq_region_name: 17
source: dbSNP
start: 73411952
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411954
feature_type: variation
id: rs2063129424
seq_region_name: 17
source: dbSNP
start: 73411954
strand: 1
-
alleles:
- GTATATATATATATACGTATATATATAT
- GTATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411981
feature_type: variation
id: rs2063129457
seq_region_name: 17
source: dbSNP
start: 73411954
strand: 1
-
alleles:
- TATATATATATATA
- TATATATATATA
- TATATATATATATATA
- TATATATATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411968
feature_type: variation
id: rs546035555
seq_region_name: 17
source: dbSNP
start: 73411955
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411956
feature_type: variation
id: rs1029146059
seq_region_name: 17
source: dbSNP
start: 73411956
strand: 1
-
alleles:
- ATATATATATATA
- ATATATATATATATACGTATATATATATCTACATATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411968
feature_type: variation
id: rs2063129595
seq_region_name: 17
source: dbSNP
start: 73411956
strand: 1
-
alleles:
- ATATATATATATACGTATATATATATCTAC
- ATATATATATATACGTATATATATATCTACATATATATATATACGTATATATATATCTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs1491323214
seq_region_name: 17
source: dbSNP
start: 73411956
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411957
feature_type: variation
id: rs1445867156
seq_region_name: 17
source: dbSNP
start: 73411957
strand: 1
-
alleles:
- ATATATATATA
- ATATATATATATACGTATATATATATCTACATATATATATA
- ATATATATATATATACGTATATATATATCTACATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411968
feature_type: variation
id: rs1192206151
seq_region_name: 17
source: dbSNP
start: 73411958
strand: 1
-
alleles:
- ATATATATATACGTATATATATATCTAC
- ATATATATATACGTATATATATATCTACATATATATATACGTATATATATATCTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs1555764184
seq_region_name: 17
source: dbSNP
start: 73411958
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411959
feature_type: variation
id: rs1272381480
seq_region_name: 17
source: dbSNP
start: 73411959
strand: 1
-
alleles:
- TATATATATA
- TATATATATATACGTATATATATATCTACGTATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411968
feature_type: variation
id: rs1599539609
seq_region_name: 17
source: dbSNP
start: 73411959
strand: 1
-
alleles:
- TATATATATACGT
- TATATATATACGTGTATATATATCTACATATATATATACACGTATATATATATCTACGTATATATATACGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411971
feature_type: variation
id: rs2063129864
seq_region_name: 17
source: dbSNP
start: 73411959
strand: 1
-
alleles:
- TATATATATACGTA
- TATATATATACGTAGATATATATCTACGTATATATATACGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411972
feature_type: variation
id: rs1568388962
seq_region_name: 17
source: dbSNP
start: 73411959
strand: 1
-
alleles:
- TATATATATACGTATATATATATCTAC
- TATATATATACGTATATATATATCTACATATATATATATACGTAGATATATATCTACGTATATATATACGTATATATATATCTACGTATATATATACGTATATATATATCTAC
- TATATATATACGTATATATATATCTACATATATATATATACGTATATATATATCTACGTATATATATACGTATATATATATCTAC
- TATATATATACGTATATATATATCTACATATATATATATACGTATATATATATCTACGTATATATATACGTATATATATATCTACGTATATATATACGTATATATATATCTAC
- TATATATATACGTATATATATATCTACATATATATATCTACGTATATATATACGTATATATATATCTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs1568388965
seq_region_name: 17
source: dbSNP
start: 73411959
strand: 1
-
alleles:
- TATATATATACGTATATATATATCTACGTATATATATAC
- TATATATATAC
- TATATATATACGTATATATATATCTACGTATATATATACGTATATATATATCTACGTATATATATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411997
feature_type: variation
id: rs1372711822
seq_region_name: 17
source: dbSNP
start: 73411959
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411961
feature_type: variation
id: rs1224763948
seq_region_name: 17
source: dbSNP
start: 73411961
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411962
feature_type: variation
id: rs2063130107
seq_region_name: 17
source: dbSNP
start: 73411962
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411966
feature_type: variation
id: rs1430137037
seq_region_name: 17
source: dbSNP
start: 73411966
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411969
feature_type: variation
id: rs1286955516
seq_region_name: 17
source: dbSNP
start: 73411966
strand: 1
-
alleles:
- T
- TGTATATATATATCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411967
feature_type: variation
id: rs1463643233
seq_region_name: 17
source: dbSNP
start: 73411967
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411967
feature_type: variation
id: rs2063130227
seq_region_name: 17
source: dbSNP
start: 73411967
strand: 1
-
alleles:
- TACGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411972
feature_type: variation
id: rs1568388985
seq_region_name: 17
source: dbSNP
start: 73411967
strand: 1
-
alleles:
- TACGTATATATATATCTACGTATATAT
- TACGTATATATATATCTACGTATATATCTACGTATATATATATCTACGTATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411993
feature_type: variation
id: rs2063130340
seq_region_name: 17
source: dbSNP
start: 73411967
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411968
feature_type: variation
id: rs201638198
seq_region_name: 17
source: dbSNP
start: 73411968
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411969
feature_type: variation
id: rs66999713
seq_region_name: 17
source: dbSNP
start: 73411968
strand: 1
-
alleles:
- AC
- ACAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411969
feature_type: variation
id: rs771341219
seq_region_name: 17
source: dbSNP
start: 73411968
strand: 1
-
alleles:
- ACGTATATATATATCTACGTATATATATACAC
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411999
feature_type: variation
id: rs2063130520
seq_region_name: 17
source: dbSNP
start: 73411968
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411969
feature_type: variation
id: rs12937865
seq_region_name: 17
source: dbSNP
start: 73411969
strand: 1
-
alleles:
- CG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411970
feature_type: variation
id: rs1568388999
seq_region_name: 17
source: dbSNP
start: 73411969
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411970
feature_type: variation
id: rs144938031
seq_region_name: 17
source: dbSNP
start: 73411970
strand: 1
-
alleles:
- GTATATATATAT
- GTATATATATATATGTATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411981
feature_type: variation
id: rs2063130693
seq_region_name: 17
source: dbSNP
start: 73411970
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411971
feature_type: variation
id: rs2063130731
seq_region_name: 17
source: dbSNP
start: 73411971
strand: 1
-
alleles:
- TATATATATAT
- TATATATAT
- TATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411981
feature_type: variation
id: rs1244015937
seq_region_name: 17
source: dbSNP
start: 73411971
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411972
feature_type: variation
id: rs557473654
seq_region_name: 17
source: dbSNP
start: 73411972
strand: 1
-
alleles:
- A
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411972
feature_type: variation
id: rs2063130870
seq_region_name: 17
source: dbSNP
start: 73411972
strand: 1
-
alleles:
- ATATATATATCTAC
- ATATATATATCTACATATATATATACGAATATATATATCTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs2063130916
seq_region_name: 17
source: dbSNP
start: 73411972
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411973
feature_type: variation
id: rs1185169559
seq_region_name: 17
source: dbSNP
start: 73411973
strand: 1
-
alleles:
- TATATATATCTACGTATATATAT
- TATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411995
feature_type: variation
id: rs1418019107
seq_region_name: 17
source: dbSNP
start: 73411973
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411974
feature_type: variation
id: rs954876154
seq_region_name: 17
source: dbSNP
start: 73411974
strand: 1
-
alleles:
- ATATATATCTACGTATATATATAC
- ATATATATCTACGTATATATATACGTAGATATATATCTACGTATATATATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411997
feature_type: variation
id: rs2145559596
seq_region_name: 17
source: dbSNP
start: 73411974
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411975
feature_type: variation
id: rs1248179725
seq_region_name: 17
source: dbSNP
start: 73411975
strand: 1
-
alleles:
- TATATATCTACGTATATAT
- TATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411993
feature_type: variation
id: rs2063131066
seq_region_name: 17
source: dbSNP
start: 73411975
strand: 1
-
alleles:
- TATCTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411984
feature_type: variation
id: rs2063131093
seq_region_name: 17
source: dbSNP
start: 73411979
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411980
feature_type: variation
id: rs1189925503
seq_region_name: 17
source: dbSNP
start: 73411980
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411981
feature_type: variation
id: rs2063131193
seq_region_name: 17
source: dbSNP
start: 73411981
strand: 1
-
alleles:
- TCTACGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411987
feature_type: variation
id: rs2063131231
seq_region_name: 17
source: dbSNP
start: 73411981
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411982
feature_type: variation
id: rs1470473908
seq_region_name: 17
source: dbSNP
start: 73411982
strand: 1
-
alleles:
- CTAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs2063131310
seq_region_name: 17
source: dbSNP
start: 73411982
strand: 1
-
alleles:
- TAC
- TACATATATATATATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs2063131346
seq_region_name: 17
source: dbSNP
start: 73411983
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411984
feature_type: variation
id: rs1251919988
seq_region_name: 17
source: dbSNP
start: 73411984
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs1160294520
seq_region_name: 17
source: dbSNP
start: 73411984
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs572615729
seq_region_name: 17
source: dbSNP
start: 73411985
strand: 1
-
alleles:
- C
- CATATATATATATACGTATATATATATCTACGTATATATATACGTATATATATATCTCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs2063131501
seq_region_name: 17
source: dbSNP
start: 73411985
strand: 1
-
alleles:
- "-"
- AT
- ATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411985
feature_type: variation
id: rs1568389030
seq_region_name: 17
source: dbSNP
start: 73411986
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411986
feature_type: variation
id: rs200799695
seq_region_name: 17
source: dbSNP
start: 73411986
strand: 1
-
alleles:
- GT
- GTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411987
feature_type: variation
id: rs1568389031
seq_region_name: 17
source: dbSNP
start: 73411986
strand: 1
-
alleles:
- GT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411987
feature_type: variation
id: rs1568389034
seq_region_name: 17
source: dbSNP
start: 73411986
strand: 1
-
alleles:
- T
- TGTAT
- TGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411987
feature_type: variation
id: rs1555764210
seq_region_name: 17
source: dbSNP
start: 73411987
strand: 1
-
alleles:
- TAT
- TATCTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411989
feature_type: variation
id: rs2063131718
seq_region_name: 17
source: dbSNP
start: 73411987
strand: 1
-
alleles:
- TATATATATA
- TATATATA
- TATATATATATA
- TATATATATATATA
- TATATATATATATATA
- TATATATATATATATATA
- TATATATATATCTACGTATATATATACGTATATATATATCTACGTATATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411996
feature_type: variation
id: rs71157010
seq_region_name: 17
source: dbSNP
start: 73411987
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411988
feature_type: variation
id: rs1409634487
seq_region_name: 17
source: dbSNP
start: 73411988
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411989
feature_type: variation
id: rs2063131877
seq_region_name: 17
source: dbSNP
start: 73411989
strand: 1
-
alleles:
- ATATATACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411998
feature_type: variation
id: rs2063131910
seq_region_name: 17
source: dbSNP
start: 73411990
strand: 1
-
alleles:
- A
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411992
feature_type: variation
id: rs1568389050
seq_region_name: 17
source: dbSNP
start: 73411992
strand: 1
-
alleles:
- ATATACACACATATA
- ATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412006
feature_type: variation
id: rs1568389053
seq_region_name: 17
source: dbSNP
start: 73411992
strand: 1
-
alleles:
- A
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411994
feature_type: variation
id: rs1568389056
seq_region_name: 17
source: dbSNP
start: 73411994
strand: 1
-
alleles:
- ATACACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412000
feature_type: variation
id: rs2063132048
seq_region_name: 17
source: dbSNP
start: 73411994
strand: 1
-
alleles:
- ATACACACATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412004
feature_type: variation
id: rs1336770768
seq_region_name: 17
source: dbSNP
start: 73411994
strand: 1
-
alleles:
- T
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411995
feature_type: variation
id: rs1407872998
seq_region_name: 17
source: dbSNP
start: 73411995
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411995
feature_type: variation
id: rs2145559785
seq_region_name: 17
source: dbSNP
start: 73411995
strand: 1
-
alleles:
- A
- ATAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411996
feature_type: variation
id: rs1438714809
seq_region_name: 17
source: dbSNP
start: 73411996
strand: 1
-
alleles:
- ACACACA
- A
- ACA
- ACACA
- ACACACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412002
feature_type: variation
id: rs1383067681
seq_region_name: 17
source: dbSNP
start: 73411996
strand: 1
-
alleles:
- ACACACATATATATGTAGA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412014
feature_type: variation
id: rs1568389074
seq_region_name: 17
source: dbSNP
start: 73411996
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411996
feature_type: variation
id: rs2063132313
seq_region_name: 17
source: dbSNP
start: 73411997
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411997
feature_type: variation
id: rs12937898
seq_region_name: 17
source: dbSNP
start: 73411997
strand: 1
-
alleles:
- CACACAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412003
feature_type: variation
id: rs2063132411
seq_region_name: 17
source: dbSNP
start: 73411997
strand: 1
-
alleles:
- CACACATATATATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412010
feature_type: variation
id: rs2063132457
seq_region_name: 17
source: dbSNP
start: 73411997
strand: 1
-
alleles:
- CACACATATATATGTAGATATACGTATATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412026
feature_type: variation
id: rs1393877678
seq_region_name: 17
source: dbSNP
start: 73411997
strand: 1
-
alleles:
- "-"
- GTATATATATATCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411997
feature_type: variation
id: rs2063132533
seq_region_name: 17
source: dbSNP
start: 73411998
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411998
feature_type: variation
id: rs1326767357
seq_region_name: 17
source: dbSNP
start: 73411998
strand: 1
-
alleles:
- ACACATATATATGTAGATATAC
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412019
feature_type: variation
id: rs2063132621
seq_region_name: 17
source: dbSNP
start: 73411998
strand: 1
-
alleles:
- "-"
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411998
feature_type: variation
id: rs1568389086
seq_region_name: 17
source: dbSNP
start: 73411999
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411999
feature_type: variation
id: rs1438847164
seq_region_name: 17
source: dbSNP
start: 73411999
strand: 1
-
alleles:
- "-"
- GT
- GTATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73411999
feature_type: variation
id: rs1599539783
seq_region_name: 17
source: dbSNP
start: 73412000
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412000
feature_type: variation
id: rs1324203057
seq_region_name: 17
source: dbSNP
start: 73412000
strand: 1
-
alleles:
- ACATA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412004
feature_type: variation
id: rs2063132814
seq_region_name: 17
source: dbSNP
start: 73412000
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412001
feature_type: variation
id: rs889151777
seq_region_name: 17
source: dbSNP
start: 73412001
strand: 1
-
alleles:
- "-"
- GT
- GTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412001
feature_type: variation
id: rs1568389097
seq_region_name: 17
source: dbSNP
start: 73412002
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412002
feature_type: variation
id: rs1411074691
seq_region_name: 17
source: dbSNP
start: 73412002
strand: 1
-
alleles:
- ATATATAT
- ATAT
- ATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412009
feature_type: variation
id: rs1568389102
seq_region_name: 17
source: dbSNP
start: 73412002
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412003
feature_type: variation
id: rs12946665
seq_region_name: 17
source: dbSNP
start: 73412003
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412004
feature_type: variation
id: rs1169945442
seq_region_name: 17
source: dbSNP
start: 73412004
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412005
feature_type: variation
id: rs1568389107
seq_region_name: 17
source: dbSNP
start: 73412005
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412007
feature_type: variation
id: rs1451990778
seq_region_name: 17
source: dbSNP
start: 73412007
strand: 1
-
alleles:
- TATGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412012
feature_type: variation
id: rs1281827428
seq_region_name: 17
source: dbSNP
start: 73412007
strand: 1
-
alleles:
- TATGTAGATATACGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412023
feature_type: variation
id: rs1555764224
seq_region_name: 17
source: dbSNP
start: 73412007
strand: 1
-
alleles:
- AT
- ATCTACAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412009
feature_type: variation
id: rs2063133171
seq_region_name: 17
source: dbSNP
start: 73412008
strand: 1
-
alleles:
- ATGTAGAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412015
feature_type: variation
id: rs1327656570
seq_region_name: 17
source: dbSNP
start: 73412008
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412009
feature_type: variation
id: rs1394128242
seq_region_name: 17
source: dbSNP
start: 73412009
strand: 1
-
alleles:
- T
- TCTACGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412009
feature_type: variation
id: rs1945647954
seq_region_name: 17
source: dbSNP
start: 73412009
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412011
feature_type: variation
id: rs1227893976
seq_region_name: 17
source: dbSNP
start: 73412009
strand: 1
-
alleles:
- "-"
- CTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412009
feature_type: variation
id: rs1599539853
seq_region_name: 17
source: dbSNP
start: 73412010
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412010
feature_type: variation
id: rs1275122756
seq_region_name: 17
source: dbSNP
start: 73412010
strand: 1
-
alleles:
- GTAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412013
feature_type: variation
id: rs1191464789
seq_region_name: 17
source: dbSNP
start: 73412010
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412011
feature_type: variation
id: rs1231032759
seq_region_name: 17
source: dbSNP
start: 73412011
strand: 1
-
alleles:
- TA
- TATA
- TATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412012
feature_type: variation
id: rs528560397
seq_region_name: 17
source: dbSNP
start: 73412011
strand: 1
-
alleles:
- AGA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412014
feature_type: variation
id: rs2063133458
seq_region_name: 17
source: dbSNP
start: 73412012
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412013
feature_type: variation
id: rs1203479068
seq_region_name: 17
source: dbSNP
start: 73412013
strand: 1
-
alleles:
- GATATACG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412020
feature_type: variation
id: rs2063133521
seq_region_name: 17
source: dbSNP
start: 73412013
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412014
feature_type: variation
id: rs2063133550
seq_region_name: 17
source: dbSNP
start: 73412014
strand: 1
-
alleles:
- ATATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412018
feature_type: variation
id: rs1568389133
seq_region_name: 17
source: dbSNP
start: 73412014
strand: 1
-
alleles:
- ATATACGTATATGTATATATACGTATAT
- ATATACGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412041
feature_type: variation
id: rs71157011
seq_region_name: 17
source: dbSNP
start: 73412014
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412015
feature_type: variation
id: rs1232207559
seq_region_name: 17
source: dbSNP
start: 73412015
strand: 1
-
alleles:
- TATACGTATATGTATATATACGTATATATATGTATATACGTATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412058
feature_type: variation
id: rs1568389142
seq_region_name: 17
source: dbSNP
start: 73412015
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412016
feature_type: variation
id: rs1347306257
seq_region_name: 17
source: dbSNP
start: 73412016
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412019
feature_type: variation
id: rs1568389157
seq_region_name: 17
source: dbSNP
start: 73412016
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412017
feature_type: variation
id: rs1221220324
seq_region_name: 17
source: dbSNP
start: 73412017
strand: 1
-
alleles:
- TA
- TATATCTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412018
feature_type: variation
id: rs2063133847
seq_region_name: 17
source: dbSNP
start: 73412017
strand: 1
-
alleles:
- TACGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412022
feature_type: variation
id: rs1568389164
seq_region_name: 17
source: dbSNP
start: 73412017
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412018
feature_type: variation
id: rs561746976
seq_region_name: 17
source: dbSNP
start: 73412018
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412019
feature_type: variation
id: rs1568389165
seq_region_name: 17
source: dbSNP
start: 73412018
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412019
feature_type: variation
id: rs1279352429
seq_region_name: 17
source: dbSNP
start: 73412019
strand: 1
-
alleles:
- CG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412020
feature_type: variation
id: rs1263776096
seq_region_name: 17
source: dbSNP
start: 73412019
strand: 1
-
alleles:
- CGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412021
feature_type: variation
id: rs2063134083
seq_region_name: 17
source: dbSNP
start: 73412019
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412020
feature_type: variation
id: rs1372981633
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- GT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412021
feature_type: variation
id: rs1568389176
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- GTATAT
- GTATATATATGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412025
feature_type: variation
id: rs2063134221
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- GTATATGTATAT
- GTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412031
feature_type: variation
id: rs1568389177
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- GTATATGTATATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412033
feature_type: variation
id: rs1568389179
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- GTATATGTATATATACGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412037
feature_type: variation
id: rs1568389182
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- GTATATGTATATATACGTATATATATGTATATACGTATATGTATAT
- GTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412065
feature_type: variation
id: rs1443300959
seq_region_name: 17
source: dbSNP
start: 73412020
strand: 1
-
alleles:
- T
- TGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412021
feature_type: variation
id: rs2063134373
seq_region_name: 17
source: dbSNP
start: 73412021
strand: 1
-
alleles:
- TATAT
- T
- TATATAT
- TATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412025
feature_type: variation
id: rs1311543823
seq_region_name: 17
source: dbSNP
start: 73412021
strand: 1
-
alleles:
- TATATGTATATATA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412034
feature_type: variation
id: rs1568389187
seq_region_name: 17
source: dbSNP
start: 73412021
strand: 1
-
alleles:
- TATATGTATATATA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412034
feature_type: variation
id: rs1568389190
seq_region_name: 17
source: dbSNP
start: 73412021
strand: 1
-
alleles:
- TATATGTATATATACGTATATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412043
feature_type: variation
id: rs2063134566
seq_region_name: 17
source: dbSNP
start: 73412021
strand: 1
-
alleles:
- TATATGTATATATACGTATATATATGTATATACGTATATGTATATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412067
feature_type: variation
id: rs2063134600
seq_region_name: 17
source: dbSNP
start: 73412021
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412023
feature_type: variation
id: rs1434621150
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TAT
- TATATATATCTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412025
feature_type: variation
id: rs2063134679
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412029
feature_type: variation
id: rs1568389196
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TATGTATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412035
feature_type: variation
id: rs2063134748
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TATGTATATATACGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412039
feature_type: variation
id: rs2063134795
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TATGTATATATACGTATATATATGTATATACGTATATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412063
feature_type: variation
id: rs758511783
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TATGTATATATACGTATATATATGTATATACGTATATGTATATATACGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412073
feature_type: variation
id: rs1325943552
seq_region_name: 17
source: dbSNP
start: 73412023
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412027
feature_type: variation
id: rs879373427
seq_region_name: 17
source: dbSNP
start: 73412025
strand: 1
-
alleles:
- TGTATATATACGTATATATATGTATATACGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412055
feature_type: variation
id: rs1568389204
seq_region_name: 17
source: dbSNP
start: 73412025
strand: 1
-
alleles:
- TGTATATATACGTATATATATGTATATACGTATATGTATATATACGTATATATGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412079
feature_type: variation
id: rs2063134972
seq_region_name: 17
source: dbSNP
start: 73412025
strand: 1
-
alleles:
- "-"
- ATAC
- ATATATCTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412025
feature_type: variation
id: rs2063135010
seq_region_name: 17
source: dbSNP
start: 73412026
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412026
feature_type: variation
id: rs28566571
seq_region_name: 17
source: dbSNP
start: 73412026
strand: 1
-
alleles:
- TATATATA
- TATATA
- TATATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412034
feature_type: variation
id: rs2063135098
seq_region_name: 17
source: dbSNP
start: 73412027
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412028
feature_type: variation
id: rs1599540000
seq_region_name: 17
source: dbSNP
start: 73412028
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412029
feature_type: variation
id: rs376415036
seq_region_name: 17
source: dbSNP
start: 73412029
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412029
feature_type: variation
id: rs1176155356
seq_region_name: 17
source: dbSNP
start: 73412029
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412030
feature_type: variation
id: rs371254970
seq_region_name: 17
source: dbSNP
start: 73412030
strand: 1
-
alleles:
- ATATACGTATATATATGTATATACGTATATGTATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs1568389221
seq_region_name: 17
source: dbSNP
start: 73412030
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412031
feature_type: variation
id: rs1881079768
seq_region_name: 17
source: dbSNP
start: 73412031
strand: 1
-
alleles:
- TA
- TACGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412032
feature_type: variation
id: rs2063135336
seq_region_name: 17
source: dbSNP
start: 73412031
strand: 1
-
alleles:
- TAT
- TATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412033
feature_type: variation
id: rs1176437211
seq_region_name: 17
source: dbSNP
start: 73412031
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412032
feature_type: variation
id: rs1253675255
seq_region_name: 17
source: dbSNP
start: 73412032
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412035
feature_type: variation
id: rs2063135446
seq_region_name: 17
source: dbSNP
start: 73412032
strand: 1
-
alleles:
- ATACGTATATATATGTATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs2063135470
seq_region_name: 17
source: dbSNP
start: 73412032
strand: 1
-
alleles:
- ATACGTATATATATGTATATACGTATATGTATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs879470887
seq_region_name: 17
source: dbSNP
start: 73412032
strand: 1
-
alleles:
- ATACGTATATATATGTATATACGTATATGTATATATACGTATATATGTATATGTATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412093
feature_type: variation
id: rs2063135526
seq_region_name: 17
source: dbSNP
start: 73412032
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412033
feature_type: variation
id: rs1568389234
seq_region_name: 17
source: dbSNP
start: 73412033
strand: 1
-
alleles:
- TACGTATATATATGTATATACGTATATGTATATATACGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412072
feature_type: variation
id: rs1568389241
seq_region_name: 17
source: dbSNP
start: 73412033
strand: 1
-
alleles:
- "-"
- GTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412033
feature_type: variation
id: rs2063135601
seq_region_name: 17
source: dbSNP
start: 73412034
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412034
feature_type: variation
id: rs1485301286
seq_region_name: 17
source: dbSNP
start: 73412034
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412035
feature_type: variation
id: rs1568389245
seq_region_name: 17
source: dbSNP
start: 73412034
strand: 1
-
alleles:
- ACGTATATATATGTATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs2063135666
seq_region_name: 17
source: dbSNP
start: 73412034
strand: 1
-
alleles:
- ACGTATATATATGTATATACGTATATGTATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs1568389248
seq_region_name: 17
source: dbSNP
start: 73412034
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412035
feature_type: variation
id: rs1212260364
seq_region_name: 17
source: dbSNP
start: 73412035
strand: 1
-
alleles:
- CG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412036
feature_type: variation
id: rs1255729864
seq_region_name: 17
source: dbSNP
start: 73412035
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412036
feature_type: variation
id: rs756839710
seq_region_name: 17
source: dbSNP
start: 73412036
strand: 1
-
alleles:
- GT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412037
feature_type: variation
id: rs1568389259
seq_region_name: 17
source: dbSNP
start: 73412036
strand: 1
-
alleles:
- GTATATATATGTATATACGTATATGTATAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412065
feature_type: variation
id: rs2063135830
seq_region_name: 17
source: dbSNP
start: 73412036
strand: 1
-
alleles:
- GTATATATATGTATATACGTATATGTATATATA
- GTATATATATGTATATACGTATATGTATATATATGTATATACGTATATGTATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412068
feature_type: variation
id: rs1568389257
seq_region_name: 17
source: dbSNP
start: 73412036
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412037
feature_type: variation
id: rs373807517
seq_region_name: 17
source: dbSNP
start: 73412037
strand: 1
-
alleles:
- T
- TTTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412037
feature_type: variation
id: rs2063135910
seq_region_name: 17
source: dbSNP
start: 73412037
strand: 1
-
alleles:
- TATATATAT
- TATATAT
- TATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412045
feature_type: variation
id: rs1306513151
seq_region_name: 17
source: dbSNP
start: 73412037
strand: 1
-
alleles:
- A
- ACACA
- ACACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412038
feature_type: variation
id: rs1568389265
seq_region_name: 17
source: dbSNP
start: 73412038
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412038
feature_type: variation
id: rs2063135964
seq_region_name: 17
source: dbSNP
start: 73412038
strand: 1
-
alleles:
- ATATATAT
- ATATATATACACACATATATAT
- ATATATATATACACACATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412045
feature_type: variation
id: rs1568389270
seq_region_name: 17
source: dbSNP
start: 73412038
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412039
feature_type: variation
id: rs1352770349
seq_region_name: 17
source: dbSNP
start: 73412039
strand: 1
-
alleles:
- TAT
- TATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412041
feature_type: variation
id: rs1869516155
seq_region_name: 17
source: dbSNP
start: 73412039
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412040
feature_type: variation
id: rs367660268
seq_region_name: 17
source: dbSNP
start: 73412040
strand: 1
-
alleles:
- ATATAT
- ATATATACACATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412045
feature_type: variation
id: rs2063136105
seq_region_name: 17
source: dbSNP
start: 73412040
strand: 1
-
alleles:
- "-"
- CG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412040
feature_type: variation
id: rs1291790568
seq_region_name: 17
source: dbSNP
start: 73412041
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412041
feature_type: variation
id: rs1555764277
seq_region_name: 17
source: dbSNP
start: 73412041
strand: 1
-
alleles:
- TAT
- TATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412043
feature_type: variation
id: rs1555764278
seq_region_name: 17
source: dbSNP
start: 73412041
strand: 1
-
alleles:
- TATATGTATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412051
feature_type: variation
id: rs2063136196
seq_region_name: 17
source: dbSNP
start: 73412041
strand: 1
-
alleles:
- TATATGTATATACGTATATGTATATA
- TATATGTATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412066
feature_type: variation
id: rs2063136215
seq_region_name: 17
source: dbSNP
start: 73412041
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412042
feature_type: variation
id: rs1467092750
seq_region_name: 17
source: dbSNP
start: 73412042
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412043
feature_type: variation
id: rs1343092389
seq_region_name: 17
source: dbSNP
start: 73412043
strand: 1
-
alleles:
- TATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412049
feature_type: variation
id: rs2063136286
seq_region_name: 17
source: dbSNP
start: 73412043
strand: 1
-
alleles:
- TATGTATATACGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412057
feature_type: variation
id: rs2063136313
seq_region_name: 17
source: dbSNP
start: 73412043
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412044
feature_type: variation
id: rs28580889
seq_region_name: 17
source: dbSNP
start: 73412044
strand: 1
-
alleles:
- ATGTATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs1568389288
seq_region_name: 17
source: dbSNP
start: 73412044
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412045
feature_type: variation
id: rs1413994658
seq_region_name: 17
source: dbSNP
start: 73412045
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412045
feature_type: variation
id: rs2063136410
seq_region_name: 17
source: dbSNP
start: 73412045
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412047
feature_type: variation
id: rs1457412665
seq_region_name: 17
source: dbSNP
start: 73412045
strand: 1
-
alleles:
- "-"
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412045
feature_type: variation
id: rs2063136491
seq_region_name: 17
source: dbSNP
start: 73412046
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412046
feature_type: variation
id: rs1445403549
seq_region_name: 17
source: dbSNP
start: 73412046
strand: 1
-
alleles:
- GTATATACGTATATGTATATATACGTATATA
- GTATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412076
feature_type: variation
id: rs1568389298
seq_region_name: 17
source: dbSNP
start: 73412046
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412047
feature_type: variation
id: rs2063136612
seq_region_name: 17
source: dbSNP
start: 73412047
strand: 1
-
alleles:
- TATATACGTATAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412059
feature_type: variation
id: rs2063136651
seq_region_name: 17
source: dbSNP
start: 73412047
strand: 1
-
alleles:
- TATATACGTATATGTATATATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412068
feature_type: variation
id: rs2063136686
seq_region_name: 17
source: dbSNP
start: 73412047
strand: 1
-
alleles:
- A
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412048
feature_type: variation
id: rs1249569937
seq_region_name: 17
source: dbSNP
start: 73412048
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412048
feature_type: variation
id: rs1474847639
seq_region_name: 17
source: dbSNP
start: 73412048
strand: 1
-
alleles:
- ATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs2063136785
seq_region_name: 17
source: dbSNP
start: 73412048
strand: 1
-
alleles:
- ATATACGTATATGTATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs2063136815
seq_region_name: 17
source: dbSNP
start: 73412048
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412049
feature_type: variation
id: rs371794147
seq_region_name: 17
source: dbSNP
start: 73412049
strand: 1
-
alleles:
- TATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs1568389305
seq_region_name: 17
source: dbSNP
start: 73412049
strand: 1
-
alleles:
- TATACGTATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412058
feature_type: variation
id: rs1568389311
seq_region_name: 17
source: dbSNP
start: 73412049
strand: 1
-
alleles:
- TATACGTATATGTATATATACGTATATATGTATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412082
feature_type: variation
id: rs2063136978
seq_region_name: 17
source: dbSNP
start: 73412049
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412050
feature_type: variation
id: rs1484910184
seq_region_name: 17
source: dbSNP
start: 73412050
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs2063137062
seq_region_name: 17
source: dbSNP
start: 73412050
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412051
feature_type: variation
id: rs1209646154
seq_region_name: 17
source: dbSNP
start: 73412051
strand: 1
-
alleles:
- T
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412051
feature_type: variation
id: rs1568389318
seq_region_name: 17
source: dbSNP
start: 73412051
strand: 1
-
alleles:
- TACGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412056
feature_type: variation
id: rs373095116
seq_region_name: 17
source: dbSNP
start: 73412051
strand: 1
-
alleles:
- TACGTATATGTATATATACGTATATATGTATATGTATATATACGTATATATGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412104
feature_type: variation
id: rs2063137217
seq_region_name: 17
source: dbSNP
start: 73412051
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412052
feature_type: variation
id: rs1331463132
seq_region_name: 17
source: dbSNP
start: 73412052
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs2063137293
seq_region_name: 17
source: dbSNP
start: 73412052
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs71383049
seq_region_name: 17
source: dbSNP
start: 73412053
strand: 1
-
alleles:
- CG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412054
feature_type: variation
id: rs2063137390
seq_region_name: 17
source: dbSNP
start: 73412053
strand: 1
-
alleles:
- "-"
- ACAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412053
feature_type: variation
id: rs2063137424
seq_region_name: 17
source: dbSNP
start: 73412054
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412054
feature_type: variation
id: rs1322880037
seq_region_name: 17
source: dbSNP
start: 73412054
strand: 1
-
alleles:
- GTATATGTATATATACGTATATATGTATATGTATATATACGTATATATGTATA
- GTATATGTATATATACGTATATATGTATA
- GTATATGTATATATACGTATATATGTATATGTATATATACGTATATATGTATATGTATATATACGTATATATGTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412106
feature_type: variation
id: rs869089456
seq_region_name: 17
source: dbSNP
start: 73412054
strand: 1
-
alleles:
- TATAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412059
feature_type: variation
id: rs1315394039
seq_region_name: 17
source: dbSNP
start: 73412055
strand: 1
-
alleles:
- TATATGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412061
feature_type: variation
id: rs2063137648
seq_region_name: 17
source: dbSNP
start: 73412055
strand: 1
-
alleles:
- TATATGTAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412063
feature_type: variation
id: rs1472196650
seq_region_name: 17
source: dbSNP
start: 73412055
strand: 1
-
alleles:
- TATATGTATATATACGTATATATGTATAT
- TATATGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412083
feature_type: variation
id: rs2063137722
seq_region_name: 17
source: dbSNP
start: 73412055
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412056
feature_type: variation
id: rs1380994577
seq_region_name: 17
source: dbSNP
start: 73412056
strand: 1
-
alleles:
- TATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412063
feature_type: variation
id: rs1176543535
seq_region_name: 17
source: dbSNP
start: 73412057
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412058
feature_type: variation
id: rs1287769563
seq_region_name: 17
source: dbSNP
start: 73412058
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs374837530
seq_region_name: 17
source: dbSNP
start: 73412059
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412061
feature_type: variation
id: rs1491415870
seq_region_name: 17
source: dbSNP
start: 73412059
strand: 1
-
alleles:
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- ATAC
- CTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412059
feature_type: variation
id: rs2063137975
seq_region_name: 17
source: dbSNP
start: 73412060
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412060
feature_type: variation
id: rs1460684488
seq_region_name: 17
source: dbSNP
start: 73412060
strand: 1
-
alleles:
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- GTAGATATACGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412062
feature_type: variation
id: rs1491111740
seq_region_name: 17
source: dbSNP
start: 73412060
strand: 1
-
alleles:
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- GTATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412077
feature_type: variation
id: rs2063138081
seq_region_name: 17
source: dbSNP
start: 73412060
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412061
feature_type: variation
id: rs2063138119
seq_region_name: 17
source: dbSNP
start: 73412061
strand: 1
-
alleles:
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- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412068
feature_type: variation
id: rs1568389353
seq_region_name: 17
source: dbSNP
start: 73412061
strand: 1
-
alleles:
- TATATATACGTATATATGTATATGTATATATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412092
feature_type: variation
id: rs2063138191
seq_region_name: 17
source: dbSNP
start: 73412061
strand: 1
-
alleles:
- TATATATACGTATATATGTATATGTATATATACGTATATATGTATACGTATATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412115
feature_type: variation
id: rs2063138230
seq_region_name: 17
source: dbSNP
start: 73412061
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412062
feature_type: variation
id: rs1166877224
seq_region_name: 17
source: dbSNP
start: 73412062
strand: 1
-
alleles:
- ATA
- ATACACACATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412064
feature_type: variation
id: rs2063138310
seq_region_name: 17
source: dbSNP
start: 73412062
strand: 1
-
alleles:
- ATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs748943952
seq_region_name: 17
source: dbSNP
start: 73412062
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412063
feature_type: variation
id: rs796894279
seq_region_name: 17
source: dbSNP
start: 73412063
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412064
feature_type: variation
id: rs12939231
seq_region_name: 17
source: dbSNP
start: 73412064
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412065
feature_type: variation
id: rs1189288055
seq_region_name: 17
source: dbSNP
start: 73412065
strand: 1
-
alleles:
- T
- TGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412065
feature_type: variation
id: rs1882943897
seq_region_name: 17
source: dbSNP
start: 73412065
strand: 1
-
alleles:
- TAT
- TATGTGTATGTGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412067
feature_type: variation
id: rs2063138457
seq_region_name: 17
source: dbSNP
start: 73412065
strand: 1
-
alleles:
- TATACGTATATATGTATATGTATATATACGTATATATGTATACGTATATATGTATA
- TATACGTATATATGTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412120
feature_type: variation
id: rs1410914935
seq_region_name: 17
source: dbSNP
start: 73412065
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412066
feature_type: variation
id: rs2063138534
seq_region_name: 17
source: dbSNP
start: 73412066
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs1310190549
seq_region_name: 17
source: dbSNP
start: 73412066
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412067
feature_type: variation
id: rs1466423021
seq_region_name: 17
source: dbSNP
start: 73412067
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412068
feature_type: variation
id: rs1213496362
seq_region_name: 17
source: dbSNP
start: 73412068
strand: 1
-
alleles:
- A
- ATACA
- ATACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412068
feature_type: variation
id: rs1568389373
seq_region_name: 17
source: dbSNP
start: 73412068
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs752178698
seq_region_name: 17
source: dbSNP
start: 73412068
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412069
feature_type: variation
id: rs113135345
seq_region_name: 17
source: dbSNP
start: 73412069
strand: 1
-
alleles:
- CGTATATATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412078
feature_type: variation
id: rs2063138798
seq_region_name: 17
source: dbSNP
start: 73412069
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412070
feature_type: variation
id: rs1267585629
seq_region_name: 17
source: dbSNP
start: 73412070
strand: 1
-
alleles:
- GTAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412073
feature_type: variation
id: rs2063138865
seq_region_name: 17
source: dbSNP
start: 73412070
strand: 1
-
alleles:
- GTATATAT
- GTATATATATGTATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412077
feature_type: variation
id: rs2063138903
seq_region_name: 17
source: dbSNP
start: 73412070
strand: 1
-
alleles:
- TATATAT
- T
- TATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412077
feature_type: variation
id: rs1225953429
seq_region_name: 17
source: dbSNP
start: 73412071
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412072
feature_type: variation
id: rs745320520
seq_region_name: 17
source: dbSNP
start: 73412072
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412072
feature_type: variation
id: rs1409689796
seq_region_name: 17
source: dbSNP
start: 73412072
strand: 1
-
alleles:
- A
- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412072
feature_type: variation
id: rs2063139036
seq_region_name: 17
source: dbSNP
start: 73412072
strand: 1
-
alleles:
- TATATGT
- TATATGTGTATATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412079
feature_type: variation
id: rs2063139111
seq_region_name: 17
source: dbSNP
start: 73412073
strand: 1
-
alleles:
- TATATGTATATGTATAT
- TATATGTATATGTATATGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412089
feature_type: variation
id: rs2063139159
seq_region_name: 17
source: dbSNP
start: 73412073
strand: 1
-
alleles:
- ATATGTATATGTATATATACGTATATATGTATACGTA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412110
feature_type: variation
id: rs1347538556
seq_region_name: 17
source: dbSNP
start: 73412074
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412075
feature_type: variation
id: rs1228418971
seq_region_name: 17
source: dbSNP
start: 73412075
strand: 1
-
alleles:
- TATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412081
feature_type: variation
id: rs796630040
seq_region_name: 17
source: dbSNP
start: 73412075
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412076
feature_type: variation
id: rs1323428450
seq_region_name: 17
source: dbSNP
start: 73412076
strand: 1
-
alleles:
- T
- TATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412077
feature_type: variation
id: rs1366943504
seq_region_name: 17
source: dbSNP
start: 73412077
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412077
feature_type: variation
id: rs1385845490
seq_region_name: 17
source: dbSNP
start: 73412077
strand: 1
-
alleles:
- TGT
- T
- TGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412079
feature_type: variation
id: rs1491225083
seq_region_name: 17
source: dbSNP
start: 73412077
strand: 1
-
alleles:
- "-"
- ATGTATATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412077
feature_type: variation
id: rs1491395356
seq_region_name: 17
source: dbSNP
start: 73412078
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412078
feature_type: variation
id: rs1295054003
seq_region_name: 17
source: dbSNP
start: 73412078
strand: 1
-
alleles:
- GTA
- GTAGATATACGTA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412080
feature_type: variation
id: rs2063139547
seq_region_name: 17
source: dbSNP
start: 73412078
strand: 1
-
alleles:
- GTATAT
- GTATATACGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412083
feature_type: variation
id: rs2063139590
seq_region_name: 17
source: dbSNP
start: 73412078
strand: 1
-
alleles:
- TA
- TAGATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412080
feature_type: variation
id: rs1460460000
seq_region_name: 17
source: dbSNP
start: 73412079
strand: 1
-
alleles:
- TATAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412083
feature_type: variation
id: rs2063139682
seq_region_name: 17
source: dbSNP
start: 73412079
strand: 1
-
alleles:
- TATATGTATATATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412092
feature_type: variation
id: rs1197362750
seq_region_name: 17
source: dbSNP
start: 73412079
strand: 1
-
alleles:
- TATATGTATATATACGTATATAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412101
feature_type: variation
id: rs2063139761
seq_region_name: 17
source: dbSNP
start: 73412079
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412080
feature_type: variation
id: rs12939244
seq_region_name: 17
source: dbSNP
start: 73412080
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412081
feature_type: variation
id: rs2063139849
seq_region_name: 17
source: dbSNP
start: 73412081
strand: 1
-
alleles:
- TAT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412083
feature_type: variation
id: rs2063139895
seq_region_name: 17
source: dbSNP
start: 73412081
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412083
feature_type: variation
id: rs367910760
seq_region_name: 17
source: dbSNP
start: 73412083
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412085
feature_type: variation
id: rs1169332683
seq_region_name: 17
source: dbSNP
start: 73412083
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412084
feature_type: variation
id: rs1393317564
seq_region_name: 17
source: dbSNP
start: 73412084
strand: 1
-
alleles:
- GTATATA
- GTATATACGTATATGTATATATACGTATATATGTATACGTATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412090
feature_type: variation
id: rs2063140062
seq_region_name: 17
source: dbSNP
start: 73412084
strand: 1
-
alleles:
- GTATATATACGTATATATGTATA
- GTATATATACGTATATATGTATATGTATATATACGTATATATGTATACGTATATATACGTATATATGTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412106
feature_type: variation
id: rs2063140098
seq_region_name: 17
source: dbSNP
start: 73412084
strand: 1
-
alleles:
- GTATATATACGTATATATGTATACGTATATAT
- GTATATATACGTATATATGTATACGTATATATACGTATATATGTATACGTATATAT
- GTATATATACGTATATATGTATACGTATATATACGTATATATGTATACGTATATATACGTATATATGTATACGTATATAT
- GTATATATACGTATATATGTATACGTATATATACGTATATATGTATACGTATATATGTATACGTATATATACGTATATATGTATACGTATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412115
feature_type: variation
id: rs1568389420
seq_region_name: 17
source: dbSNP
start: 73412084
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412085
feature_type: variation
id: rs2063140164
seq_region_name: 17
source: dbSNP
start: 73412085
strand: 1
-
alleles:
- TATATATA
- TATA
- TATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412092
feature_type: variation
id: rs2063140189
seq_region_name: 17
source: dbSNP
start: 73412085
strand: 1
-
alleles:
- TATATATACGTATATAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412101
feature_type: variation
id: rs2063140228
seq_region_name: 17
source: dbSNP
start: 73412085
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412086
feature_type: variation
id: rs12939247
seq_region_name: 17
source: dbSNP
start: 73412086
strand: 1
-
alleles:
- ATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412093
feature_type: variation
id: rs753584566
seq_region_name: 17
source: dbSNP
start: 73412086
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412087
feature_type: variation
id: rs1452395092
seq_region_name: 17
source: dbSNP
start: 73412087
strand: 1
-
alleles:
- TATATACGTATATA
- TATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412100
feature_type: variation
id: rs1568389432
seq_region_name: 17
source: dbSNP
start: 73412087
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412088
feature_type: variation
id: rs1270002544
seq_region_name: 17
source: dbSNP
start: 73412088
strand: 1
-
alleles:
- ATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412093
feature_type: variation
id: rs2145561372
seq_region_name: 17
source: dbSNP
start: 73412088
strand: 1
-
alleles:
- ATATACGTATATATGTATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412107
feature_type: variation
id: rs2145561378
seq_region_name: 17
source: dbSNP
start: 73412088
strand: 1
-
alleles:
- TATACGTATATATGTATACGTATATATGTATACGTATATATGT
- TATACGTATATATGT
- TATACGTATATATGTATACGTATATATGT
- TATACGTATATATGTATACGTATATATGTATACGTATATATGTATACGTATATATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412131
feature_type: variation
id: rs796480464
seq_region_name: 17
source: dbSNP
start: 73412089
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412090
feature_type: variation
id: rs2063140391
seq_region_name: 17
source: dbSNP
start: 73412090
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412093
feature_type: variation
id: rs2063140411
seq_region_name: 17
source: dbSNP
start: 73412090
strand: 1
-
alleles:
- TACGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412096
feature_type: variation
id: rs2063140434
seq_region_name: 17
source: dbSNP
start: 73412091
strand: 1
-
alleles:
- TACGTATATATGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412104
feature_type: variation
id: rs2063140450
seq_region_name: 17
source: dbSNP
start: 73412091
strand: 1
-
alleles:
- TACGTATATATGTATACGTATATATGTATACGTATATATGTGTATGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412137
feature_type: variation
id: rs2063140479
seq_region_name: 17
source: dbSNP
start: 73412091
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412092
feature_type: variation
id: rs1275913032
seq_region_name: 17
source: dbSNP
start: 73412092
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412093
feature_type: variation
id: rs372046186
seq_region_name: 17
source: dbSNP
start: 73412092
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412093
feature_type: variation
id: rs1270948412
seq_region_name: 17
source: dbSNP
start: 73412093
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412094
feature_type: variation
id: rs2063140572
seq_region_name: 17
source: dbSNP
start: 73412093
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412094
feature_type: variation
id: rs1343728396
seq_region_name: 17
source: dbSNP
start: 73412094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063140607
seq_region_name: 17
source: dbSNP
start: 73412094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412101
feature_type: variation
id: rs1300596099
seq_region_name: 17
source: dbSNP
start: 73412095
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412096
feature_type: variation
id: rs375161886
seq_region_name: 17
source: dbSNP
start: 73412096
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412096
feature_type: variation
id: rs779286708
seq_region_name: 17
source: dbSNP
start: 73412096
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412106
feature_type: variation
id: rs1303135348
seq_region_name: 17
source: dbSNP
start: 73412097
strand: 1
-
alleles:
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- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412135
feature_type: variation
id: rs2063140749
seq_region_name: 17
source: dbSNP
start: 73412097
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412098
feature_type: variation
id: rs1369914030
seq_region_name: 17
source: dbSNP
start: 73412098
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412098
feature_type: variation
id: rs2063140795
seq_region_name: 17
source: dbSNP
start: 73412098
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412110
feature_type: variation
id: rs758925924
seq_region_name: 17
source: dbSNP
start: 73412098
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412099
feature_type: variation
id: rs1555764343
seq_region_name: 17
source: dbSNP
start: 73412099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412099
feature_type: variation
id: rs2063140849
seq_region_name: 17
source: dbSNP
start: 73412099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412101
feature_type: variation
id: rs1568389483
seq_region_name: 17
source: dbSNP
start: 73412099
strand: 1
-
alleles:
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- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412105
feature_type: variation
id: rs1308604123
seq_region_name: 17
source: dbSNP
start: 73412099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412100
feature_type: variation
id: rs12939492
seq_region_name: 17
source: dbSNP
start: 73412100
strand: 1
-
alleles:
- ATGTATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412107
feature_type: variation
id: rs777227657
seq_region_name: 17
source: dbSNP
start: 73412100
strand: 1
-
alleles:
- ATGTATACGTA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412110
feature_type: variation
id: rs2063140985
seq_region_name: 17
source: dbSNP
start: 73412100
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412101
feature_type: variation
id: rs2063141011
seq_region_name: 17
source: dbSNP
start: 73412101
strand: 1
-
alleles:
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- T
- TGTGTATGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412103
feature_type: variation
id: rs1431530075
seq_region_name: 17
source: dbSNP
start: 73412101
strand: 1
-
alleles:
- "-"
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412101
feature_type: variation
id: rs2063141059
seq_region_name: 17
source: dbSNP
start: 73412102
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412102
feature_type: variation
id: rs865962716
seq_region_name: 17
source: dbSNP
start: 73412102
strand: 1
-
alleles:
- GTATACGTATA
- GTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412112
feature_type: variation
id: rs1173087549
seq_region_name: 17
source: dbSNP
start: 73412102
strand: 1
-
alleles:
- GTATACGTATATATGTATACGTATA
- GTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412126
feature_type: variation
id: rs2063141129
seq_region_name: 17
source: dbSNP
start: 73412102
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412103
feature_type: variation
id: rs2063141148
seq_region_name: 17
source: dbSNP
start: 73412103
strand: 1
-
alleles:
- TATA
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- TATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412106
feature_type: variation
id: rs1568389505
seq_region_name: 17
source: dbSNP
start: 73412103
strand: 1
-
alleles:
- TATACGTATATAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412115
feature_type: variation
id: rs1379530643
seq_region_name: 17
source: dbSNP
start: 73412103
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412104
feature_type: variation
id: rs1310948490
seq_region_name: 17
source: dbSNP
start: 73412104
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412104
feature_type: variation
id: rs1568389512
seq_region_name: 17
source: dbSNP
start: 73412104
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412107
feature_type: variation
id: rs1568389514
seq_region_name: 17
source: dbSNP
start: 73412104
strand: 1
-
alleles:
- TACGTATATATGTATACGTATATATGTGTATGTGTATATGTATATATACGTATATATGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412164
feature_type: variation
id: rs1568389517
seq_region_name: 17
source: dbSNP
start: 73412105
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412107
feature_type: variation
id: rs375056594
seq_region_name: 17
source: dbSNP
start: 73412107
strand: 1
-
alleles:
- CGTATATATGTATACGTATATATGTGTATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412136
feature_type: variation
id: rs2145561660
seq_region_name: 17
source: dbSNP
start: 73412107
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412108
feature_type: variation
id: rs1252951266
seq_region_name: 17
source: dbSNP
start: 73412108
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412109
feature_type: variation
id: rs2063141348
seq_region_name: 17
source: dbSNP
start: 73412109
strand: 1
-
alleles:
- TATATAT
- TAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412115
feature_type: variation
id: rs1568389532
seq_region_name: 17
source: dbSNP
start: 73412109
strand: 1
-
alleles:
- TATATATGTATACGTATATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412129
feature_type: variation
id: rs2063141395
seq_region_name: 17
source: dbSNP
start: 73412109
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412110
feature_type: variation
id: rs62072148
seq_region_name: 17
source: dbSNP
start: 73412110
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412112
feature_type: variation
id: rs2063141459
seq_region_name: 17
source: dbSNP
start: 73412112
strand: 1
-
alleles:
- ATATGTATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412121
feature_type: variation
id: rs2063141484
seq_region_name: 17
source: dbSNP
start: 73412112
strand: 1
-
alleles:
- TATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412119
feature_type: variation
id: rs1327262697
seq_region_name: 17
source: dbSNP
start: 73412113
strand: 1
-
alleles:
- TATGTATACGTATATATGTGTATGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412137
feature_type: variation
id: rs2063141532
seq_region_name: 17
source: dbSNP
start: 73412113
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412114
feature_type: variation
id: rs1345292627
seq_region_name: 17
source: dbSNP
start: 73412114
strand: 1
-
alleles:
- ATGTATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412121
feature_type: variation
id: rs1230802347
seq_region_name: 17
source: dbSNP
start: 73412114
strand: 1
-
alleles:
- TGT
- TGTGTATGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412117
feature_type: variation
id: rs1199317711
seq_region_name: 17
source: dbSNP
start: 73412115
strand: 1
-
alleles:
- TGTATACGTATATATGTGTATGTGTATA
- TGTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412142
feature_type: variation
id: rs770403103
seq_region_name: 17
source: dbSNP
start: 73412115
strand: 1
-
alleles:
- "-"
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412115
feature_type: variation
id: rs2063141656
seq_region_name: 17
source: dbSNP
start: 73412116
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412116
feature_type: variation
id: rs1599540562
seq_region_name: 17
source: dbSNP
start: 73412116
strand: 1
-
alleles:
- GTATACGTATA
- GTATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412126
feature_type: variation
id: rs1257358777
seq_region_name: 17
source: dbSNP
start: 73412116
strand: 1
-
alleles:
- TATA
- TATATATGTATACGTATATATA
- TATATGTATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412120
feature_type: variation
id: rs1295677808
seq_region_name: 17
source: dbSNP
start: 73412117
strand: 1
-
alleles:
- TATACGTATATATGTGTAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412135
feature_type: variation
id: rs2063141735
seq_region_name: 17
source: dbSNP
start: 73412117
strand: 1
-
alleles:
- "-"
- GC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412117
feature_type: variation
id: rs2063141756
seq_region_name: 17
source: dbSNP
start: 73412118
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412118
feature_type: variation
id: rs62072149
seq_region_name: 17
source: dbSNP
start: 73412118
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412121
feature_type: variation
id: rs1341273551
seq_region_name: 17
source: dbSNP
start: 73412118
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412119
feature_type: variation
id: rs1288736686
seq_region_name: 17
source: dbSNP
start: 73412119
strand: 1
-
alleles:
- TACGTATATATGTGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412134
feature_type: variation
id: rs1349701971
seq_region_name: 17
source: dbSNP
start: 73412119
strand: 1
-
alleles:
- TACGTATATATGTGTATGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412137
feature_type: variation
id: rs2063141894
seq_region_name: 17
source: dbSNP
start: 73412119
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412120
feature_type: variation
id: rs2063141918
seq_region_name: 17
source: dbSNP
start: 73412120
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412121
feature_type: variation
id: rs1293907369
seq_region_name: 17
source: dbSNP
start: 73412120
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412121
feature_type: variation
id: rs62072150
seq_region_name: 17
source: dbSNP
start: 73412121
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412122
feature_type: variation
id: rs1415062765
seq_region_name: 17
source: dbSNP
start: 73412122
strand: 1
-
alleles:
- TATATAT
- TAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412129
feature_type: variation
id: rs1568389579
seq_region_name: 17
source: dbSNP
start: 73412123
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412124
feature_type: variation
id: rs62072151
seq_region_name: 17
source: dbSNP
start: 73412124
strand: 1
-
alleles:
- TATATGTGTATGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412137
feature_type: variation
id: rs1568389583
seq_region_name: 17
source: dbSNP
start: 73412125
strand: 1
-
alleles:
- TATATGTGTATGTGTATATGT
- TATATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412145
feature_type: variation
id: rs1568389586
seq_region_name: 17
source: dbSNP
start: 73412125
strand: 1
-
alleles:
- TATGTGTATGTGTAT
- TATGTGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412141
feature_type: variation
id: rs2063142229
seq_region_name: 17
source: dbSNP
start: 73412127
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412128
feature_type: variation
id: rs1157088082
seq_region_name: 17
source: dbSNP
start: 73412128
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412129
feature_type: variation
id: rs2063142278
seq_region_name: 17
source: dbSNP
start: 73412129
strand: 1
-
alleles:
- TGTGT
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412133
feature_type: variation
id: rs1456892921
seq_region_name: 17
source: dbSNP
start: 73412129
strand: 1
-
alleles:
- TGTGTATGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412139
feature_type: variation
id: rs1568389594
seq_region_name: 17
source: dbSNP
start: 73412129
strand: 1
-
alleles:
- "-"
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412129
feature_type: variation
id: rs2063142355
seq_region_name: 17
source: dbSNP
start: 73412130
strand: 1
-
alleles:
- GTG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412132
feature_type: variation
id: rs2063142388
seq_region_name: 17
source: dbSNP
start: 73412130
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412131
feature_type: variation
id: rs1843026989
seq_region_name: 17
source: dbSNP
start: 73412131
strand: 1
-
alleles:
- TGTATGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412137
feature_type: variation
id: rs2063142409
seq_region_name: 17
source: dbSNP
start: 73412131
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412132
feature_type: variation
id: rs62072152
seq_region_name: 17
source: dbSNP
start: 73412132
strand: 1
-
alleles:
- "-"
- ACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412132
feature_type: variation
id: rs2063142459
seq_region_name: 17
source: dbSNP
start: 73412133
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412133
feature_type: variation
id: rs1555764380
seq_region_name: 17
source: dbSNP
start: 73412133
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412133
feature_type: variation
id: rs2063142482
seq_region_name: 17
source: dbSNP
start: 73412133
strand: 1
-
alleles:
- TAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412135
feature_type: variation
id: rs1568389600
seq_region_name: 17
source: dbSNP
start: 73412133
strand: 1
-
alleles:
- TATGTGTATATGT
- TATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412145
feature_type: variation
id: rs2063142537
seq_region_name: 17
source: dbSNP
start: 73412133
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412135
feature_type: variation
id: rs1429933330
seq_region_name: 17
source: dbSNP
start: 73412135
strand: 1
-
alleles:
- TGTGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412139
feature_type: variation
id: rs2063142578
seq_region_name: 17
source: dbSNP
start: 73412135
strand: 1
-
alleles:
- TGTGTATATGTATATATACGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412155
feature_type: variation
id: rs1555764383
seq_region_name: 17
source: dbSNP
start: 73412135
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412136
feature_type: variation
id: rs62072153
seq_region_name: 17
source: dbSNP
start: 73412136
strand: 1
-
alleles:
- TGTATAT
- TGTATATATGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412143
feature_type: variation
id: rs2063142651
seq_region_name: 17
source: dbSNP
start: 73412137
strand: 1
-
alleles:
- TGTATATGTAT
- TGTATATGTATGTATATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412147
feature_type: variation
id: rs2063142672
seq_region_name: 17
source: dbSNP
start: 73412137
strand: 1
-
alleles:
- TGTATATGTATATAT
- TGTATATGTATATATGTATATGTATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs1186248865
seq_region_name: 17
source: dbSNP
start: 73412137
strand: 1
-
alleles:
- "-"
- ACAC
- ATATATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412137
feature_type: variation
id: rs1186355535
seq_region_name: 17
source: dbSNP
start: 73412138
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412138
feature_type: variation
id: rs1389152795
seq_region_name: 17
source: dbSNP
start: 73412138
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412139
feature_type: variation
id: rs2063142786
seq_region_name: 17
source: dbSNP
start: 73412139
strand: 1
-
alleles:
- TATAT
- TATATATGTATATATACACATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412143
feature_type: variation
id: rs2063142812
seq_region_name: 17
source: dbSNP
start: 73412139
strand: 1
-
alleles:
- TATATGTATATAT
- TATATGTATATATGTATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs2063142836
seq_region_name: 17
source: dbSNP
start: 73412139
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412140
feature_type: variation
id: rs2048312410
seq_region_name: 17
source: dbSNP
start: 73412140
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412141
feature_type: variation
id: rs2063142853
seq_region_name: 17
source: dbSNP
start: 73412141
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412143
feature_type: variation
id: rs2063142879
seq_region_name: 17
source: dbSNP
start: 73412143
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412145
feature_type: variation
id: rs2063142905
seq_region_name: 17
source: dbSNP
start: 73412145
strand: 1
-
alleles:
- TATATAT
- TATATATGTATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs1568389620
seq_region_name: 17
source: dbSNP
start: 73412145
strand: 1
-
alleles:
- TATATATA
- TATA
- TATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412152
feature_type: variation
id: rs1568389623
seq_region_name: 17
source: dbSNP
start: 73412145
strand: 1
-
alleles:
- ATATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412153
feature_type: variation
id: rs1857118906
seq_region_name: 17
source: dbSNP
start: 73412146
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412147
feature_type: variation
id: rs12946990
seq_region_name: 17
source: dbSNP
start: 73412147
strand: 1
-
alleles:
- TATATACGTATATATGTATATAC
- TATATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412169
feature_type: variation
id: rs1449293825
seq_region_name: 17
source: dbSNP
start: 73412147
strand: 1
-
alleles:
- TAT
- TATGTAT
- TATGTATATGTAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs1257639260
seq_region_name: 17
source: dbSNP
start: 73412149
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412150
feature_type: variation
id: rs1203073066
seq_region_name: 17
source: dbSNP
start: 73412150
strand: 1
-
alleles:
- ATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412153
feature_type: variation
id: rs2063143124
seq_region_name: 17
source: dbSNP
start: 73412150
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs1164566687
seq_region_name: 17
source: dbSNP
start: 73412151
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs2063143140
seq_region_name: 17
source: dbSNP
start: 73412151
strand: 1
-
alleles:
- TACGTA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412156
feature_type: variation
id: rs1328047019
seq_region_name: 17
source: dbSNP
start: 73412151
strand: 1
-
alleles:
- "-"
- GTATATGTATATAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412151
feature_type: variation
id: rs1568389637
seq_region_name: 17
source: dbSNP
start: 73412152
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412152
feature_type: variation
id: rs1599540722
seq_region_name: 17
source: dbSNP
start: 73412152
strand: 1
-
alleles:
- AC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412153
feature_type: variation
id: rs376070533
seq_region_name: 17
source: dbSNP
start: 73412152
strand: 1
-
alleles:
- AC
- ACAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412153
feature_type: variation
id: rs746198515
seq_region_name: 17
source: dbSNP
start: 73412152
strand: 1
-
alleles:
- ACG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412154
feature_type: variation
id: rs1568389649
seq_region_name: 17
source: dbSNP
start: 73412152
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412153
feature_type: variation
id: rs12938460
seq_region_name: 17
source: dbSNP
start: 73412153
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412153
feature_type: variation
id: rs1456788027
seq_region_name: 17
source: dbSNP
start: 73412153
strand: 1
-
alleles:
- CG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412154
feature_type: variation
id: rs1568389659
seq_region_name: 17
source: dbSNP
start: 73412153
strand: 1
-
alleles:
- CGTATATATG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412162
feature_type: variation
id: rs1229941698
seq_region_name: 17
source: dbSNP
start: 73412153
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412154
feature_type: variation
id: rs1283485490
seq_region_name: 17
source: dbSNP
start: 73412154
strand: 1
-
alleles:
- GT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412155
feature_type: variation
id: rs2063143407
seq_region_name: 17
source: dbSNP
start: 73412154
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412155
feature_type: variation
id: rs1448630214
seq_region_name: 17
source: dbSNP
start: 73412155
strand: 1
-
alleles:
- TATATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412161
feature_type: variation
id: rs1568389668
seq_region_name: 17
source: dbSNP
start: 73412155
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412156
feature_type: variation
id: rs969448734
seq_region_name: 17
source: dbSNP
start: 73412156
strand: 1
-
alleles:
- ATATATGTATATACACATATATGTATAT
- ATATATGTATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412183
feature_type: variation
id: rs1568389677
seq_region_name: 17
source: dbSNP
start: 73412156
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412157
feature_type: variation
id: rs2063143520
seq_region_name: 17
source: dbSNP
start: 73412157
strand: 1
-
alleles:
- TATATGTATAT
- TATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412167
feature_type: variation
id: rs1385852012
seq_region_name: 17
source: dbSNP
start: 73412157
strand: 1
-
alleles:
- TATGTAT
- TAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412165
feature_type: variation
id: rs1437355825
seq_region_name: 17
source: dbSNP
start: 73412159
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412160
feature_type: variation
id: rs62072154
seq_region_name: 17
source: dbSNP
start: 73412160
strand: 1
-
alleles:
- "-"
- CG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412160
feature_type: variation
id: rs1434726084
seq_region_name: 17
source: dbSNP
start: 73412161
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412161
feature_type: variation
id: rs1460154430
seq_region_name: 17
source: dbSNP
start: 73412161
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412163
feature_type: variation
id: rs2063143756
seq_region_name: 17
source: dbSNP
start: 73412161
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412162
feature_type: variation
id: rs62072155
seq_region_name: 17
source: dbSNP
start: 73412162
strand: 1
-
alleles:
- GTATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412169
feature_type: variation
id: rs2063143845
seq_region_name: 17
source: dbSNP
start: 73412162
strand: 1
-
alleles:
- "-"
- CA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412162
feature_type: variation
id: rs2063143881
seq_region_name: 17
source: dbSNP
start: 73412163
strand: 1
-
alleles:
- TATAT
- TATATGCATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412167
feature_type: variation
id: rs2063143920
seq_region_name: 17
source: dbSNP
start: 73412163
strand: 1
-
alleles:
- TATATA
- TATA
- TATATATA
- TATATATACACATATATGTATATATA
- TATATATACACATATATGTATATATACGTATATATGTATATATA
- TATATATATA
- TATATATGTATATGTATATATACGTATATATGTATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412168
feature_type: variation
id: rs202158962
seq_region_name: 17
source: dbSNP
start: 73412163
strand: 1
-
alleles:
- A
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412164
feature_type: variation
id: rs1474053581
seq_region_name: 17
source: dbSNP
start: 73412164
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412164
feature_type: variation
id: rs2063144038
seq_region_name: 17
source: dbSNP
start: 73412164
strand: 1
-
alleles:
- TATACACATATATGTATA
- TATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412182
feature_type: variation
id: rs2063144103
seq_region_name: 17
source: dbSNP
start: 73412165
strand: 1
-
alleles:
- A
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412166
feature_type: variation
id: rs2063144121
seq_region_name: 17
source: dbSNP
start: 73412166
strand: 1
-
alleles:
- T
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412167
feature_type: variation
id: rs1568389704
seq_region_name: 17
source: dbSNP
start: 73412167
strand: 1
-
alleles:
- "-"
- GC
- GCACATAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412167
feature_type: variation
id: rs1369766105
seq_region_name: 17
source: dbSNP
start: 73412168
strand: 1
-
alleles:
- A
- ATACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412168
feature_type: variation
id: rs2063144180
seq_region_name: 17
source: dbSNP
start: 73412168
strand: 1
-
alleles:
- ACACA
- ACACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412172
feature_type: variation
id: rs2063144197
seq_region_name: 17
source: dbSNP
start: 73412168
strand: 1
-
alleles:
- ACACATATATGTATATGCACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412188
feature_type: variation
id: rs2063144215
seq_region_name: 17
source: dbSNP
start: 73412168
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412169
feature_type: variation
id: rs368788823
seq_region_name: 17
source: dbSNP
start: 73412169
strand: 1
-
alleles:
- A
- ATACACACATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412170
feature_type: variation
id: rs1568389711
seq_region_name: 17
source: dbSNP
start: 73412170
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412170
feature_type: variation
id: rs2063144262
seq_region_name: 17
source: dbSNP
start: 73412170
strand: 1
-
alleles:
- ACATATATGTATATGCACATACACACATATACATATATGTATATGCA
- ACATATATGTATATGCACATACACACATATACATATATGTATATGCACATACACACATATACATATATGTATATGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412216
feature_type: variation
id: rs1568389714
seq_region_name: 17
source: dbSNP
start: 73412170
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412171
feature_type: variation
id: rs2063144334
seq_region_name: 17
source: dbSNP
start: 73412171
strand: 1
-
alleles:
- "-"
- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412171
feature_type: variation
id: rs1246476476
seq_region_name: 17
source: dbSNP
start: 73412172
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412172
feature_type: variation
id: rs2145562404
seq_region_name: 17
source: dbSNP
start: 73412172
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412173
feature_type: variation
id: rs528598602
seq_region_name: 17
source: dbSNP
start: 73412173
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412174
feature_type: variation
id: rs2063144394
seq_region_name: 17
source: dbSNP
start: 73412174
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412178
feature_type: variation
id: rs915516894
seq_region_name: 17
source: dbSNP
start: 73412178
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412179
feature_type: variation
id: rs2063144441
seq_region_name: 17
source: dbSNP
start: 73412179
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412183
feature_type: variation
id: rs1467001209
seq_region_name: 17
source: dbSNP
start: 73412183
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412184
feature_type: variation
id: rs2063144493
seq_region_name: 17
source: dbSNP
start: 73412184
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412185
feature_type: variation
id: rs1261235684
seq_region_name: 17
source: dbSNP
start: 73412185
strand: 1
-
alleles:
- CA
- CATATACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412186
feature_type: variation
id: rs2063144525
seq_region_name: 17
source: dbSNP
start: 73412185
strand: 1
-
alleles:
- CACA
- CA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412188
feature_type: variation
id: rs530960557
seq_region_name: 17
source: dbSNP
start: 73412185
strand: 1
-
alleles:
- "-"
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412186
feature_type: variation
id: rs1358374643
seq_region_name: 17
source: dbSNP
start: 73412187
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412187
feature_type: variation
id: rs1268494613
seq_region_name: 17
source: dbSNP
start: 73412187
strand: 1
-
alleles:
- CATACACACATATACATATATGTATATGCATA
- CATACACACATATACATATATGTATATGCATACACACATATACATATATGTATATGCATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412218
feature_type: variation
id: rs2063144617
seq_region_name: 17
source: dbSNP
start: 73412187
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412189
feature_type: variation
id: rs1015594279
seq_region_name: 17
source: dbSNP
start: 73412189
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412189
feature_type: variation
id: rs1366223727
seq_region_name: 17
source: dbSNP
start: 73412189
strand: 1
-
alleles:
- ACACACA
- ACA
- ACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412196
feature_type: variation
id: rs1438960749
seq_region_name: 17
source: dbSNP
start: 73412190
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412191
feature_type: variation
id: rs543483389
seq_region_name: 17
source: dbSNP
start: 73412191
strand: 1
-
alleles:
- ACACATATACA
- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412202
feature_type: variation
id: rs2063144731
seq_region_name: 17
source: dbSNP
start: 73412192
strand: 1
-
alleles:
- ACACATATACATATATGTATATGCA
- ACACATATACATATATGTATATGCACATACACATATACATATATGTATATGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412216
feature_type: variation
id: rs2063144745
seq_region_name: 17
source: dbSNP
start: 73412192
strand: 1
-
alleles:
- ACACATATACATATATGTATATGCATATACACATATACATATAT
- ACACATATACATATAT
- ACACATATACATATATGTATATGCATATACACATATACATATATGTATATGCATATACACATATACATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412235
feature_type: variation
id: rs573210455
seq_region_name: 17
source: dbSNP
start: 73412192
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412193
feature_type: variation
id: rs1407583143
seq_region_name: 17
source: dbSNP
start: 73412193
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412194
feature_type: variation
id: rs1166200279
seq_region_name: 17
source: dbSNP
start: 73412194
strand: 1
-
alleles:
- ACATA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412198
feature_type: variation
id: rs1417923774
seq_region_name: 17
source: dbSNP
start: 73412194
strand: 1
-
alleles:
- ACATATACATATA
- ACATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412206
feature_type: variation
id: rs2063144860
seq_region_name: 17
source: dbSNP
start: 73412194
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412195
feature_type: variation
id: rs1206257242
seq_region_name: 17
source: dbSNP
start: 73412195
strand: 1
-
alleles:
- ATATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412200
feature_type: variation
id: rs1390224040
seq_region_name: 17
source: dbSNP
start: 73412196
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412197
feature_type: variation
id: rs2063144924
seq_region_name: 17
source: dbSNP
start: 73412197
strand: 1
-
alleles:
- ATACATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412204
feature_type: variation
id: rs745548102
seq_region_name: 17
source: dbSNP
start: 73412198
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412203
feature_type: variation
id: rs946842982
seq_region_name: 17
source: dbSNP
start: 73412203
strand: 1
-
alleles:
- TATATGTATATG
- TATATGTATATGTATATG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412214
feature_type: variation
id: rs2063144997
seq_region_name: 17
source: dbSNP
start: 73412203
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412204
feature_type: variation
id: rs1476828638
seq_region_name: 17
source: dbSNP
start: 73412204
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412205
feature_type: variation
id: rs2063145038
seq_region_name: 17
source: dbSNP
start: 73412205
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412206
feature_type: variation
id: rs1245977582
seq_region_name: 17
source: dbSNP
start: 73412206
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412207
feature_type: variation
id: rs1039878154
seq_region_name: 17
source: dbSNP
start: 73412207
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412209
feature_type: variation
id: rs1453268293
seq_region_name: 17
source: dbSNP
start: 73412209
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412210
feature_type: variation
id: rs2063145111
seq_region_name: 17
source: dbSNP
start: 73412210
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412212
feature_type: variation
id: rs2063145129
seq_region_name: 17
source: dbSNP
start: 73412212
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412212
feature_type: variation
id: rs2063145147
seq_region_name: 17
source: dbSNP
start: 73412212
strand: 1
-
alleles:
- GCATATAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412221
feature_type: variation
id: rs2063145174
seq_region_name: 17
source: dbSNP
start: 73412214
strand: 1
-
alleles:
- CA
- CACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412216
feature_type: variation
id: rs2063145199
seq_region_name: 17
source: dbSNP
start: 73412215
strand: 1
-
alleles:
- CATATACACATATACA
- CATATACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412230
feature_type: variation
id: rs919623439
seq_region_name: 17
source: dbSNP
start: 73412215
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412217
feature_type: variation
id: rs1204560111
seq_region_name: 17
source: dbSNP
start: 73412217
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412219
feature_type: variation
id: rs1343029951
seq_region_name: 17
source: dbSNP
start: 73412219
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412221
feature_type: variation
id: rs1299907097
seq_region_name: 17
source: dbSNP
start: 73412221
strand: 1
-
alleles:
- ACATATACATATATACATATA
- ACATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412242
feature_type: variation
id: rs1232456303
seq_region_name: 17
source: dbSNP
start: 73412222
strand: 1
-
alleles:
- ATATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412228
feature_type: variation
id: rs931048074
seq_region_name: 17
source: dbSNP
start: 73412224
strand: 1
-
alleles:
- ATATACATATATACATATAT
- ATATACATATAT
- ATATACATATATACATATATACATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412243
feature_type: variation
id: rs1258623482
seq_region_name: 17
source: dbSNP
start: 73412224
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412225
feature_type: variation
id: rs1422429771
seq_region_name: 17
source: dbSNP
start: 73412225
strand: 1
-
alleles:
- ATACATA
- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412232
feature_type: variation
id: rs1353302005
seq_region_name: 17
source: dbSNP
start: 73412226
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412227
feature_type: variation
id: rs1308006147
seq_region_name: 17
source: dbSNP
start: 73412227
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412228
feature_type: variation
id: rs546748756
seq_region_name: 17
source: dbSNP
start: 73412228
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412231
feature_type: variation
id: rs568453945
seq_region_name: 17
source: dbSNP
start: 73412231
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412232
feature_type: variation
id: rs2063145502
seq_region_name: 17
source: dbSNP
start: 73412232
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412235
feature_type: variation
id: rs2063145524
seq_region_name: 17
source: dbSNP
start: 73412235
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412238
feature_type: variation
id: rs535344887
seq_region_name: 17
source: dbSNP
start: 73412238
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412239
feature_type: variation
id: rs2063145568
seq_region_name: 17
source: dbSNP
start: 73412239
strand: 1
-
alleles:
- A
- ACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412242
feature_type: variation
id: rs2063145592
seq_region_name: 17
source: dbSNP
start: 73412242
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412244
feature_type: variation
id: rs1156979595
seq_region_name: 17
source: dbSNP
start: 73412244
strand: 1
-
alleles:
- TGGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412249
feature_type: variation
id: rs2063145629
seq_region_name: 17
source: dbSNP
start: 73412246
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412249
feature_type: variation
id: rs2063145653
seq_region_name: 17
source: dbSNP
start: 73412249
strand: 1
-
alleles:
- ACATATACATATACATATA
- ACATATACATATA
- ACATATACATATACATATACATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412268
feature_type: variation
id: rs776010834
seq_region_name: 17
source: dbSNP
start: 73412250
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412251
feature_type: variation
id: rs766349844
seq_region_name: 17
source: dbSNP
start: 73412251
strand: 1
-
alleles:
- ATATA
- ATATATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412256
feature_type: variation
id: rs2063145743
seq_region_name: 17
source: dbSNP
start: 73412252
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412253
feature_type: variation
id: rs1423956998
seq_region_name: 17
source: dbSNP
start: 73412253
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412255
feature_type: variation
id: rs2063145780
seq_region_name: 17
source: dbSNP
start: 73412255
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412257
feature_type: variation
id: rs2063145794
seq_region_name: 17
source: dbSNP
start: 73412257
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412258
feature_type: variation
id: rs1191577744
seq_region_name: 17
source: dbSNP
start: 73412258
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412259
feature_type: variation
id: rs2063145843
seq_region_name: 17
source: dbSNP
start: 73412259
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412261
feature_type: variation
id: rs2063145858
seq_region_name: 17
source: dbSNP
start: 73412261
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412262
feature_type: variation
id: rs2063145884
seq_region_name: 17
source: dbSNP
start: 73412262
strand: 1
-
alleles:
- ACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412264
feature_type: variation
id: rs2063145906
seq_region_name: 17
source: dbSNP
start: 73412262
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412264
feature_type: variation
id: rs2063145933
seq_region_name: 17
source: dbSNP
start: 73412264
strand: 1
-
alleles:
- ATATATATAT
- ATATATAT
- ATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412273
feature_type: variation
id: rs1249305455
seq_region_name: 17
source: dbSNP
start: 73412264
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412266
feature_type: variation
id: rs1599541010
seq_region_name: 17
source: dbSNP
start: 73412266
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412272
feature_type: variation
id: rs183451618
seq_region_name: 17
source: dbSNP
start: 73412272
strand: 1
-
alleles:
- TGTGTGTGTGTGT
- TGTGTGTGTGT
- TGTGTGTGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412285
feature_type: variation
id: rs199817011
seq_region_name: 17
source: dbSNP
start: 73412273
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412274
feature_type: variation
id: rs2063146066
seq_region_name: 17
source: dbSNP
start: 73412274
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412278
feature_type: variation
id: rs2145562905
seq_region_name: 17
source: dbSNP
start: 73412278
strand: 1
-
alleles:
- TGTGTGTATATATATATGTGTGTATATATATAT
- TGTGTGTATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412311
feature_type: variation
id: rs1304371901
seq_region_name: 17
source: dbSNP
start: 73412279
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412281
feature_type: variation
id: rs2063146102
seq_region_name: 17
source: dbSNP
start: 73412281
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412282
feature_type: variation
id: rs2063146124
seq_region_name: 17
source: dbSNP
start: 73412282
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412284
feature_type: variation
id: rs946017731
seq_region_name: 17
source: dbSNP
start: 73412284
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412285
feature_type: variation
id: rs1371693796
seq_region_name: 17
source: dbSNP
start: 73412285
strand: 1
-
alleles:
- TATATATATAT
- TATATAT
- TATATATAT
- TATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412295
feature_type: variation
id: rs113442771
seq_region_name: 17
source: dbSNP
start: 73412285
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412286
feature_type: variation
id: rs1004784940
seq_region_name: 17
source: dbSNP
start: 73412286
strand: 1
-
alleles:
- TATATATATGTGTGTATATATAT
- TATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412309
feature_type: variation
id: rs996239377
seq_region_name: 17
source: dbSNP
start: 73412287
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412291
feature_type: variation
id: rs1204313450
seq_region_name: 17
source: dbSNP
start: 73412291
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412292
feature_type: variation
id: rs2145562954
seq_region_name: 17
source: dbSNP
start: 73412292
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412293
feature_type: variation
id: rs2063146292
seq_region_name: 17
source: dbSNP
start: 73412293
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412294
feature_type: variation
id: rs563659229
seq_region_name: 17
source: dbSNP
start: 73412294
strand: 1
-
alleles:
- TGTGTGT
- TGTGTGTGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412301
feature_type: variation
id: rs2063146345
seq_region_name: 17
source: dbSNP
start: 73412295
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412296
feature_type: variation
id: rs899090641
seq_region_name: 17
source: dbSNP
start: 73412296
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412297
feature_type: variation
id: rs995040092
seq_region_name: 17
source: dbSNP
start: 73412297
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412298
feature_type: variation
id: rs568804849
seq_region_name: 17
source: dbSNP
start: 73412298
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412300
feature_type: variation
id: rs1176382908
seq_region_name: 17
source: dbSNP
start: 73412300
strand: 1
-
alleles:
- TATATATATATAT
- TATATATATAT
- TATATATATATATAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412313
feature_type: variation
id: rs1009477537
seq_region_name: 17
source: dbSNP
start: 73412301
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1015128864
seq_region_name: 17
source: dbSNP
start: 73412302
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063146475
seq_region_name: 17
source: dbSNP
start: 73412304
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1158062530
seq_region_name: 17
source: dbSNP
start: 73412308
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412312
feature_type: variation
id: rs962596487
seq_region_name: 17
source: dbSNP
start: 73412312
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412314
feature_type: variation
id: rs969437399
seq_region_name: 17
source: dbSNP
start: 73412314
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412319
feature_type: variation
id: rs2063146559
seq_region_name: 17
source: dbSNP
start: 73412319
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412321
feature_type: variation
id: rs2063146579
seq_region_name: 17
source: dbSNP
start: 73412321
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412322
feature_type: variation
id: rs1026586687
seq_region_name: 17
source: dbSNP
start: 73412322
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412324
feature_type: variation
id: rs2063146628
seq_region_name: 17
source: dbSNP
start: 73412324
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412325
feature_type: variation
id: rs982191863
seq_region_name: 17
source: dbSNP
start: 73412325
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412330
feature_type: variation
id: rs2063146672
seq_region_name: 17
source: dbSNP
start: 73412330
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412334
feature_type: variation
id: rs539309477
seq_region_name: 17
source: dbSNP
start: 73412334
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412335
feature_type: variation
id: rs952396764
seq_region_name: 17
source: dbSNP
start: 73412335
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412338
feature_type: variation
id: rs2063146744
seq_region_name: 17
source: dbSNP
start: 73412338
strand: 1
-
alleles:
- CCAGGCTGGTCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412356
feature_type: variation
id: rs1212582923
seq_region_name: 17
source: dbSNP
start: 73412345
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412347
feature_type: variation
id: rs1327333803
seq_region_name: 17
source: dbSNP
start: 73412347
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412359
feature_type: variation
id: rs2063146803
seq_region_name: 17
source: dbSNP
start: 73412359
strand: 1
-
alleles:
- AACTCCCAACCTCAGGTAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412377
feature_type: variation
id: rs2063146827
seq_region_name: 17
source: dbSNP
start: 73412359
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412361
feature_type: variation
id: rs2145563121
seq_region_name: 17
source: dbSNP
start: 73412361
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412367
feature_type: variation
id: rs377388731
seq_region_name: 17
source: dbSNP
start: 73412367
strand: 1
-
alleles:
- CTC
- CTCTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412371
feature_type: variation
id: rs1775640685
seq_region_name: 17
source: dbSNP
start: 73412369
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412370
feature_type: variation
id: rs2063146886
seq_region_name: 17
source: dbSNP
start: 73412370
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412372
feature_type: variation
id: rs1235375613
seq_region_name: 17
source: dbSNP
start: 73412372
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412374
feature_type: variation
id: rs1034967220
seq_region_name: 17
source: dbSNP
start: 73412374
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412375
feature_type: variation
id: rs1599541102
seq_region_name: 17
source: dbSNP
start: 73412375
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412377
feature_type: variation
id: rs2063146962
seq_region_name: 17
source: dbSNP
start: 73412377
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412378
feature_type: variation
id: rs2145563167
seq_region_name: 17
source: dbSNP
start: 73412378
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412379
feature_type: variation
id: rs1291930434
seq_region_name: 17
source: dbSNP
start: 73412379
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412380
feature_type: variation
id: rs9905651
seq_region_name: 17
source: dbSNP
start: 73412380
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412385
feature_type: variation
id: rs572675021
seq_region_name: 17
source: dbSNP
start: 73412385
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412386
feature_type: variation
id: rs1302918037
seq_region_name: 17
source: dbSNP
start: 73412386
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412387
feature_type: variation
id: rs915442380
seq_region_name: 17
source: dbSNP
start: 73412387
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412393
feature_type: variation
id: rs946991156
seq_region_name: 17
source: dbSNP
start: 73412393
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412398
feature_type: variation
id: rs755152791
seq_region_name: 17
source: dbSNP
start: 73412398
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412403
feature_type: variation
id: rs1181609215
seq_region_name: 17
source: dbSNP
start: 73412403
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412404
feature_type: variation
id: rs1251911967
seq_region_name: 17
source: dbSNP
start: 73412404
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412413
feature_type: variation
id: rs1473828252
seq_region_name: 17
source: dbSNP
start: 73412413
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412418
feature_type: variation
id: rs2063147173
seq_region_name: 17
source: dbSNP
start: 73412418
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412420
feature_type: variation
id: rs2063147196
seq_region_name: 17
source: dbSNP
start: 73412420
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412423
feature_type: variation
id: rs927045374
seq_region_name: 17
source: dbSNP
start: 73412423
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412428
feature_type: variation
id: rs2063147245
seq_region_name: 17
source: dbSNP
start: 73412428
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412431
feature_type: variation
id: rs2145563267
seq_region_name: 17
source: dbSNP
start: 73412431
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412435
feature_type: variation
id: rs959853926
seq_region_name: 17
source: dbSNP
start: 73412435
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412437
feature_type: variation
id: rs1707897858
seq_region_name: 17
source: dbSNP
start: 73412437
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412438
feature_type: variation
id: rs993061701
seq_region_name: 17
source: dbSNP
start: 73412438
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412439
feature_type: variation
id: rs2063147269
seq_region_name: 17
source: dbSNP
start: 73412439
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412441
feature_type: variation
id: rs1457539535
seq_region_name: 17
source: dbSNP
start: 73412441
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412443
feature_type: variation
id: rs533903075
seq_region_name: 17
source: dbSNP
start: 73412443
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412445
feature_type: variation
id: rs2063147359
seq_region_name: 17
source: dbSNP
start: 73412445
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412448
feature_type: variation
id: rs2063147393
seq_region_name: 17
source: dbSNP
start: 73412448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412449
feature_type: variation
id: rs975982707
seq_region_name: 17
source: dbSNP
start: 73412449
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412452
feature_type: variation
id: rs1162657656
seq_region_name: 17
source: dbSNP
start: 73412452
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412454
feature_type: variation
id: rs1568389946
seq_region_name: 17
source: dbSNP
start: 73412454
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412459
feature_type: variation
id: rs921464972
seq_region_name: 17
source: dbSNP
start: 73412459
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412462
feature_type: variation
id: rs2145563346
seq_region_name: 17
source: dbSNP
start: 73412462
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412464
feature_type: variation
id: rs931706021
seq_region_name: 17
source: dbSNP
start: 73412464
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412468
feature_type: variation
id: rs1414706300
seq_region_name: 17
source: dbSNP
start: 73412468
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412471
feature_type: variation
id: rs1051533999
seq_region_name: 17
source: dbSNP
start: 73412471
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412475
feature_type: variation
id: rs1183604098
seq_region_name: 17
source: dbSNP
start: 73412475
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412477
feature_type: variation
id: rs2063147584
seq_region_name: 17
source: dbSNP
start: 73412477
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412479
feature_type: variation
id: rs1463723935
seq_region_name: 17
source: dbSNP
start: 73412479
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412482
feature_type: variation
id: rs118176764
seq_region_name: 17
source: dbSNP
start: 73412482
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412483
feature_type: variation
id: rs2063147667
seq_region_name: 17
source: dbSNP
start: 73412483
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412484
feature_type: variation
id: rs2063147695
seq_region_name: 17
source: dbSNP
start: 73412484
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412486
feature_type: variation
id: rs1209777815
seq_region_name: 17
source: dbSNP
start: 73412486
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412494
feature_type: variation
id: rs945935208
seq_region_name: 17
source: dbSNP
start: 73412494
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412498
feature_type: variation
id: rs940316508
seq_region_name: 17
source: dbSNP
start: 73412498
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412507
feature_type: variation
id: rs1568389980
seq_region_name: 17
source: dbSNP
start: 73412507
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412509
feature_type: variation
id: rs1043012576
seq_region_name: 17
source: dbSNP
start: 73412509
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412512
feature_type: variation
id: rs2063147794
seq_region_name: 17
source: dbSNP
start: 73412512
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412514
feature_type: variation
id: rs1411244147
seq_region_name: 17
source: dbSNP
start: 73412514
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412515
feature_type: variation
id: rs2145563461
seq_region_name: 17
source: dbSNP
start: 73412515
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412517
feature_type: variation
id: rs2145563466
seq_region_name: 17
source: dbSNP
start: 73412517
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412518
feature_type: variation
id: rs2063147844
seq_region_name: 17
source: dbSNP
start: 73412518
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412520
feature_type: variation
id: rs1312833343
seq_region_name: 17
source: dbSNP
start: 73412520
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412524
feature_type: variation
id: rs2063147882
seq_region_name: 17
source: dbSNP
start: 73412524
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412526
feature_type: variation
id: rs1247477672
seq_region_name: 17
source: dbSNP
start: 73412526
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412527
feature_type: variation
id: rs2063147898
seq_region_name: 17
source: dbSNP
start: 73412527
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412528
feature_type: variation
id: rs371392854
seq_region_name: 17
source: dbSNP
start: 73412528
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412529
feature_type: variation
id: rs2063147948
seq_region_name: 17
source: dbSNP
start: 73412529
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412534
feature_type: variation
id: rs1036032023
seq_region_name: 17
source: dbSNP
start: 73412534
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412536
feature_type: variation
id: rs1952948701
seq_region_name: 17
source: dbSNP
start: 73412534
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412535
feature_type: variation
id: rs899077172
seq_region_name: 17
source: dbSNP
start: 73412535
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73412742
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73412745
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73412776
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412780
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs564689346
seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73412930
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73412940
strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412949
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73412955
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73412962
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73412963
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73412964
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73412965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412972
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412973
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
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start: 73412975
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412976
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412982
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73412983
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73412987
feature_type: variation
id: rs2063152161
seq_region_name: 17
source: dbSNP
start: 73412987
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063152192
seq_region_name: 17
source: dbSNP
start: 73412994
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063152229
seq_region_name: 17
source: dbSNP
start: 73412995
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568390234
seq_region_name: 17
source: dbSNP
start: 73412996
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1274603643
seq_region_name: 17
source: dbSNP
start: 73412997
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413001
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413004
feature_type: variation
id: rs1032874794
seq_region_name: 17
source: dbSNP
start: 73413004
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063152369
seq_region_name: 17
source: dbSNP
start: 73413012
strand: 1
-
alleles:
- CCAGGGTTCCCC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413024
feature_type: variation
id: rs1320686020
seq_region_name: 17
source: dbSNP
start: 73413013
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413014
feature_type: variation
id: rs1404100062
seq_region_name: 17
source: dbSNP
start: 73413014
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413015
feature_type: variation
id: rs2063152430
seq_region_name: 17
source: dbSNP
start: 73413015
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413021
feature_type: variation
id: rs2063152449
seq_region_name: 17
source: dbSNP
start: 73413021
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413023
feature_type: variation
id: rs2063152472
seq_region_name: 17
source: dbSNP
start: 73413023
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063152654
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1244989587
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1189518740
seq_region_name: 17
source: dbSNP
start: 73413042
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413045
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413057
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1392233318
seq_region_name: 17
source: dbSNP
start: 73413058
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1447480370
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063152830
seq_region_name: 17
source: dbSNP
start: 73413062
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1361743495
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs911854117
seq_region_name: 17
source: dbSNP
start: 73413066
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063152873
seq_region_name: 17
source: dbSNP
start: 73413067
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs986963748
seq_region_name: 17
source: dbSNP
start: 73413076
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1015805494
seq_region_name: 17
source: dbSNP
start: 73413078
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063152944
seq_region_name: 17
source: dbSNP
start: 73413079
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063152970
seq_region_name: 17
source: dbSNP
start: 73413082
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1272300104
seq_region_name: 17
source: dbSNP
start: 73413083
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413090
feature_type: variation
id: rs2063153015
seq_region_name: 17
source: dbSNP
start: 73413090
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs972520696
seq_region_name: 17
source: dbSNP
start: 73413091
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs962088958
seq_region_name: 17
source: dbSNP
start: 73413093
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413094
feature_type: variation
id: rs971864934
seq_region_name: 17
source: dbSNP
start: 73413094
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413095
feature_type: variation
id: rs539604859
seq_region_name: 17
source: dbSNP
start: 73413095
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413101
feature_type: variation
id: rs2063153115
seq_region_name: 17
source: dbSNP
start: 73413101
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413114
feature_type: variation
id: rs750169288
seq_region_name: 17
source: dbSNP
start: 73413114
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1166104084
seq_region_name: 17
source: dbSNP
start: 73413118
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1321013161
seq_region_name: 17
source: dbSNP
start: 73413119
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs930300311
seq_region_name: 17
source: dbSNP
start: 73413125
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413129
feature_type: variation
id: rs2063153205
seq_region_name: 17
source: dbSNP
start: 73413129
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413143
feature_type: variation
id: rs2063153229
seq_region_name: 17
source: dbSNP
start: 73413143
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413146
feature_type: variation
id: rs980415063
seq_region_name: 17
source: dbSNP
start: 73413146
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413147
feature_type: variation
id: rs544550557
seq_region_name: 17
source: dbSNP
start: 73413147
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413149
feature_type: variation
id: rs2063153275
seq_region_name: 17
source: dbSNP
start: 73413149
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063153303
seq_region_name: 17
source: dbSNP
start: 73413150
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413154
feature_type: variation
id: rs939308919
seq_region_name: 17
source: dbSNP
start: 73413154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413155
feature_type: variation
id: rs2063153342
seq_region_name: 17
source: dbSNP
start: 73413155
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413157
feature_type: variation
id: rs1476940941
seq_region_name: 17
source: dbSNP
start: 73413157
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413160
feature_type: variation
id: rs2063153389
seq_region_name: 17
source: dbSNP
start: 73413160
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413162
feature_type: variation
id: rs2063153409
seq_region_name: 17
source: dbSNP
start: 73413162
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413166
feature_type: variation
id: rs746460002
seq_region_name: 17
source: dbSNP
start: 73413163
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413164
feature_type: variation
id: rs1200130746
seq_region_name: 17
source: dbSNP
start: 73413164
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413167
feature_type: variation
id: rs1599541887
seq_region_name: 17
source: dbSNP
start: 73413167
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413170
feature_type: variation
id: rs1056217847
seq_region_name: 17
source: dbSNP
start: 73413170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413171
feature_type: variation
id: rs2063153523
seq_region_name: 17
source: dbSNP
start: 73413171
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413175
feature_type: variation
id: rs1249715998
seq_region_name: 17
source: dbSNP
start: 73413175
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413176
feature_type: variation
id: rs895436693
seq_region_name: 17
source: dbSNP
start: 73413176
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413185
feature_type: variation
id: rs1599541910
seq_region_name: 17
source: dbSNP
start: 73413185
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413187
feature_type: variation
id: rs1343181671
seq_region_name: 17
source: dbSNP
start: 73413187
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413189
feature_type: variation
id: rs1013924843
seq_region_name: 17
source: dbSNP
start: 73413189
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413196
feature_type: variation
id: rs2063153673
seq_region_name: 17
source: dbSNP
start: 73413196
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413198
feature_type: variation
id: rs2063153692
seq_region_name: 17
source: dbSNP
start: 73413198
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413199
feature_type: variation
id: rs892326068
seq_region_name: 17
source: dbSNP
start: 73413199
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413201
feature_type: variation
id: rs945434146
seq_region_name: 17
source: dbSNP
start: 73413201
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413203
feature_type: variation
id: rs902922081
seq_region_name: 17
source: dbSNP
start: 73413203
strand: 1
-
alleles:
- G
- GAATCCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413203
feature_type: variation
id: rs2145564956
seq_region_name: 17
source: dbSNP
start: 73413203
strand: 1
-
alleles:
- "-"
- AAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413203
feature_type: variation
id: rs2063153794
seq_region_name: 17
source: dbSNP
start: 73413204
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413204
feature_type: variation
id: rs1043793380
seq_region_name: 17
source: dbSNP
start: 73413204
strand: 1
-
alleles:
- "-"
- CTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413204
feature_type: variation
id: rs2063153851
seq_region_name: 17
source: dbSNP
start: 73413205
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413205
feature_type: variation
id: rs903948841
seq_region_name: 17
source: dbSNP
start: 73413205
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413206
feature_type: variation
id: rs1305666853
seq_region_name: 17
source: dbSNP
start: 73413206
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413207
feature_type: variation
id: rs1408643414
seq_region_name: 17
source: dbSNP
start: 73413207
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413210
feature_type: variation
id: rs1354579569
seq_region_name: 17
source: dbSNP
start: 73413210
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413212
feature_type: variation
id: rs2063153959
seq_region_name: 17
source: dbSNP
start: 73413212
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413215
feature_type: variation
id: rs2063153979
seq_region_name: 17
source: dbSNP
start: 73413215
strand: 1
-
alleles:
- CTGTGAACTGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413225
feature_type: variation
id: rs2063154004
seq_region_name: 17
source: dbSNP
start: 73413215
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413216
feature_type: variation
id: rs2063154028
seq_region_name: 17
source: dbSNP
start: 73413216
strand: 1
-
alleles:
- GTGAACTGTGG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413227
feature_type: variation
id: rs2063154054
seq_region_name: 17
source: dbSNP
start: 73413217
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413221
feature_type: variation
id: rs2063154078
seq_region_name: 17
source: dbSNP
start: 73413221
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413225
feature_type: variation
id: rs551229730
seq_region_name: 17
source: dbSNP
start: 73413225
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413226
feature_type: variation
id: rs2063154127
seq_region_name: 17
source: dbSNP
start: 73413226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413227
feature_type: variation
id: rs755948050
seq_region_name: 17
source: dbSNP
start: 73413227
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413229
feature_type: variation
id: rs1032823864
seq_region_name: 17
source: dbSNP
start: 73413229
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413230
feature_type: variation
id: rs2063154174
seq_region_name: 17
source: dbSNP
start: 73413230
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413231
feature_type: variation
id: rs2063154195
seq_region_name: 17
source: dbSNP
start: 73413231
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413235
feature_type: variation
id: rs2063154211
seq_region_name: 17
source: dbSNP
start: 73413235
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413237
feature_type: variation
id: rs1599541979
seq_region_name: 17
source: dbSNP
start: 73413237
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413242
feature_type: variation
id: rs1357679408
seq_region_name: 17
source: dbSNP
start: 73413242
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413243
feature_type: variation
id: rs2063154274
seq_region_name: 17
source: dbSNP
start: 73413242
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413244
feature_type: variation
id: rs779504477
seq_region_name: 17
source: dbSNP
start: 73413244
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413251
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063154471
seq_region_name: 17
source: dbSNP
start: 73413253
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs555484943
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
start: 73413258
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063154605
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413270
strand: 1
-
alleles:
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- TGAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1441993016
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs966398811
seq_region_name: 17
source: dbSNP
start: 73413277
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1225681370
seq_region_name: 17
source: dbSNP
start: 73413287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063154717
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1327743090
seq_region_name: 17
source: dbSNP
start: 73413290
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413292
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063154788
seq_region_name: 17
source: dbSNP
start: 73413303
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs891376345
seq_region_name: 17
source: dbSNP
start: 73413305
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063154835
seq_region_name: 17
source: dbSNP
start: 73413308
strand: 1
-
alleles:
- CGGAC
- CGGACGGAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063154856
seq_region_name: 17
source: dbSNP
start: 73413308
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs150657064
seq_region_name: 17
source: dbSNP
start: 73413309
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1187718110
seq_region_name: 17
source: dbSNP
start: 73413312
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs919277911
seq_region_name: 17
source: dbSNP
start: 73413314
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413316
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1015753204
seq_region_name: 17
source: dbSNP
start: 73413320
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1445357895
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs778543863
seq_region_name: 17
source: dbSNP
start: 73413332
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs974662083
seq_region_name: 17
source: dbSNP
start: 73413350
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413355
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs930708699
seq_region_name: 17
source: dbSNP
start: 73413357
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1158415881
seq_region_name: 17
source: dbSNP
start: 73413359
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413360
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413363
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413369
strand: 1
-
alleles:
- TATA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413372
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1419601082
seq_region_name: 17
source: dbSNP
start: 73413374
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs747727563
seq_region_name: 17
source: dbSNP
start: 73413375
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063155216
seq_region_name: 17
source: dbSNP
start: 73413376
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413387
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063155262
seq_region_name: 17
source: dbSNP
start: 73413388
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413390
feature_type: variation
id: rs1410260014
seq_region_name: 17
source: dbSNP
start: 73413390
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs951891257
seq_region_name: 17
source: dbSNP
start: 73413395
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063155333
seq_region_name: 17
source: dbSNP
start: 73413396
strand: 1
-
alleles:
- GTGATAGT
- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413399
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1555764673
seq_region_name: 17
source: dbSNP
start: 73413401
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413403
feature_type: variation
id: rs1180131820
seq_region_name: 17
source: dbSNP
start: 73413403
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413410
feature_type: variation
id: rs2063155413
seq_region_name: 17
source: dbSNP
start: 73413410
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063155432
seq_region_name: 17
source: dbSNP
start: 73413411
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs980400274
seq_region_name: 17
source: dbSNP
start: 73413414
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413421
feature_type: variation
id: rs577681025
seq_region_name: 17
source: dbSNP
start: 73413421
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413424
feature_type: variation
id: rs926323598
seq_region_name: 17
source: dbSNP
start: 73413424
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413425
feature_type: variation
id: rs984858033
seq_region_name: 17
source: dbSNP
start: 73413425
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413426
feature_type: variation
id: rs1463860501
seq_region_name: 17
source: dbSNP
start: 73413426
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413429
feature_type: variation
id: rs2063155566
seq_region_name: 17
source: dbSNP
start: 73413429
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413435
feature_type: variation
id: rs1473651092
seq_region_name: 17
source: dbSNP
start: 73413434
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413435
feature_type: variation
id: rs367938316
seq_region_name: 17
source: dbSNP
start: 73413435
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413436
feature_type: variation
id: rs2063155636
seq_region_name: 17
source: dbSNP
start: 73413436
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413438
feature_type: variation
id: rs926763396
seq_region_name: 17
source: dbSNP
start: 73413438
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413451
feature_type: variation
id: rs1161447776
seq_region_name: 17
source: dbSNP
start: 73413451
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413452
feature_type: variation
id: rs939256692
seq_region_name: 17
source: dbSNP
start: 73413452
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413456
feature_type: variation
id: rs1226067198
seq_region_name: 17
source: dbSNP
start: 73413456
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413461
feature_type: variation
id: rs1412945274
seq_region_name: 17
source: dbSNP
start: 73413461
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413463
feature_type: variation
id: rs2063155759
seq_region_name: 17
source: dbSNP
start: 73413463
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413464
feature_type: variation
id: rs2063155783
seq_region_name: 17
source: dbSNP
start: 73413464
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413465
feature_type: variation
id: rs1457346723
seq_region_name: 17
source: dbSNP
start: 73413465
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413471
feature_type: variation
id: rs992059469
seq_region_name: 17
source: dbSNP
start: 73413471
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413472
feature_type: variation
id: rs9302964
seq_region_name: 17
source: dbSNP
start: 73413472
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413478
feature_type: variation
id: rs1454236734
seq_region_name: 17
source: dbSNP
start: 73413478
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413480
feature_type: variation
id: rs2063155912
seq_region_name: 17
source: dbSNP
start: 73413480
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413481
feature_type: variation
id: rs1386273998
seq_region_name: 17
source: dbSNP
start: 73413481
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413489
feature_type: variation
id: rs773783522
seq_region_name: 17
source: dbSNP
start: 73413489
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413490
feature_type: variation
id: rs918173763
seq_region_name: 17
source: dbSNP
start: 73413490
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413493
feature_type: variation
id: rs1454263468
seq_region_name: 17
source: dbSNP
start: 73413493
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413496
feature_type: variation
id: rs1346847583
seq_region_name: 17
source: dbSNP
start: 73413496
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413499
feature_type: variation
id: rs945200424
seq_region_name: 17
source: dbSNP
start: 73413499
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413503
feature_type: variation
id: rs1423365172
seq_region_name: 17
source: dbSNP
start: 73413503
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413506
feature_type: variation
id: rs1041365252
seq_region_name: 17
source: dbSNP
start: 73413506
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413510
feature_type: variation
id: rs2063156101
seq_region_name: 17
source: dbSNP
start: 73413510
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413515
feature_type: variation
id: rs2063156127
seq_region_name: 17
source: dbSNP
start: 73413515
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413517
feature_type: variation
id: rs1185718611
seq_region_name: 17
source: dbSNP
start: 73413517
strand: 1
-
alleles:
- AAAAA
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413523
feature_type: variation
id: rs34063971
seq_region_name: 17
source: dbSNP
start: 73413519
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413525
feature_type: variation
id: rs2145565607
seq_region_name: 17
source: dbSNP
start: 73413525
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73413710
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73413716
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73413729
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73413731
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73413752
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413756
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1346002468
seq_region_name: 17
source: dbSNP
start: 73413757
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs769684722
seq_region_name: 17
source: dbSNP
start: 73413759
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063157726
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063157747
seq_region_name: 17
source: dbSNP
start: 73413763
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413764
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413765
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73413766
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413769
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1376288188
seq_region_name: 17
source: dbSNP
start: 73413770
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063157894
seq_region_name: 17
source: dbSNP
start: 73413771
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063157918
seq_region_name: 17
source: dbSNP
start: 73413773
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063157938
seq_region_name: 17
source: dbSNP
start: 73413775
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413780
feature_type: variation
id: rs2063157964
seq_region_name: 17
source: dbSNP
start: 73413780
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413781
feature_type: variation
id: rs144830472
seq_region_name: 17
source: dbSNP
start: 73413781
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413782
feature_type: variation
id: rs2063157990
seq_region_name: 17
source: dbSNP
start: 73413782
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413783
feature_type: variation
id: rs2063158023
seq_region_name: 17
source: dbSNP
start: 73413783
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413789
feature_type: variation
id: rs1432036081
seq_region_name: 17
source: dbSNP
start: 73413789
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413800
feature_type: variation
id: rs2063158061
seq_region_name: 17
source: dbSNP
start: 73413800
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413806
feature_type: variation
id: rs2063158091
seq_region_name: 17
source: dbSNP
start: 73413806
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73413929
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73413931
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413934
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73413938
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413941
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73413942
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73413946
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413947
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063159081
seq_region_name: 17
source: dbSNP
start: 73413951
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1006174833
seq_region_name: 17
source: dbSNP
start: 73413956
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413958
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413959
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73413961
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413962
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413963
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73413965
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73413968
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1483344168
seq_region_name: 17
source: dbSNP
start: 73413969
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1241227964
seq_region_name: 17
source: dbSNP
start: 73413970
strand: 1
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alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs369423815
seq_region_name: 17
source: dbSNP
start: 73413971
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413975
feature_type: variation
id: rs74848164
seq_region_name: 17
source: dbSNP
start: 73413975
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249501573
seq_region_name: 17
source: dbSNP
start: 73413978
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413980
feature_type: variation
id: rs182432346
seq_region_name: 17
source: dbSNP
start: 73413980
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063159415
seq_region_name: 17
source: dbSNP
start: 73413982
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413986
feature_type: variation
id: rs1599542622
seq_region_name: 17
source: dbSNP
start: 73413986
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063159466
seq_region_name: 17
source: dbSNP
start: 73413991
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413995
feature_type: variation
id: rs2063159489
seq_region_name: 17
source: dbSNP
start: 73413995
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73413999
feature_type: variation
id: rs1453641664
seq_region_name: 17
source: dbSNP
start: 73413999
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414001
feature_type: variation
id: rs2063159531
seq_region_name: 17
source: dbSNP
start: 73414001
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414004
feature_type: variation
id: rs2063159559
seq_region_name: 17
source: dbSNP
start: 73414004
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1408840896
seq_region_name: 17
source: dbSNP
start: 73414006
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs918062616
seq_region_name: 17
source: dbSNP
start: 73414007
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414008
feature_type: variation
id: rs1021074238
seq_region_name: 17
source: dbSNP
start: 73414008
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs568332733
seq_region_name: 17
source: dbSNP
start: 73414009
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414011
feature_type: variation
id: rs767297498
seq_region_name: 17
source: dbSNP
start: 73414011
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414012
feature_type: variation
id: rs1382828085
seq_region_name: 17
source: dbSNP
start: 73414012
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414014
feature_type: variation
id: rs187133510
seq_region_name: 17
source: dbSNP
start: 73414014
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414015
feature_type: variation
id: rs2145566565
seq_region_name: 17
source: dbSNP
start: 73414015
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414018
feature_type: variation
id: rs1568390649
seq_region_name: 17
source: dbSNP
start: 73414018
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414023
feature_type: variation
id: rs1444798789
seq_region_name: 17
source: dbSNP
start: 73414023
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414026
feature_type: variation
id: rs1375298309
seq_region_name: 17
source: dbSNP
start: 73414026
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414030
feature_type: variation
id: rs2063159769
seq_region_name: 17
source: dbSNP
start: 73414030
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414032
feature_type: variation
id: rs1599542669
seq_region_name: 17
source: dbSNP
start: 73414032
strand: 1
-
alleles:
- TT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414033
feature_type: variation
id: rs774474792
seq_region_name: 17
source: dbSNP
start: 73414032
strand: 1
-
alleles:
- TCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414035
feature_type: variation
id: rs1244762506
seq_region_name: 17
source: dbSNP
start: 73414033
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414034
feature_type: variation
id: rs2345422
seq_region_name: 17
source: dbSNP
start: 73414034
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414039
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs989799018
seq_region_name: 17
source: dbSNP
start: 73414040
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414040
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063160065
seq_region_name: 17
source: dbSNP
start: 73414040
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1246991061
seq_region_name: 17
source: dbSNP
start: 73414042
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063160113
seq_region_name: 17
source: dbSNP
start: 73414043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414046
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1390922746
seq_region_name: 17
source: dbSNP
start: 73414047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414048
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414049
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs571297220
seq_region_name: 17
source: dbSNP
start: 73414050
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414051
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs767123645
seq_region_name: 17
source: dbSNP
start: 73414052
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs76486596
seq_region_name: 17
source: dbSNP
start: 73414053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs538614438
seq_region_name: 17
source: dbSNP
start: 73414058
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1162316519
seq_region_name: 17
source: dbSNP
start: 73414059
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063160380
seq_region_name: 17
source: dbSNP
start: 73414061
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs192757635
seq_region_name: 17
source: dbSNP
start: 73414063
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568390686
seq_region_name: 17
source: dbSNP
start: 73414064
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs573469715
seq_region_name: 17
source: dbSNP
start: 73414064
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1274473408
seq_region_name: 17
source: dbSNP
start: 73414065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063160520
seq_region_name: 17
source: dbSNP
start: 73414065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1342670781
seq_region_name: 17
source: dbSNP
start: 73414067
strand: 1
-
alleles:
- AGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs901644492
seq_region_name: 17
source: dbSNP
start: 73414070
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063160613
seq_region_name: 17
source: dbSNP
start: 73414071
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063160632
seq_region_name: 17
source: dbSNP
start: 73414072
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs912613970
seq_region_name: 17
source: dbSNP
start: 73414076
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1195328293
seq_region_name: 17
source: dbSNP
start: 73414079
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414080
feature_type: variation
id: rs2063160701
seq_region_name: 17
source: dbSNP
start: 73414080
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145566819
seq_region_name: 17
source: dbSNP
start: 73414085
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs929135776
seq_region_name: 17
source: dbSNP
start: 73414086
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1268284030
seq_region_name: 17
source: dbSNP
start: 73414093
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599542784
seq_region_name: 17
source: dbSNP
start: 73414094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063160784
seq_region_name: 17
source: dbSNP
start: 73414095
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414097
feature_type: variation
id: rs2063160799
seq_region_name: 17
source: dbSNP
start: 73414097
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414101
feature_type: variation
id: rs1223247896
seq_region_name: 17
source: dbSNP
start: 73414101
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414104
feature_type: variation
id: rs1361897209
seq_region_name: 17
source: dbSNP
start: 73414104
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414107
feature_type: variation
id: rs1272802263
seq_region_name: 17
source: dbSNP
start: 73414107
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414110
feature_type: variation
id: rs2145566868
seq_region_name: 17
source: dbSNP
start: 73414110
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414114
feature_type: variation
id: rs2063160879
seq_region_name: 17
source: dbSNP
start: 73414114
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414115
feature_type: variation
id: rs2063160904
seq_region_name: 17
source: dbSNP
start: 73414115
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414116
feature_type: variation
id: rs761846296
seq_region_name: 17
source: dbSNP
start: 73414116
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414116
feature_type: variation
id: rs1209930532
seq_region_name: 17
source: dbSNP
start: 73414116
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414117
feature_type: variation
id: rs534569450
seq_region_name: 17
source: dbSNP
start: 73414117
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414119
feature_type: variation
id: rs1231727090
seq_region_name: 17
source: dbSNP
start: 73414119
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414121
feature_type: variation
id: rs1345384826
seq_region_name: 17
source: dbSNP
start: 73414121
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414123
feature_type: variation
id: rs2063161032
seq_region_name: 17
source: dbSNP
start: 73414123
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414124
feature_type: variation
id: rs1302021911
seq_region_name: 17
source: dbSNP
start: 73414124
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414126
feature_type: variation
id: rs1037025088
seq_region_name: 17
source: dbSNP
start: 73414126
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414128
feature_type: variation
id: rs1599542834
seq_region_name: 17
source: dbSNP
start: 73414128
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414131
feature_type: variation
id: rs2063161133
seq_region_name: 17
source: dbSNP
start: 73414131
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414132
feature_type: variation
id: rs1599542837
seq_region_name: 17
source: dbSNP
start: 73414132
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414133
feature_type: variation
id: rs918609562
seq_region_name: 17
source: dbSNP
start: 73414133
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414134
feature_type: variation
id: rs540878045
seq_region_name: 17
source: dbSNP
start: 73414134
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414138
feature_type: variation
id: rs2063161199
seq_region_name: 17
source: dbSNP
start: 73414138
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414141
feature_type: variation
id: rs2145566976
seq_region_name: 17
source: dbSNP
start: 73414141
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414144
feature_type: variation
id: rs1599542843
seq_region_name: 17
source: dbSNP
start: 73414144
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414147
feature_type: variation
id: rs1450522484
seq_region_name: 17
source: dbSNP
start: 73414147
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414148
feature_type: variation
id: rs1170826985
seq_region_name: 17
source: dbSNP
start: 73414148
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414149
feature_type: variation
id: rs2063161283
seq_region_name: 17
source: dbSNP
start: 73414149
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414151
feature_type: variation
id: rs1409009297
seq_region_name: 17
source: dbSNP
start: 73414151
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414152
feature_type: variation
id: rs1049096946
seq_region_name: 17
source: dbSNP
start: 73414152
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414155
feature_type: variation
id: rs753734316
seq_region_name: 17
source: dbSNP
start: 73414155
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414156
feature_type: variation
id: rs1599542858
seq_region_name: 17
source: dbSNP
start: 73414156
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414157
feature_type: variation
id: rs1388882250
seq_region_name: 17
source: dbSNP
start: 73414157
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414161
feature_type: variation
id: rs554466009
seq_region_name: 17
source: dbSNP
start: 73414161
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414171
feature_type: variation
id: rs2063161449
seq_region_name: 17
source: dbSNP
start: 73414171
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414172
feature_type: variation
id: rs1001623160
seq_region_name: 17
source: dbSNP
start: 73414172
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414173
feature_type: variation
id: rs1200016961
seq_region_name: 17
source: dbSNP
start: 73414173
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414175
feature_type: variation
id: rs895150800
seq_region_name: 17
source: dbSNP
start: 73414175
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414177
feature_type: variation
id: rs1766148603
seq_region_name: 17
source: dbSNP
start: 73414177
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414181
feature_type: variation
id: rs1013636182
seq_region_name: 17
source: dbSNP
start: 73414181
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414185
feature_type: variation
id: rs1204171048
seq_region_name: 17
source: dbSNP
start: 73414185
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414186
feature_type: variation
id: rs1057231873
seq_region_name: 17
source: dbSNP
start: 73414186
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414191
feature_type: variation
id: rs1275580430
seq_region_name: 17
source: dbSNP
start: 73414191
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414192
feature_type: variation
id: rs574143381
seq_region_name: 17
source: dbSNP
start: 73414192
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414193
feature_type: variation
id: rs966857478
seq_region_name: 17
source: dbSNP
start: 73414193
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414195
feature_type: variation
id: rs778766604
seq_region_name: 17
source: dbSNP
start: 73414195
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414196
feature_type: variation
id: rs183592621
seq_region_name: 17
source: dbSNP
start: 73414196
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414198
feature_type: variation
id: rs1441040247
seq_region_name: 17
source: dbSNP
start: 73414197
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414200
feature_type: variation
id: rs2063161718
seq_region_name: 17
source: dbSNP
start: 73414200
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145567148
seq_region_name: 17
source: dbSNP
start: 73414206
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1330669016
seq_region_name: 17
source: dbSNP
start: 73414207
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2881149
seq_region_name: 17
source: dbSNP
start: 73414222
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73414229
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs193224425
seq_region_name: 17
source: dbSNP
start: 73414231
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063161915
seq_region_name: 17
source: dbSNP
start: 73414233
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063161943
seq_region_name: 17
source: dbSNP
start: 73414234
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs902153958
seq_region_name: 17
source: dbSNP
start: 73414238
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1000551435
seq_region_name: 17
source: dbSNP
start: 73414239
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1032228825
seq_region_name: 17
source: dbSNP
start: 73414241
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs544991971
seq_region_name: 17
source: dbSNP
start: 73414248
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599542974
seq_region_name: 17
source: dbSNP
start: 73414253
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162083
seq_region_name: 17
source: dbSNP
start: 73414255
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162111
seq_region_name: 17
source: dbSNP
start: 73414259
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1481373600
seq_region_name: 17
source: dbSNP
start: 73414261
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs985290617
seq_region_name: 17
source: dbSNP
start: 73414268
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162169
seq_region_name: 17
source: dbSNP
start: 73414273
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162195
seq_region_name: 17
source: dbSNP
start: 73414275
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162221
seq_region_name: 17
source: dbSNP
start: 73414276
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162284
seq_region_name: 17
source: dbSNP
start: 73414296
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1019495837
seq_region_name: 17
source: dbSNP
start: 73414297
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162334
seq_region_name: 17
source: dbSNP
start: 73414303
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1176644857
seq_region_name: 17
source: dbSNP
start: 73414305
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1470654084
seq_region_name: 17
source: dbSNP
start: 73414309
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1234854370
seq_region_name: 17
source: dbSNP
start: 73414313
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2042478274
seq_region_name: 17
source: dbSNP
start: 73414316
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063162415
seq_region_name: 17
source: dbSNP
start: 73414317
strand: 1
-
alleles:
- GATTAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162441
seq_region_name: 17
source: dbSNP
start: 73414318
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1353701093
seq_region_name: 17
source: dbSNP
start: 73414319
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1201985670
seq_region_name: 17
source: dbSNP
start: 73414322
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs943039405
seq_region_name: 17
source: dbSNP
start: 73414325
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145567336
seq_region_name: 17
source: dbSNP
start: 73414327
strand: 1
-
alleles:
- TGTGAGCCACTGTG
- TGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414340
feature_type: variation
id: rs2063162532
seq_region_name: 17
source: dbSNP
start: 73414327
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1264142813
seq_region_name: 17
source: dbSNP
start: 73414328
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063162568
seq_region_name: 17
source: dbSNP
start: 73414330
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs975819874
seq_region_name: 17
source: dbSNP
start: 73414334
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs771617682
seq_region_name: 17
source: dbSNP
start: 73414335
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1315596635
seq_region_name: 17
source: dbSNP
start: 73414336
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414336
feature_type: variation
id: rs2063162653
seq_region_name: 17
source: dbSNP
start: 73414336
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414337
feature_type: variation
id: rs923012694
seq_region_name: 17
source: dbSNP
start: 73414337
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414339
feature_type: variation
id: rs2063162707
seq_region_name: 17
source: dbSNP
start: 73414339
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs560072980
seq_region_name: 17
source: dbSNP
start: 73414341
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414342
feature_type: variation
id: rs1222665642
seq_region_name: 17
source: dbSNP
start: 73414342
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414343
feature_type: variation
id: rs929105613
seq_region_name: 17
source: dbSNP
start: 73414343
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs973250581
seq_region_name: 17
source: dbSNP
start: 73414344
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414347
feature_type: variation
id: rs2063162793
seq_region_name: 17
source: dbSNP
start: 73414347
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414349
feature_type: variation
id: rs1449995950
seq_region_name: 17
source: dbSNP
start: 73414349
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414354
feature_type: variation
id: rs918696183
seq_region_name: 17
source: dbSNP
start: 73414354
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414355
feature_type: variation
id: rs2063162860
seq_region_name: 17
source: dbSNP
start: 73414355
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414358
feature_type: variation
id: rs1047541801
seq_region_name: 17
source: dbSNP
start: 73414358
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414368
feature_type: variation
id: rs931276586
seq_region_name: 17
source: dbSNP
start: 73414368
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414374
feature_type: variation
id: rs2063162939
seq_region_name: 17
source: dbSNP
start: 73414374
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414383
feature_type: variation
id: rs887629839
seq_region_name: 17
source: dbSNP
start: 73414383
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414386
feature_type: variation
id: rs2063162967
seq_region_name: 17
source: dbSNP
start: 73414386
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414389
feature_type: variation
id: rs2063162988
seq_region_name: 17
source: dbSNP
start: 73414389
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414390
feature_type: variation
id: rs984145656
seq_region_name: 17
source: dbSNP
start: 73414390
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414393
feature_type: variation
id: rs1599543053
seq_region_name: 17
source: dbSNP
start: 73414393
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414397
feature_type: variation
id: rs927510119
seq_region_name: 17
source: dbSNP
start: 73414397
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414400
feature_type: variation
id: rs2063163080
seq_region_name: 17
source: dbSNP
start: 73414399
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414400
feature_type: variation
id: rs1428286072
seq_region_name: 17
source: dbSNP
start: 73414400
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414402
feature_type: variation
id: rs184722576
seq_region_name: 17
source: dbSNP
start: 73414402
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414405
feature_type: variation
id: rs1166172111
seq_region_name: 17
source: dbSNP
start: 73414405
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414406
feature_type: variation
id: rs937633158
seq_region_name: 17
source: dbSNP
start: 73414406
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414407
feature_type: variation
id: rs1057216602
seq_region_name: 17
source: dbSNP
start: 73414407
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414413
feature_type: variation
id: rs2063163233
seq_region_name: 17
source: dbSNP
start: 73414412
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414418
feature_type: variation
id: rs941922995
seq_region_name: 17
source: dbSNP
start: 73414418
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414419
feature_type: variation
id: rs778103516
seq_region_name: 17
source: dbSNP
start: 73414419
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414421
feature_type: variation
id: rs1444169325
seq_region_name: 17
source: dbSNP
start: 73414421
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414423
feature_type: variation
id: rs2063163281
seq_region_name: 17
source: dbSNP
start: 73414423
strand: 1
-
alleles:
- GTCAGTCAG
- GTCAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414439
feature_type: variation
id: rs1456485685
seq_region_name: 17
source: dbSNP
start: 73414431
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414442
feature_type: variation
id: rs1185756586
seq_region_name: 17
source: dbSNP
start: 73414442
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414445
feature_type: variation
id: rs2063163363
seq_region_name: 17
source: dbSNP
start: 73414445
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414448
feature_type: variation
id: rs1485194887
seq_region_name: 17
source: dbSNP
start: 73414448
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414449
feature_type: variation
id: rs1164242685
seq_region_name: 17
source: dbSNP
start: 73414449
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414451
feature_type: variation
id: rs1299351510
seq_region_name: 17
source: dbSNP
start: 73414451
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414452
feature_type: variation
id: rs1054973718
seq_region_name: 17
source: dbSNP
start: 73414452
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414456
feature_type: variation
id: rs2063163456
seq_region_name: 17
source: dbSNP
start: 73414456
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414458
feature_type: variation
id: rs2063163474
seq_region_name: 17
source: dbSNP
start: 73414458
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414461
feature_type: variation
id: rs1217099004
seq_region_name: 17
source: dbSNP
start: 73414461
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414463
feature_type: variation
id: rs1317048874
seq_region_name: 17
source: dbSNP
start: 73414463
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414470
feature_type: variation
id: rs1287535213
seq_region_name: 17
source: dbSNP
start: 73414470
strand: 1
-
alleles:
- GTAGCCTTGGGGAAGG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414485
feature_type: variation
id: rs2063163585
seq_region_name: 17
source: dbSNP
start: 73414470
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414476
feature_type: variation
id: rs2063163608
seq_region_name: 17
source: dbSNP
start: 73414476
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414478
feature_type: variation
id: rs946255118
seq_region_name: 17
source: dbSNP
start: 73414478
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414481
feature_type: variation
id: rs895107499
seq_region_name: 17
source: dbSNP
start: 73414481
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414486
feature_type: variation
id: rs1315509590
seq_region_name: 17
source: dbSNP
start: 73414486
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414487
feature_type: variation
id: rs2063163713
seq_region_name: 17
source: dbSNP
start: 73414487
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414489
feature_type: variation
id: rs1014000219
seq_region_name: 17
source: dbSNP
start: 73414489
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414490
feature_type: variation
id: rs1361089864
seq_region_name: 17
source: dbSNP
start: 73414490
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414492
feature_type: variation
id: rs112600012
seq_region_name: 17
source: dbSNP
start: 73414492
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414497
feature_type: variation
id: rs1288276918
seq_region_name: 17
source: dbSNP
start: 73414497
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414500
feature_type: variation
id: rs543446628
seq_region_name: 17
source: dbSNP
start: 73414500
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414501
feature_type: variation
id: rs1347047215
seq_region_name: 17
source: dbSNP
start: 73414501
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414503
feature_type: variation
id: rs999632359
seq_region_name: 17
source: dbSNP
start: 73414503
strand: 1
-
alleles:
- TAAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414507
feature_type: variation
id: rs2063163905
seq_region_name: 17
source: dbSNP
start: 73414504
strand: 1
-
alleles:
- AA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414506
feature_type: variation
id: rs1338584848
seq_region_name: 17
source: dbSNP
start: 73414505
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414506
feature_type: variation
id: rs2063163951
seq_region_name: 17
source: dbSNP
start: 73414506
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414507
feature_type: variation
id: rs2063163976
seq_region_name: 17
source: dbSNP
start: 73414507
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414508
feature_type: variation
id: rs1386047211
seq_region_name: 17
source: dbSNP
start: 73414508
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414510
feature_type: variation
id: rs1165668260
seq_region_name: 17
source: dbSNP
start: 73414510
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414512
feature_type: variation
id: rs2063164048
seq_region_name: 17
source: dbSNP
start: 73414512
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414515
feature_type: variation
id: rs2063164071
seq_region_name: 17
source: dbSNP
start: 73414515
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414524
feature_type: variation
id: rs1599543168
seq_region_name: 17
source: dbSNP
start: 73414524
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414526
feature_type: variation
id: rs1427158751
seq_region_name: 17
source: dbSNP
start: 73414526
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414527
feature_type: variation
id: rs902269586
seq_region_name: 17
source: dbSNP
start: 73414527
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414528
feature_type: variation
id: rs1187682882
seq_region_name: 17
source: dbSNP
start: 73414528
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414534
feature_type: variation
id: rs1264722704
seq_region_name: 17
source: dbSNP
start: 73414534
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414538
feature_type: variation
id: rs9894169
seq_region_name: 17
source: dbSNP
start: 73414538
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414542
feature_type: variation
id: rs1000901566
seq_region_name: 17
source: dbSNP
start: 73414542
strand: 1
-
alleles:
- AGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414551
feature_type: variation
id: rs140288684
seq_region_name: 17
source: dbSNP
start: 73414548
strand: 1
-
alleles:
- AGAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414551
feature_type: variation
id: rs1490034965
seq_region_name: 17
source: dbSNP
start: 73414548
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414549
feature_type: variation
id: rs1599543198
seq_region_name: 17
source: dbSNP
start: 73414549
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414550
feature_type: variation
id: rs1032052928
seq_region_name: 17
source: dbSNP
start: 73414550
strand: 1
-
alleles:
- GGGGGG
- GGGGG
- GGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414556
feature_type: variation
id: rs985678056
seq_region_name: 17
source: dbSNP
start: 73414551
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414552
feature_type: variation
id: rs965698017
seq_region_name: 17
source: dbSNP
start: 73414552
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414554
feature_type: variation
id: rs1215103517
seq_region_name: 17
source: dbSNP
start: 73414554
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414556
feature_type: variation
id: rs1342246648
seq_region_name: 17
source: dbSNP
start: 73414556
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414561
feature_type: variation
id: rs2145567795
seq_region_name: 17
source: dbSNP
start: 73414561
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414562
feature_type: variation
id: rs749072319
seq_region_name: 17
source: dbSNP
start: 73414562
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414565
feature_type: variation
id: rs2063164496
seq_region_name: 17
source: dbSNP
start: 73414565
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414583
feature_type: variation
id: rs922991233
seq_region_name: 17
source: dbSNP
start: 73414583
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414588
feature_type: variation
id: rs1006838216
seq_region_name: 17
source: dbSNP
start: 73414588
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414589
feature_type: variation
id: rs2063164566
seq_region_name: 17
source: dbSNP
start: 73414589
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414591
feature_type: variation
id: rs2063164587
seq_region_name: 17
source: dbSNP
start: 73414591
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414592
feature_type: variation
id: rs2063164605
seq_region_name: 17
source: dbSNP
start: 73414592
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414593
feature_type: variation
id: rs1019438606
seq_region_name: 17
source: dbSNP
start: 73414593
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414594
feature_type: variation
id: rs765385884
seq_region_name: 17
source: dbSNP
start: 73414594
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414596
feature_type: variation
id: rs2063164698
seq_region_name: 17
source: dbSNP
start: 73414596
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414607
feature_type: variation
id: rs368450817
seq_region_name: 17
source: dbSNP
start: 73414607
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414610
feature_type: variation
id: rs750561588
seq_region_name: 17
source: dbSNP
start: 73414610
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414611
feature_type: variation
id: rs1310908241
seq_region_name: 17
source: dbSNP
start: 73414611
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414613
feature_type: variation
id: rs763248284
seq_region_name: 17
source: dbSNP
start: 73414613
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414614
feature_type: variation
id: rs1599543266
seq_region_name: 17
source: dbSNP
start: 73414614
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414615
feature_type: variation
id: rs2063164850
seq_region_name: 17
source: dbSNP
start: 73414615
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414620
feature_type: variation
id: rs983176479
seq_region_name: 17
source: dbSNP
start: 73414620
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414621
feature_type: variation
id: rs766583569
seq_region_name: 17
source: dbSNP
start: 73414621
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414625
feature_type: variation
id: rs1260988354
seq_region_name: 17
source: dbSNP
start: 73414625
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414627
feature_type: variation
id: rs965560881
seq_region_name: 17
source: dbSNP
start: 73414627
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414632
feature_type: variation
id: rs1480620292
seq_region_name: 17
source: dbSNP
start: 73414632
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414634
feature_type: variation
id: rs751985232
seq_region_name: 17
source: dbSNP
start: 73414634
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414635
feature_type: variation
id: rs1427006258
seq_region_name: 17
source: dbSNP
start: 73414635
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: splice_donor_region_variant
end: 73414638
feature_type: variation
id: rs202154952
seq_region_name: 17
source: dbSNP
start: 73414638
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73414639
feature_type: variation
id: rs2063165137
seq_region_name: 17
source: dbSNP
start: 73414638
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414649
feature_type: variation
id: rs2145567928
seq_region_name: 17
source: dbSNP
start: 73414649
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414652
feature_type: variation
id: rs1159470030
seq_region_name: 17
source: dbSNP
start: 73414652
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414664
feature_type: variation
id: rs781695457
seq_region_name: 17
source: dbSNP
start: 73414664
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414665
feature_type: variation
id: rs369041008
seq_region_name: 17
source: dbSNP
start: 73414665
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414671
feature_type: variation
id: rs2063165275
seq_region_name: 17
source: dbSNP
start: 73414671
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414672
feature_type: variation
id: rs2063165300
seq_region_name: 17
source: dbSNP
start: 73414672
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414674
feature_type: variation
id: rs755531247
seq_region_name: 17
source: dbSNP
start: 73414674
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414677
feature_type: variation
id: rs1384832053
seq_region_name: 17
source: dbSNP
start: 73414677
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414678
feature_type: variation
id: rs1406144460
seq_region_name: 17
source: dbSNP
start: 73414678
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73414680
feature_type: variation
id: rs143251430
seq_region_name: 17
source: dbSNP
start: 73414680
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414686
feature_type: variation
id: rs200296942
seq_region_name: 17
source: dbSNP
start: 73414686
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414687
feature_type: variation
id: rs2063165517
seq_region_name: 17
source: dbSNP
start: 73414687
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73414688
feature_type: variation
id: rs147112459
seq_region_name: 17
source: dbSNP
start: 73414688
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414689
feature_type: variation
id: rs148179574
seq_region_name: 17
source: dbSNP
start: 73414689
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414691
feature_type: variation
id: rs1318756386
seq_region_name: 17
source: dbSNP
start: 73414691
strand: 1
-
alleles:
- CAGGTGAAGCG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73414703
feature_type: variation
id: rs749377360
seq_region_name: 17
source: dbSNP
start: 73414693
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414695
feature_type: variation
id: rs772100767
seq_region_name: 17
source: dbSNP
start: 73414695
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73414702
feature_type: variation
id: rs142010985
seq_region_name: 17
source: dbSNP
start: 73414702
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414703
feature_type: variation
id: rs746302299
seq_region_name: 17
source: dbSNP
start: 73414703
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414709
feature_type: variation
id: rs1266505166
seq_region_name: 17
source: dbSNP
start: 73414709
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414710
feature_type: variation
id: rs187987614
seq_region_name: 17
source: dbSNP
start: 73414710
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73414711
feature_type: variation
id: rs150499065
seq_region_name: 17
source: dbSNP
start: 73414711
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73414712
feature_type: variation
id: rs2063165816
seq_region_name: 17
source: dbSNP
start: 73414712
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414716
feature_type: variation
id: rs1409749734
seq_region_name: 17
source: dbSNP
start: 73414716
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414717
feature_type: variation
id: rs191247511
seq_region_name: 17
source: dbSNP
start: 73414717
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414718
feature_type: variation
id: rs201669899
seq_region_name: 17
source: dbSNP
start: 73414718
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414728
feature_type: variation
id: rs139471859
seq_region_name: 17
source: dbSNP
start: 73414728
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414729
feature_type: variation
id: rs375995286
seq_region_name: 17
source: dbSNP
start: 73414729
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73414730
feature_type: variation
id: rs141611857
seq_region_name: 17
source: dbSNP
start: 73414730
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414731
feature_type: variation
id: rs1053433876
seq_region_name: 17
source: dbSNP
start: 73414731
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414733
feature_type: variation
id: rs756652190
seq_region_name: 17
source: dbSNP
start: 73414733
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414734
feature_type: variation
id: rs763511096
seq_region_name: 17
source: dbSNP
start: 73414734
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414735
feature_type: variation
id: rs1182905488
seq_region_name: 17
source: dbSNP
start: 73414735
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414737
feature_type: variation
id: rs1250479452
seq_region_name: 17
source: dbSNP
start: 73414737
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414738
feature_type: variation
id: rs1202963754
seq_region_name: 17
source: dbSNP
start: 73414738
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414741
feature_type: variation
id: rs146223986
seq_region_name: 17
source: dbSNP
start: 73414741
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414743
feature_type: variation
id: rs200600787
seq_region_name: 17
source: dbSNP
start: 73414743
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414744
feature_type: variation
id: rs1222334523
seq_region_name: 17
source: dbSNP
start: 73414744
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73414746
feature_type: variation
id: rs1306371741
seq_region_name: 17
source: dbSNP
start: 73414746
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414748
feature_type: variation
id: rs1160724261
seq_region_name: 17
source: dbSNP
start: 73414748
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414750
feature_type: variation
id: rs1360345111
seq_region_name: 17
source: dbSNP
start: 73414750
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: synonymous_variant
end: 73414752
feature_type: variation
id: rs12386051
seq_region_name: 17
source: dbSNP
start: 73414752
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414753
feature_type: variation
id: rs1289521697
seq_region_name: 17
source: dbSNP
start: 73414753
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73414757
feature_type: variation
id: rs1162126911
seq_region_name: 17
source: dbSNP
start: 73414757
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73414762
feature_type: variation
id: rs745543684
seq_region_name: 17
source: dbSNP
start: 73414762
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73414763
feature_type: variation
id: rs183794577
seq_region_name: 17
source: dbSNP
start: 73414763
strand: 1
-
alleles:
- GAGGAG
- GAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73414768
feature_type: variation
id: rs761074800
seq_region_name: 17
source: dbSNP
start: 73414763
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73414765
feature_type: variation
id: rs2063166634
seq_region_name: 17
source: dbSNP
start: 73414765
strand: 1
-
alleles:
- GAGA
- GAGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73414769
feature_type: variation
id: rs1404936424
seq_region_name: 17
source: dbSNP
start: 73414766
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73414767
feature_type: variation
id: rs893940805
seq_region_name: 17
source: dbSNP
start: 73414767
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73414771
feature_type: variation
id: rs780007010
seq_region_name: 17
source: dbSNP
start: 73414771
strand: 1
-
alleles:
- GAGAGA
- GAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73414776
feature_type: variation
id: rs778882596
seq_region_name: 17
source: dbSNP
start: 73414771
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73414773
feature_type: variation
id: rs746854659
seq_region_name: 17
source: dbSNP
start: 73414773
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414778
feature_type: variation
id: rs376364356
seq_region_name: 17
source: dbSNP
start: 73414778
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414779
feature_type: variation
id: rs773150779
seq_region_name: 17
source: dbSNP
start: 73414779
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414782
feature_type: variation
id: rs1445938034
seq_region_name: 17
source: dbSNP
start: 73414782
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414783
feature_type: variation
id: rs1599543526
seq_region_name: 17
source: dbSNP
start: 73414783
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414784
feature_type: variation
id: rs749426696
seq_region_name: 17
source: dbSNP
start: 73414784
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414787
feature_type: variation
id: rs1383953111
seq_region_name: 17
source: dbSNP
start: 73414787
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414789
feature_type: variation
id: rs2063166947
seq_region_name: 17
source: dbSNP
start: 73414789
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414794
feature_type: variation
id: rs770948894
seq_region_name: 17
source: dbSNP
start: 73414794
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414795
feature_type: variation
id: rs1171543450
seq_region_name: 17
source: dbSNP
start: 73414795
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414796
feature_type: variation
id: rs1568391162
seq_region_name: 17
source: dbSNP
start: 73414796
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414797
feature_type: variation
id: rs538047611
seq_region_name: 17
source: dbSNP
start: 73414797
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414804
feature_type: variation
id: rs745691385
seq_region_name: 17
source: dbSNP
start: 73414804
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414804
feature_type: variation
id: rs2063167061
seq_region_name: 17
source: dbSNP
start: 73414804
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414805
feature_type: variation
id: rs1440289061
seq_region_name: 17
source: dbSNP
start: 73414805
strand: 1
-
alleles:
- GT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414806
feature_type: variation
id: rs2063167133
seq_region_name: 17
source: dbSNP
start: 73414805
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414807
feature_type: variation
id: rs557253660
seq_region_name: 17
source: dbSNP
start: 73414807
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414811
feature_type: variation
id: rs1461737164
seq_region_name: 17
source: dbSNP
start: 73414811
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414814
feature_type: variation
id: rs1258227951
seq_region_name: 17
source: dbSNP
start: 73414814
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414817
feature_type: variation
id: rs1018479910
seq_region_name: 17
source: dbSNP
start: 73414817
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414820
feature_type: variation
id: rs1350132221
seq_region_name: 17
source: dbSNP
start: 73414820
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414822
feature_type: variation
id: rs966001208
seq_region_name: 17
source: dbSNP
start: 73414822
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414824
feature_type: variation
id: rs2063167258
seq_region_name: 17
source: dbSNP
start: 73414824
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414825
feature_type: variation
id: rs2063167278
seq_region_name: 17
source: dbSNP
start: 73414825
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414826
feature_type: variation
id: rs2063167301
seq_region_name: 17
source: dbSNP
start: 73414826
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414830
feature_type: variation
id: rs1253143381
seq_region_name: 17
source: dbSNP
start: 73414830
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414834
feature_type: variation
id: rs377698566
seq_region_name: 17
source: dbSNP
start: 73414834
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414835
feature_type: variation
id: rs1180049873
seq_region_name: 17
source: dbSNP
start: 73414835
strand: 1
-
alleles:
- GGGGTGGGGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414847
feature_type: variation
id: rs2063167392
seq_region_name: 17
source: dbSNP
start: 73414838
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414839
feature_type: variation
id: rs1025515982
seq_region_name: 17
source: dbSNP
start: 73414839
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414840
feature_type: variation
id: rs1453894717
seq_region_name: 17
source: dbSNP
start: 73414840
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414842
feature_type: variation
id: rs2145568518
seq_region_name: 17
source: dbSNP
start: 73414842
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414843
feature_type: variation
id: rs2063167467
seq_region_name: 17
source: dbSNP
start: 73414843
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414849
feature_type: variation
id: rs2063167493
seq_region_name: 17
source: dbSNP
start: 73414849
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414850
feature_type: variation
id: rs1342616201
seq_region_name: 17
source: dbSNP
start: 73414850
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414851
feature_type: variation
id: rs1316908386
seq_region_name: 17
source: dbSNP
start: 73414851
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414853
feature_type: variation
id: rs1382150298
seq_region_name: 17
source: dbSNP
start: 73414853
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414858
feature_type: variation
id: rs2063167559
seq_region_name: 17
source: dbSNP
start: 73414858
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414860
feature_type: variation
id: rs2063167581
seq_region_name: 17
source: dbSNP
start: 73414860
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414865
feature_type: variation
id: rs72844105
seq_region_name: 17
source: dbSNP
start: 73414865
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414866
feature_type: variation
id: rs983123533
seq_region_name: 17
source: dbSNP
start: 73414866
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414867
feature_type: variation
id: rs2063167667
seq_region_name: 17
source: dbSNP
start: 73414867
strand: 1
-
alleles:
- CCCCCC
- CCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414872
feature_type: variation
id: rs950394744
seq_region_name: 17
source: dbSNP
start: 73414867
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414870
feature_type: variation
id: rs2063167718
seq_region_name: 17
source: dbSNP
start: 73414870
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414871
feature_type: variation
id: rs2063167749
seq_region_name: 17
source: dbSNP
start: 73414871
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414872
feature_type: variation
id: rs2063167774
seq_region_name: 17
source: dbSNP
start: 73414872
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414872
feature_type: variation
id: rs1382963429
seq_region_name: 17
source: dbSNP
start: 73414873
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414874
feature_type: variation
id: rs1162500196
seq_region_name: 17
source: dbSNP
start: 73414874
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414875
feature_type: variation
id: rs1005615436
seq_region_name: 17
source: dbSNP
start: 73414875
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414876
feature_type: variation
id: rs2063167860
seq_region_name: 17
source: dbSNP
start: 73414876
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414880
feature_type: variation
id: rs1369975349
seq_region_name: 17
source: dbSNP
start: 73414880
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414882
feature_type: variation
id: rs2063167907
seq_region_name: 17
source: dbSNP
start: 73414882
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414883
feature_type: variation
id: rs2063167929
seq_region_name: 17
source: dbSNP
start: 73414883
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414884
feature_type: variation
id: rs908962492
seq_region_name: 17
source: dbSNP
start: 73414884
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414888
feature_type: variation
id: rs2063167976
seq_region_name: 17
source: dbSNP
start: 73414888
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73414889
feature_type: variation
id: rs963130416
seq_region_name: 17
source: dbSNP
start: 73414889
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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end: 73414895
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415058
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415060
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415061
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415063
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415068
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415087
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415090
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415095
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73415095
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73415097
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415098
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415099
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415102
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415109
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73415125
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415126
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415128
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415130
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415132
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415134
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73415135
feature_type: variation
id: rs2063169893
seq_region_name: 17
source: dbSNP
start: 73415135
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415137
feature_type: variation
id: rs1599543878
seq_region_name: 17
source: dbSNP
start: 73415137
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1004495895
seq_region_name: 17
source: dbSNP
start: 73415140
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415141
feature_type: variation
id: rs926218694
seq_region_name: 17
source: dbSNP
start: 73415141
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs957499709
seq_region_name: 17
source: dbSNP
start: 73415143
strand: 1
-
alleles:
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- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs986308368
seq_region_name: 17
source: dbSNP
start: 73415147
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415149
feature_type: variation
id: rs1427669911
seq_region_name: 17
source: dbSNP
start: 73415149
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415151
feature_type: variation
id: rs910935639
seq_region_name: 17
source: dbSNP
start: 73415151
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415153
feature_type: variation
id: rs753672965
seq_region_name: 17
source: dbSNP
start: 73415153
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415156
feature_type: variation
id: rs2063170121
seq_region_name: 17
source: dbSNP
start: 73415156
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415161
feature_type: variation
id: rs2063170145
seq_region_name: 17
source: dbSNP
start: 73415161
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415162
feature_type: variation
id: rs2063170166
seq_region_name: 17
source: dbSNP
start: 73415162
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415163
feature_type: variation
id: rs1041102254
seq_region_name: 17
source: dbSNP
start: 73415163
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415167
feature_type: variation
id: rs2063170216
seq_region_name: 17
source: dbSNP
start: 73415167
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415169
feature_type: variation
id: rs1405211014
seq_region_name: 17
source: dbSNP
start: 73415169
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415171
feature_type: variation
id: rs115245377
seq_region_name: 17
source: dbSNP
start: 73415171
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415173
feature_type: variation
id: rs2063170270
seq_region_name: 17
source: dbSNP
start: 73415173
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs929649344
seq_region_name: 17
source: dbSNP
start: 73415174
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415179
feature_type: variation
id: rs2063170317
seq_region_name: 17
source: dbSNP
start: 73415179
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415181
feature_type: variation
id: rs2063170351
seq_region_name: 17
source: dbSNP
start: 73415180
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415183
feature_type: variation
id: rs1416289361
seq_region_name: 17
source: dbSNP
start: 73415183
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415186
feature_type: variation
id: rs34528142
seq_region_name: 17
source: dbSNP
start: 73415186
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415195
feature_type: variation
id: rs888371214
seq_region_name: 17
source: dbSNP
start: 73415195
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415199
feature_type: variation
id: rs2063170397
seq_region_name: 17
source: dbSNP
start: 73415199
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415204
feature_type: variation
id: rs941157266
seq_region_name: 17
source: dbSNP
start: 73415204
strand: 1
-
alleles:
- AA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415211
feature_type: variation
id: rs2063170441
seq_region_name: 17
source: dbSNP
start: 73415210
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415211
feature_type: variation
id: rs990601160
seq_region_name: 17
source: dbSNP
start: 73415211
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415214
feature_type: variation
id: rs2063170488
seq_region_name: 17
source: dbSNP
start: 73415214
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415219
feature_type: variation
id: rs1599543929
seq_region_name: 17
source: dbSNP
start: 73415219
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415220
feature_type: variation
id: rs1182091547
seq_region_name: 17
source: dbSNP
start: 73415220
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415221
feature_type: variation
id: rs1461125113
seq_region_name: 17
source: dbSNP
start: 73415221
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415222
feature_type: variation
id: rs1023863573
seq_region_name: 17
source: dbSNP
start: 73415222
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415228
feature_type: variation
id: rs1212846970
seq_region_name: 17
source: dbSNP
start: 73415228
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415229
feature_type: variation
id: rs1440651780
seq_region_name: 17
source: dbSNP
start: 73415229
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415235
feature_type: variation
id: rs1055590394
seq_region_name: 17
source: dbSNP
start: 73415235
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415236
feature_type: variation
id: rs982399761
seq_region_name: 17
source: dbSNP
start: 73415236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415237
feature_type: variation
id: rs536222519
seq_region_name: 17
source: dbSNP
start: 73415237
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415240
feature_type: variation
id: rs779414498
seq_region_name: 17
source: dbSNP
start: 73415240
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415244
feature_type: variation
id: rs2063170724
seq_region_name: 17
source: dbSNP
start: 73415244
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415245
feature_type: variation
id: rs2063170745
seq_region_name: 17
source: dbSNP
start: 73415245
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415246
feature_type: variation
id: rs2063170771
seq_region_name: 17
source: dbSNP
start: 73415246
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415249
feature_type: variation
id: rs935270628
seq_region_name: 17
source: dbSNP
start: 73415249
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415250
feature_type: variation
id: rs1450231556
seq_region_name: 17
source: dbSNP
start: 73415250
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415251
feature_type: variation
id: rs2063170838
seq_region_name: 17
source: dbSNP
start: 73415251
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415253
feature_type: variation
id: rs1381739812
seq_region_name: 17
source: dbSNP
start: 73415253
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415254
feature_type: variation
id: rs1014318580
seq_region_name: 17
source: dbSNP
start: 73415254
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415255
feature_type: variation
id: rs1450122461
seq_region_name: 17
source: dbSNP
start: 73415255
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415257
feature_type: variation
id: rs2145569455
seq_region_name: 17
source: dbSNP
start: 73415255
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415262
feature_type: variation
id: rs915269632
seq_region_name: 17
source: dbSNP
start: 73415262
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415280
feature_type: variation
id: rs1272904914
seq_region_name: 17
source: dbSNP
start: 73415280
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415282
feature_type: variation
id: rs1322455665
seq_region_name: 17
source: dbSNP
start: 73415282
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415284
feature_type: variation
id: rs2063171014
seq_region_name: 17
source: dbSNP
start: 73415284
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415285
feature_type: variation
id: rs1223824745
seq_region_name: 17
source: dbSNP
start: 73415285
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415286
feature_type: variation
id: rs2063171053
seq_region_name: 17
source: dbSNP
start: 73415286
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415291
feature_type: variation
id: rs2063171069
seq_region_name: 17
source: dbSNP
start: 73415291
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415293
feature_type: variation
id: rs942755386
seq_region_name: 17
source: dbSNP
start: 73415293
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415303
feature_type: variation
id: rs2063171110
seq_region_name: 17
source: dbSNP
start: 73415303
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415306
feature_type: variation
id: rs1823148108
seq_region_name: 17
source: dbSNP
start: 73415306
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415308
feature_type: variation
id: rs1599544006
seq_region_name: 17
source: dbSNP
start: 73415308
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415309
feature_type: variation
id: rs549459567
seq_region_name: 17
source: dbSNP
start: 73415309
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415313
feature_type: variation
id: rs2063171156
seq_region_name: 17
source: dbSNP
start: 73415313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415322
feature_type: variation
id: rs1039798178
seq_region_name: 17
source: dbSNP
start: 73415322
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415324
feature_type: variation
id: rs1444474814
seq_region_name: 17
source: dbSNP
start: 73415324
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415327
feature_type: variation
id: rs2063171200
seq_region_name: 17
source: dbSNP
start: 73415327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415333
feature_type: variation
id: rs2145569565
seq_region_name: 17
source: dbSNP
start: 73415333
strand: 1
-
alleles:
- TTTT
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415337
feature_type: variation
id: rs901298170
seq_region_name: 17
source: dbSNP
start: 73415334
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415335
feature_type: variation
id: rs1184121048
seq_region_name: 17
source: dbSNP
start: 73415335
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415337
feature_type: variation
id: rs2145569586
seq_region_name: 17
source: dbSNP
start: 73415337
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415339
feature_type: variation
id: rs1965448391
seq_region_name: 17
source: dbSNP
start: 73415339
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415342
feature_type: variation
id: rs2063171266
seq_region_name: 17
source: dbSNP
start: 73415342
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415345
feature_type: variation
id: rs2063171282
seq_region_name: 17
source: dbSNP
start: 73415345
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415346
feature_type: variation
id: rs1485143959
seq_region_name: 17
source: dbSNP
start: 73415346
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415347
feature_type: variation
id: rs1024706610
seq_region_name: 17
source: dbSNP
start: 73415347
strand: 1
-
alleles:
- TCACT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415351
feature_type: variation
id: rs1239880256
seq_region_name: 17
source: dbSNP
start: 73415347
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415348
feature_type: variation
id: rs1488312659
seq_region_name: 17
source: dbSNP
start: 73415348
strand: 1
-
alleles:
- CAC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415350
feature_type: variation
id: rs1215207264
seq_region_name: 17
source: dbSNP
start: 73415348
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415349
feature_type: variation
id: rs1211873464
seq_region_name: 17
source: dbSNP
start: 73415349
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415349
feature_type: variation
id: rs1599544060
seq_region_name: 17
source: dbSNP
start: 73415349
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415350
feature_type: variation
id: rs1260282605
seq_region_name: 17
source: dbSNP
start: 73415350
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415350
feature_type: variation
id: rs1287780467
seq_region_name: 17
source: dbSNP
start: 73415350
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415350
feature_type: variation
id: rs2063171514
seq_region_name: 17
source: dbSNP
start: 73415350
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415351
feature_type: variation
id: rs1188979684
seq_region_name: 17
source: dbSNP
start: 73415351
strand: 1
-
alleles:
- TT
- TTCACTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415352
feature_type: variation
id: rs2063171565
seq_region_name: 17
source: dbSNP
start: 73415351
strand: 1
-
alleles:
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415370
feature_type: variation
id: rs35201251
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249733025
seq_region_name: 17
source: dbSNP
start: 73415352
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063171749
seq_region_name: 17
source: dbSNP
start: 73415360
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1195005993
seq_region_name: 17
source: dbSNP
start: 73415363
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1647749099
seq_region_name: 17
source: dbSNP
start: 73415366
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063171796
seq_region_name: 17
source: dbSNP
start: 73415367
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1477896161
seq_region_name: 17
source: dbSNP
start: 73415369
strand: 1
-
alleles:
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- TTA
- TTGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415370
feature_type: variation
id: rs2063171833
seq_region_name: 17
source: dbSNP
start: 73415371
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1005293862
seq_region_name: 17
source: dbSNP
start: 73415371
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415371
feature_type: variation
id: rs1264702364
seq_region_name: 17
source: dbSNP
start: 73415371
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415372
feature_type: variation
id: rs2063171896
seq_region_name: 17
source: dbSNP
start: 73415372
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1047711266
seq_region_name: 17
source: dbSNP
start: 73415374
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415375
feature_type: variation
id: rs1265844552
seq_region_name: 17
source: dbSNP
start: 73415375
strand: 1
-
alleles:
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- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1406628679
seq_region_name: 17
source: dbSNP
start: 73415376
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1305526308
seq_region_name: 17
source: dbSNP
start: 73415378
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415380
feature_type: variation
id: rs1599544149
seq_region_name: 17
source: dbSNP
start: 73415380
strand: 1
-
alleles:
- TCTC
- TC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415383
feature_type: variation
id: rs1162039959
seq_region_name: 17
source: dbSNP
start: 73415380
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415383
feature_type: variation
id: rs1219161644
seq_region_name: 17
source: dbSNP
start: 73415383
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415385
feature_type: variation
id: rs2145569789
seq_region_name: 17
source: dbSNP
start: 73415385
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415389
feature_type: variation
id: rs1342453444
seq_region_name: 17
source: dbSNP
start: 73415389
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415411
feature_type: variation
id: rs2063172101
seq_region_name: 17
source: dbSNP
start: 73415411
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415412
feature_type: variation
id: rs2063172127
seq_region_name: 17
source: dbSNP
start: 73415412
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415414
feature_type: variation
id: rs2063172150
seq_region_name: 17
source: dbSNP
start: 73415414
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415415
feature_type: variation
id: rs114866961
seq_region_name: 17
source: dbSNP
start: 73415415
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415416
feature_type: variation
id: rs1386448639
seq_region_name: 17
source: dbSNP
start: 73415416
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415417
feature_type: variation
id: rs2063172197
seq_region_name: 17
source: dbSNP
start: 73415417
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415418
feature_type: variation
id: rs2063172213
seq_region_name: 17
source: dbSNP
start: 73415418
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415422
feature_type: variation
id: rs2063172229
seq_region_name: 17
source: dbSNP
start: 73415422
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415423
feature_type: variation
id: rs2063172258
seq_region_name: 17
source: dbSNP
start: 73415423
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415428
feature_type: variation
id: rs999276699
seq_region_name: 17
source: dbSNP
start: 73415428
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415431
feature_type: variation
id: rs1568391496
seq_region_name: 17
source: dbSNP
start: 73415431
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415433
feature_type: variation
id: rs1033232982
seq_region_name: 17
source: dbSNP
start: 73415433
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415434
feature_type: variation
id: rs116650958
seq_region_name: 17
source: dbSNP
start: 73415434
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415438
feature_type: variation
id: rs143388564
seq_region_name: 17
source: dbSNP
start: 73415438
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415440
feature_type: variation
id: rs986297067
seq_region_name: 17
source: dbSNP
start: 73415440
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415442
feature_type: variation
id: rs2145569904
seq_region_name: 17
source: dbSNP
start: 73415442
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415443
feature_type: variation
id: rs1172101354
seq_region_name: 17
source: dbSNP
start: 73415443
strand: 1
-
alleles:
- CCCCA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415447
feature_type: variation
id: rs2063172455
seq_region_name: 17
source: dbSNP
start: 73415443
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415450
feature_type: variation
id: rs1017820818
seq_region_name: 17
source: dbSNP
start: 73415450
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415452
feature_type: variation
id: rs963776761
seq_region_name: 17
source: dbSNP
start: 73415452
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415456
feature_type: variation
id: rs2063172513
seq_region_name: 17
source: dbSNP
start: 73415456
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415459
feature_type: variation
id: rs2063172542
seq_region_name: 17
source: dbSNP
start: 73415459
strand: 1
-
alleles:
- GGGG
- GGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415463
feature_type: variation
id: rs1599544231
seq_region_name: 17
source: dbSNP
start: 73415460
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415461
feature_type: variation
id: rs1196599566
seq_region_name: 17
source: dbSNP
start: 73415461
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415464
feature_type: variation
id: rs1599544238
seq_region_name: 17
source: dbSNP
start: 73415464
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415469
feature_type: variation
id: rs2063172628
seq_region_name: 17
source: dbSNP
start: 73415469
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415470
feature_type: variation
id: rs976551505
seq_region_name: 17
source: dbSNP
start: 73415470
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415471
feature_type: variation
id: rs2063172671
seq_region_name: 17
source: dbSNP
start: 73415471
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415472
feature_type: variation
id: rs2063172686
seq_region_name: 17
source: dbSNP
start: 73415472
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415480
feature_type: variation
id: rs1267672075
seq_region_name: 17
source: dbSNP
start: 73415480
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415481
feature_type: variation
id: rs549555596
seq_region_name: 17
source: dbSNP
start: 73415481
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415490
feature_type: variation
id: rs2063172745
seq_region_name: 17
source: dbSNP
start: 73415490
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415491
feature_type: variation
id: rs2063172765
seq_region_name: 17
source: dbSNP
start: 73415491
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415494
feature_type: variation
id: rs1257113643
seq_region_name: 17
source: dbSNP
start: 73415494
strand: 1
-
alleles:
- TACCACC
- TACCACCTACCACC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415500
feature_type: variation
id: rs970923988
seq_region_name: 17
source: dbSNP
start: 73415494
strand: 1
-
alleles:
- ACCACCAC
- ACCAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415502
feature_type: variation
id: rs2063172851
seq_region_name: 17
source: dbSNP
start: 73415495
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415496
feature_type: variation
id: rs2145570025
seq_region_name: 17
source: dbSNP
start: 73415496
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415499
feature_type: variation
id: rs2063172880
seq_region_name: 17
source: dbSNP
start: 73415499
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415500
feature_type: variation
id: rs1199204891
seq_region_name: 17
source: dbSNP
start: 73415500
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415502
feature_type: variation
id: rs1319856261
seq_region_name: 17
source: dbSNP
start: 73415502
strand: 1
-
alleles:
- CC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415505
feature_type: variation
id: rs1261379441
seq_region_name: 17
source: dbSNP
start: 73415504
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415505
feature_type: variation
id: rs577786874
seq_region_name: 17
source: dbSNP
start: 73415505
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415506
feature_type: variation
id: rs8071252
seq_region_name: 17
source: dbSNP
start: 73415506
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415507
feature_type: variation
id: rs2063173058
seq_region_name: 17
source: dbSNP
start: 73415507
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415516
feature_type: variation
id: rs956591699
seq_region_name: 17
source: dbSNP
start: 73415516
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415520
feature_type: variation
id: rs929624167
seq_region_name: 17
source: dbSNP
start: 73415520
strand: 1
-
alleles:
- TTTTTT
- TTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415527
feature_type: variation
id: rs1271278120
seq_region_name: 17
source: dbSNP
start: 73415522
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415527
feature_type: variation
id: rs1404585063
seq_region_name: 17
source: dbSNP
start: 73415527
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415528
feature_type: variation
id: rs982857386
seq_region_name: 17
source: dbSNP
start: 73415528
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415530
feature_type: variation
id: rs2063173198
seq_region_name: 17
source: dbSNP
start: 73415530
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415535
feature_type: variation
id: rs1465157554
seq_region_name: 17
source: dbSNP
start: 73415535
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415536
feature_type: variation
id: rs373972979
seq_region_name: 17
source: dbSNP
start: 73415536
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415537
feature_type: variation
id: rs1177792804
seq_region_name: 17
source: dbSNP
start: 73415537
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415541
feature_type: variation
id: rs2063173308
seq_region_name: 17
source: dbSNP
start: 73415541
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415545
feature_type: variation
id: rs2063173330
seq_region_name: 17
source: dbSNP
start: 73415545
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415547
feature_type: variation
id: rs942718959
seq_region_name: 17
source: dbSNP
start: 73415547
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415548
feature_type: variation
id: rs1237362636
seq_region_name: 17
source: dbSNP
start: 73415548
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415549
feature_type: variation
id: rs147170499
seq_region_name: 17
source: dbSNP
start: 73415549
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415553
feature_type: variation
id: rs2063173420
seq_region_name: 17
source: dbSNP
start: 73415553
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415566
feature_type: variation
id: rs1055537630
seq_region_name: 17
source: dbSNP
start: 73415566
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415573
feature_type: variation
id: rs2145570184
seq_region_name: 17
source: dbSNP
start: 73415573
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415574
feature_type: variation
id: rs894334831
seq_region_name: 17
source: dbSNP
start: 73415574
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415576
feature_type: variation
id: rs2063173499
seq_region_name: 17
source: dbSNP
start: 73415576
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415577
feature_type: variation
id: rs140358837
seq_region_name: 17
source: dbSNP
start: 73415577
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415578
feature_type: variation
id: rs2063173541
seq_region_name: 17
source: dbSNP
start: 73415578
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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strand: 1
-
alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73415615
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73415634
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73415639
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415654
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415690
strand: 1
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alleles:
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415700
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415703
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415707
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415712
strand: 1
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alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415715
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415716
strand: 1
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alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1283908287
seq_region_name: 17
source: dbSNP
start: 73415719
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415723
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415725
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415728
strand: 1
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alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73415730
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063174735
seq_region_name: 17
source: dbSNP
start: 73415731
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415733
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415733
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415734
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415735
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs976663533
seq_region_name: 17
source: dbSNP
start: 73415736
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1298506654
seq_region_name: 17
source: dbSNP
start: 73415739
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415740
feature_type: variation
id: rs2063174981
seq_region_name: 17
source: dbSNP
start: 73415740
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415741
feature_type: variation
id: rs1421070911
seq_region_name: 17
source: dbSNP
start: 73415741
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415742
feature_type: variation
id: rs181418891
seq_region_name: 17
source: dbSNP
start: 73415742
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1029373693
seq_region_name: 17
source: dbSNP
start: 73415743
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs532333625
seq_region_name: 17
source: dbSNP
start: 73415744
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs868480096
seq_region_name: 17
source: dbSNP
start: 73415749
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs982459414
seq_region_name: 17
source: dbSNP
start: 73415751
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415752
feature_type: variation
id: rs2063175170
seq_region_name: 17
source: dbSNP
start: 73415752
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415755
feature_type: variation
id: rs2063175187
seq_region_name: 17
source: dbSNP
start: 73415755
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415757
feature_type: variation
id: rs2063175206
seq_region_name: 17
source: dbSNP
start: 73415757
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415758
feature_type: variation
id: rs1191398874
seq_region_name: 17
source: dbSNP
start: 73415758
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415762
feature_type: variation
id: rs117886003
seq_region_name: 17
source: dbSNP
start: 73415762
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415764
feature_type: variation
id: rs2063175273
seq_region_name: 17
source: dbSNP
start: 73415764
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415766
feature_type: variation
id: rs759768643
seq_region_name: 17
source: dbSNP
start: 73415766
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415767
feature_type: variation
id: rs1312781690
seq_region_name: 17
source: dbSNP
start: 73415767
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs370831921
seq_region_name: 17
source: dbSNP
start: 73415769
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415771
feature_type: variation
id: rs1289651623
seq_region_name: 17
source: dbSNP
start: 73415771
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415773
feature_type: variation
id: rs1215146072
seq_region_name: 17
source: dbSNP
start: 73415773
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415774
feature_type: variation
id: rs1274850979
seq_region_name: 17
source: dbSNP
start: 73415774
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415777
feature_type: variation
id: rs1305554642
seq_region_name: 17
source: dbSNP
start: 73415777
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415778
feature_type: variation
id: rs529697505
seq_region_name: 17
source: dbSNP
start: 73415778
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415779
feature_type: variation
id: rs374208585
seq_region_name: 17
source: dbSNP
start: 73415779
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415780
feature_type: variation
id: rs1462233346
seq_region_name: 17
source: dbSNP
start: 73415780
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415781
feature_type: variation
id: rs367796635
seq_region_name: 17
source: dbSNP
start: 73415781
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415782
feature_type: variation
id: rs548175913
seq_region_name: 17
source: dbSNP
start: 73415782
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415783
feature_type: variation
id: rs1568391696
seq_region_name: 17
source: dbSNP
start: 73415783
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415784
feature_type: variation
id: rs1314271048
seq_region_name: 17
source: dbSNP
start: 73415784
strand: 1
-
alleles:
- TGGTCTGAGA
- TGGTCTGAGATGGTCTGAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415793
feature_type: variation
id: rs2063175619
seq_region_name: 17
source: dbSNP
start: 73415784
strand: 1
-
alleles:
- TGGTCTGAGACCACA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415798
feature_type: variation
id: rs1278490150
seq_region_name: 17
source: dbSNP
start: 73415784
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415785
feature_type: variation
id: rs1472751181
seq_region_name: 17
source: dbSNP
start: 73415785
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415786
feature_type: variation
id: rs1187688251
seq_region_name: 17
source: dbSNP
start: 73415786
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415793
feature_type: variation
id: rs1599544614
seq_region_name: 17
source: dbSNP
start: 73415793
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415794
feature_type: variation
id: rs1422014353
seq_region_name: 17
source: dbSNP
start: 73415794
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415795
feature_type: variation
id: rs1408588477
seq_region_name: 17
source: dbSNP
start: 73415795
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415797
feature_type: variation
id: rs1170178726
seq_region_name: 17
source: dbSNP
start: 73415797
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73415798
feature_type: variation
id: rs1407153980
seq_region_name: 17
source: dbSNP
start: 73415798
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73415803
feature_type: variation
id: rs2063175876
seq_region_name: 17
source: dbSNP
start: 73415803
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73415804
feature_type: variation
id: rs569503087
seq_region_name: 17
source: dbSNP
start: 73415804
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73415807
feature_type: variation
id: rs949883254
seq_region_name: 17
source: dbSNP
start: 73415807
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73415809
feature_type: variation
id: rs1599544651
seq_region_name: 17
source: dbSNP
start: 73415809
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415811
feature_type: variation
id: rs764713693
seq_region_name: 17
source: dbSNP
start: 73415811
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73415817
feature_type: variation
id: rs2063176029
seq_region_name: 17
source: dbSNP
start: 73415817
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73415818
feature_type: variation
id: rs1334771323
seq_region_name: 17
source: dbSNP
start: 73415818
strand: 1
-
alleles:
- GCG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73415822
feature_type: variation
id: rs775134046
seq_region_name: 17
source: dbSNP
start: 73415820
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415821
feature_type: variation
id: rs1045979492
seq_region_name: 17
source: dbSNP
start: 73415821
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415822
feature_type: variation
id: rs746724792
seq_region_name: 17
source: dbSNP
start: 73415822
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73415829
feature_type: variation
id: rs1271868002
seq_region_name: 17
source: dbSNP
start: 73415829
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415830
feature_type: variation
id: rs370359527
seq_region_name: 17
source: dbSNP
start: 73415830
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73415831
feature_type: variation
id: rs144120477
seq_region_name: 17
source: dbSNP
start: 73415831
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415832
feature_type: variation
id: rs1246399663
seq_region_name: 17
source: dbSNP
start: 73415832
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415833
feature_type: variation
id: rs1263570060
seq_region_name: 17
source: dbSNP
start: 73415833
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415834
feature_type: variation
id: rs1325222012
seq_region_name: 17
source: dbSNP
start: 73415834
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415835
feature_type: variation
id: rs941536543
seq_region_name: 17
source: dbSNP
start: 73415835
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415837
feature_type: variation
id: rs764857320
seq_region_name: 17
source: dbSNP
start: 73415837
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73415841
feature_type: variation
id: rs139142614
seq_region_name: 17
source: dbSNP
start: 73415841
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415843
feature_type: variation
id: rs758126517
seq_region_name: 17
source: dbSNP
start: 73415843
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415844
feature_type: variation
id: rs1217060915
seq_region_name: 17
source: dbSNP
start: 73415844
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415847
feature_type: variation
id: rs2063176424
seq_region_name: 17
source: dbSNP
start: 73415847
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415850
feature_type: variation
id: rs779990477
seq_region_name: 17
source: dbSNP
start: 73415850
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415851
feature_type: variation
id: rs374730545
seq_region_name: 17
source: dbSNP
start: 73415851
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415853
feature_type: variation
id: rs1258179595
seq_region_name: 17
source: dbSNP
start: 73415853
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415858
feature_type: variation
id: rs1193357213
seq_region_name: 17
source: dbSNP
start: 73415858
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415859
feature_type: variation
id: rs2063176565
seq_region_name: 17
source: dbSNP
start: 73415859
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415862
feature_type: variation
id: rs1430500763
seq_region_name: 17
source: dbSNP
start: 73415862
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415863
feature_type: variation
id: rs367853518
seq_region_name: 17
source: dbSNP
start: 73415863
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415864
feature_type: variation
id: rs557475994
seq_region_name: 17
source: dbSNP
start: 73415864
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415866
feature_type: variation
id: rs2063176698
seq_region_name: 17
source: dbSNP
start: 73415866
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415867
feature_type: variation
id: rs1401510429
seq_region_name: 17
source: dbSNP
start: 73415867
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415868
feature_type: variation
id: rs1401377926
seq_region_name: 17
source: dbSNP
start: 73415868
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415869
feature_type: variation
id: rs2067117288
seq_region_name: 17
source: dbSNP
start: 73415869
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415875
feature_type: variation
id: rs770941916
seq_region_name: 17
source: dbSNP
start: 73415875
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415880
feature_type: variation
id: rs1169549853
seq_region_name: 17
source: dbSNP
start: 73415880
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415883
feature_type: variation
id: rs893166688
seq_region_name: 17
source: dbSNP
start: 73415883
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415884
feature_type: variation
id: rs774422994
seq_region_name: 17
source: dbSNP
start: 73415884
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415886
feature_type: variation
id: rs746090993
seq_region_name: 17
source: dbSNP
start: 73415886
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415889
feature_type: variation
id: rs772340490
seq_region_name: 17
source: dbSNP
start: 73415889
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415890
feature_type: variation
id: rs76352587
seq_region_name: 17
source: dbSNP
start: 73415890
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415896
feature_type: variation
id: rs2063177122
seq_region_name: 17
source: dbSNP
start: 73415896
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73415899
feature_type: variation
id: rs761138663
seq_region_name: 17
source: dbSNP
start: 73415899
strand: 1
-
alleles:
- ATGATGA
- ATGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73415909
feature_type: variation
id: rs1445987672
seq_region_name: 17
source: dbSNP
start: 73415903
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415905
feature_type: variation
id: rs1463397786
seq_region_name: 17
source: dbSNP
start: 73415905
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415912
feature_type: variation
id: rs2063177287
seq_region_name: 17
source: dbSNP
start: 73415912
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415916
feature_type: variation
id: rs768931276
seq_region_name: 17
source: dbSNP
start: 73415916
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415919
feature_type: variation
id: rs1331966618
seq_region_name: 17
source: dbSNP
start: 73415919
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415920
feature_type: variation
id: rs2063177387
seq_region_name: 17
source: dbSNP
start: 73415920
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415923
feature_type: variation
id: rs777143185
seq_region_name: 17
source: dbSNP
start: 73415923
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415926
feature_type: variation
id: rs1281574954
seq_region_name: 17
source: dbSNP
start: 73415926
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415929
feature_type: variation
id: rs762236775
seq_region_name: 17
source: dbSNP
start: 73415929
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415930
feature_type: variation
id: rs1216602429
seq_region_name: 17
source: dbSNP
start: 73415930
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415932
feature_type: variation
id: rs764773264
seq_region_name: 17
source: dbSNP
start: 73415932
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415935
feature_type: variation
id: rs1424548432
seq_region_name: 17
source: dbSNP
start: 73415935
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415936
feature_type: variation
id: rs750021124
seq_region_name: 17
source: dbSNP
start: 73415936
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415941
feature_type: variation
id: rs757761833
seq_region_name: 17
source: dbSNP
start: 73415941
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73415942
feature_type: variation
id: rs766182692
seq_region_name: 17
source: dbSNP
start: 73415942
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73415943
feature_type: variation
id: rs751204569
seq_region_name: 17
source: dbSNP
start: 73415943
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415944
feature_type: variation
id: rs754756182
seq_region_name: 17
source: dbSNP
start: 73415944
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415945
feature_type: variation
id: rs538822605
seq_region_name: 17
source: dbSNP
start: 73415945
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415946
feature_type: variation
id: rs1440307753
seq_region_name: 17
source: dbSNP
start: 73415946
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415950
feature_type: variation
id: rs1405961727
seq_region_name: 17
source: dbSNP
start: 73415950
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415952
feature_type: variation
id: rs1419019341
seq_region_name: 17
source: dbSNP
start: 73415952
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415953
feature_type: variation
id: rs1052185832
seq_region_name: 17
source: dbSNP
start: 73415953
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415959
feature_type: variation
id: rs2063177840
seq_region_name: 17
source: dbSNP
start: 73415959
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415960
feature_type: variation
id: rs200098498
seq_region_name: 17
source: dbSNP
start: 73415960
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415964
feature_type: variation
id: rs2063177898
seq_region_name: 17
source: dbSNP
start: 73415964
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415966
feature_type: variation
id: rs2063177933
seq_region_name: 17
source: dbSNP
start: 73415966
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415967
feature_type: variation
id: rs756114873
seq_region_name: 17
source: dbSNP
start: 73415967
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415968
feature_type: variation
id: rs778955063
seq_region_name: 17
source: dbSNP
start: 73415968
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415970
feature_type: variation
id: rs745999186
seq_region_name: 17
source: dbSNP
start: 73415970
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73415971
feature_type: variation
id: rs142227808
seq_region_name: 17
source: dbSNP
start: 73415971
strand: 1
-
alleles:
- GGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73415973
feature_type: variation
id: rs34004346
seq_region_name: 17
source: dbSNP
start: 73415971
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415972
feature_type: variation
id: rs1240806850
seq_region_name: 17
source: dbSNP
start: 73415972
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73415973
feature_type: variation
id: rs2063178127
seq_region_name: 17
source: dbSNP
start: 73415973
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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seq_region_name: 17
source: dbSNP
start: 73415975
strand: 1
-
alleles:
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- C
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assembly_name: GRCh38
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consequence_type: missense_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73415976
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063178279
seq_region_name: 17
source: dbSNP
start: 73415977
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs151029567
seq_region_name: 17
source: dbSNP
start: 73415979
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs149966704
seq_region_name: 17
source: dbSNP
start: 73415980
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063178374
seq_region_name: 17
source: dbSNP
start: 73415983
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063178409
seq_region_name: 17
source: dbSNP
start: 73415985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063178437
seq_region_name: 17
source: dbSNP
start: 73415987
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs2063178465
seq_region_name: 17
source: dbSNP
start: 73415992
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs762404848
seq_region_name: 17
source: dbSNP
start: 73415995
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs770481661
seq_region_name: 17
source: dbSNP
start: 73415997
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs554971858
seq_region_name: 17
source: dbSNP
start: 73415998
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs576473920
seq_region_name: 17
source: dbSNP
start: 73415999
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs1184335404
seq_region_name: 17
source: dbSNP
start: 73416000
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73416003
feature_type: variation
id: rs1236367057
seq_region_name: 17
source: dbSNP
start: 73416003
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs2145571590
seq_region_name: 17
source: dbSNP
start: 73416004
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73416007
feature_type: variation
id: rs377638484
seq_region_name: 17
source: dbSNP
start: 73416007
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs759115745
seq_region_name: 17
source: dbSNP
start: 73416008
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73416009
feature_type: variation
id: rs1599545028
seq_region_name: 17
source: dbSNP
start: 73416009
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416012
feature_type: variation
id: rs767344107
seq_region_name: 17
source: dbSNP
start: 73416012
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs369689883
seq_region_name: 17
source: dbSNP
start: 73416013
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1162411875
seq_region_name: 17
source: dbSNP
start: 73416016
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416018
feature_type: variation
id: rs1397027103
seq_region_name: 17
source: dbSNP
start: 73416018
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416019
feature_type: variation
id: rs1416413376
seq_region_name: 17
source: dbSNP
start: 73416019
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416021
feature_type: variation
id: rs558869616
seq_region_name: 17
source: dbSNP
start: 73416021
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416022
feature_type: variation
id: rs1029632359
seq_region_name: 17
source: dbSNP
start: 73416022
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416023
feature_type: variation
id: rs777731664
seq_region_name: 17
source: dbSNP
start: 73416023
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416024
feature_type: variation
id: rs1807687708
seq_region_name: 17
source: dbSNP
start: 73416024
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416025
feature_type: variation
id: rs753800824
seq_region_name: 17
source: dbSNP
start: 73416025
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416029
feature_type: variation
id: rs758420843
seq_region_name: 17
source: dbSNP
start: 73416029
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416032
feature_type: variation
id: rs2063178939
seq_region_name: 17
source: dbSNP
start: 73416032
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416035
feature_type: variation
id: rs780007687
seq_region_name: 17
source: dbSNP
start: 73416035
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416037
feature_type: variation
id: rs1362190391
seq_region_name: 17
source: dbSNP
start: 73416037
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416039
feature_type: variation
id: rs1265225518
seq_region_name: 17
source: dbSNP
start: 73416039
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416040
feature_type: variation
id: rs760250956
seq_region_name: 17
source: dbSNP
start: 73416039
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416041
feature_type: variation
id: rs747185322
seq_region_name: 17
source: dbSNP
start: 73416041
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1180636591
seq_region_name: 17
source: dbSNP
start: 73416042
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063179112
seq_region_name: 17
source: dbSNP
start: 73416044
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416045
feature_type: variation
id: rs1172105850
seq_region_name: 17
source: dbSNP
start: 73416045
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416046
feature_type: variation
id: rs1568392211
seq_region_name: 17
source: dbSNP
start: 73416046
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416048
feature_type: variation
id: rs2063179202
seq_region_name: 17
source: dbSNP
start: 73416048
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416049
feature_type: variation
id: rs1472727229
seq_region_name: 17
source: dbSNP
start: 73416049
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416050
feature_type: variation
id: rs145070462
seq_region_name: 17
source: dbSNP
start: 73416050
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416051
feature_type: variation
id: rs1568392219
seq_region_name: 17
source: dbSNP
start: 73416051
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416057
feature_type: variation
id: rs1599545108
seq_region_name: 17
source: dbSNP
start: 73416057
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416058
feature_type: variation
id: rs2145571746
seq_region_name: 17
source: dbSNP
start: 73416058
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416059
feature_type: variation
id: rs908633191
seq_region_name: 17
source: dbSNP
start: 73416059
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416061
feature_type: variation
id: rs2063179350
seq_region_name: 17
source: dbSNP
start: 73416061
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416069
feature_type: variation
id: rs1170147174
seq_region_name: 17
source: dbSNP
start: 73416069
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416070
feature_type: variation
id: rs114428428
seq_region_name: 17
source: dbSNP
start: 73416070
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416071
feature_type: variation
id: rs559244330
seq_region_name: 17
source: dbSNP
start: 73416071
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416078
feature_type: variation
id: rs2063179475
seq_region_name: 17
source: dbSNP
start: 73416078
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416080
feature_type: variation
id: rs916088523
seq_region_name: 17
source: dbSNP
start: 73416080
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416085
feature_type: variation
id: rs1311111505
seq_region_name: 17
source: dbSNP
start: 73416085
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416088
feature_type: variation
id: rs529798504
seq_region_name: 17
source: dbSNP
start: 73416088
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416089
feature_type: variation
id: rs1378299970
seq_region_name: 17
source: dbSNP
start: 73416089
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416090
feature_type: variation
id: rs1324504385
seq_region_name: 17
source: dbSNP
start: 73416090
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416092
feature_type: variation
id: rs2145571816
seq_region_name: 17
source: dbSNP
start: 73416092
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416093
feature_type: variation
id: rs2145571824
seq_region_name: 17
source: dbSNP
start: 73416093
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416098
feature_type: variation
id: rs1450356119
seq_region_name: 17
source: dbSNP
start: 73416098
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416099
feature_type: variation
id: rs981292704
seq_region_name: 17
source: dbSNP
start: 73416099
strand: 1
-
alleles:
- GGAAGTG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416105
feature_type: variation
id: rs2063179644
seq_region_name: 17
source: dbSNP
start: 73416099
strand: 1
-
alleles:
- "-"
- ATAATCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416107
feature_type: variation
id: rs2063179665
seq_region_name: 17
source: dbSNP
start: 73416108
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416108
feature_type: variation
id: rs2145571853
seq_region_name: 17
source: dbSNP
start: 73416108
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416109
feature_type: variation
id: rs2063179689
seq_region_name: 17
source: dbSNP
start: 73416109
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416110
feature_type: variation
id: rs1297824983
seq_region_name: 17
source: dbSNP
start: 73416110
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416111
feature_type: variation
id: rs1420474565
seq_region_name: 17
source: dbSNP
start: 73416111
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416112
feature_type: variation
id: rs186844187
seq_region_name: 17
source: dbSNP
start: 73416112
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416113
feature_type: variation
id: rs1362868456
seq_region_name: 17
source: dbSNP
start: 73416113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416114
feature_type: variation
id: rs2063179786
seq_region_name: 17
source: dbSNP
start: 73416114
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416116
feature_type: variation
id: rs1453348761
seq_region_name: 17
source: dbSNP
start: 73416116
strand: 1
-
alleles:
- GTGC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416119
feature_type: variation
id: rs2063179835
seq_region_name: 17
source: dbSNP
start: 73416116
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416119
feature_type: variation
id: rs1438470136
seq_region_name: 17
source: dbSNP
start: 73416119
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416120
feature_type: variation
id: rs2145571915
seq_region_name: 17
source: dbSNP
start: 73416120
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416121
feature_type: variation
id: rs1302332766
seq_region_name: 17
source: dbSNP
start: 73416121
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416122
feature_type: variation
id: rs2063179948
seq_region_name: 17
source: dbSNP
start: 73416122
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416123
feature_type: variation
id: rs2063179983
seq_region_name: 17
source: dbSNP
start: 73416123
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416124
feature_type: variation
id: rs1342601145
seq_region_name: 17
source: dbSNP
start: 73416124
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416125
feature_type: variation
id: rs749545212
seq_region_name: 17
source: dbSNP
start: 73416125
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416127
feature_type: variation
id: rs2145571958
seq_region_name: 17
source: dbSNP
start: 73416127
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416129
feature_type: variation
id: rs1249520155
seq_region_name: 17
source: dbSNP
start: 73416129
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416131
feature_type: variation
id: rs562959932
seq_region_name: 17
source: dbSNP
start: 73416131
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416132
feature_type: variation
id: rs1260326257
seq_region_name: 17
source: dbSNP
start: 73416132
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416133
feature_type: variation
id: rs1209869471
seq_region_name: 17
source: dbSNP
start: 73416133
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416134
feature_type: variation
id: rs1291602353
seq_region_name: 17
source: dbSNP
start: 73416134
strand: 1
-
alleles:
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- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416136
feature_type: variation
id: rs2063180173
seq_region_name: 17
source: dbSNP
start: 73416134
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416136
feature_type: variation
id: rs1054520692
seq_region_name: 17
source: dbSNP
start: 73416136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416137
feature_type: variation
id: rs530409722
seq_region_name: 17
source: dbSNP
start: 73416137
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416138
feature_type: variation
id: rs1192157408
seq_region_name: 17
source: dbSNP
start: 73416138
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416140
feature_type: variation
id: rs943311452
seq_region_name: 17
source: dbSNP
start: 73416140
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416148
feature_type: variation
id: rs1252841246
seq_region_name: 17
source: dbSNP
start: 73416148
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416149
feature_type: variation
id: rs1320868083
seq_region_name: 17
source: dbSNP
start: 73416149
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416151
feature_type: variation
id: rs1290580135
seq_region_name: 17
source: dbSNP
start: 73416151
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416152
feature_type: variation
id: rs1234989083
seq_region_name: 17
source: dbSNP
start: 73416152
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416153
feature_type: variation
id: rs1039093005
seq_region_name: 17
source: dbSNP
start: 73416153
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416153
feature_type: variation
id: rs1338536770
seq_region_name: 17
source: dbSNP
start: 73416153
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416154
feature_type: variation
id: rs1400872211
seq_region_name: 17
source: dbSNP
start: 73416154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416159
feature_type: variation
id: rs2063180459
seq_region_name: 17
source: dbSNP
start: 73416159
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416162
feature_type: variation
id: rs902084788
seq_region_name: 17
source: dbSNP
start: 73416162
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416168
feature_type: variation
id: rs777426872
seq_region_name: 17
source: dbSNP
start: 73416168
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416170
feature_type: variation
id: rs1371816623
seq_region_name: 17
source: dbSNP
start: 73416170
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416171
feature_type: variation
id: rs112795097
seq_region_name: 17
source: dbSNP
start: 73416171
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416172
feature_type: variation
id: rs2063180573
seq_region_name: 17
source: dbSNP
start: 73416172
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416173
feature_type: variation
id: rs2063180599
seq_region_name: 17
source: dbSNP
start: 73416173
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416176
feature_type: variation
id: rs2063180618
seq_region_name: 17
source: dbSNP
start: 73416176
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416177
feature_type: variation
id: rs1047871772
seq_region_name: 17
source: dbSNP
start: 73416177
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416179
feature_type: variation
id: rs886580839
seq_region_name: 17
source: dbSNP
start: 73416179
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416183
feature_type: variation
id: rs938996153
seq_region_name: 17
source: dbSNP
start: 73416183
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416184
feature_type: variation
id: rs1167537705
seq_region_name: 17
source: dbSNP
start: 73416184
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416186
feature_type: variation
id: rs7406414
seq_region_name: 17
source: dbSNP
start: 73416186
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416192
feature_type: variation
id: rs2063180778
seq_region_name: 17
source: dbSNP
start: 73416192
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416197
feature_type: variation
id: rs1189298060
seq_region_name: 17
source: dbSNP
start: 73416197
strand: 1
-
alleles:
- CAA
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416199
feature_type: variation
id: rs1555765406
seq_region_name: 17
source: dbSNP
start: 73416197
strand: 1
-
alleles:
- CAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416199
feature_type: variation
id: rs2063180851
seq_region_name: 17
source: dbSNP
start: 73416197
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416198
feature_type: variation
id: rs1417744161
seq_region_name: 17
source: dbSNP
start: 73416198
strand: 1
-
alleles:
- "-"
- TTTTTTT
- TTTTTTTT
- TTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416198
feature_type: variation
id: rs1163863879
seq_region_name: 17
source: dbSNP
start: 73416199
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416199
feature_type: variation
id: rs1473960845
seq_region_name: 17
source: dbSNP
start: 73416199
strand: 1
-
alleles:
- "-"
- ATTTTTT
- GTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416199
feature_type: variation
id: rs373187962
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416200
feature_type: variation
id: rs868796028
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- T
- TCTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416200
feature_type: variation
id: rs1555765415
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- TTTTTT
- TTTTTTGTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416205
feature_type: variation
id: rs2063180999
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- TTTTTTT
- TTTTTTTATTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416206
feature_type: variation
id: rs2063181019
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- TTTTTTTT
- TTTTTTTTCTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416207
feature_type: variation
id: rs1555765416
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- TTTTTTTTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416214
feature_type: variation
id: rs55713710
seq_region_name: 17
source: dbSNP
start: 73416200
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416201
feature_type: variation
id: rs1173533421
seq_region_name: 17
source: dbSNP
start: 73416201
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416205
feature_type: variation
id: rs1599545338
seq_region_name: 17
source: dbSNP
start: 73416205
strand: 1
-
alleles:
- TTTTTT
- TTTTTTTCTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416214
feature_type: variation
id: rs2063181229
seq_region_name: 17
source: dbSNP
start: 73416209
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416213
feature_type: variation
id: rs74950399
seq_region_name: 17
source: dbSNP
start: 73416213
strand: 1
-
alleles:
- "-"
- TTTTTTTTTAGACGGA
- TTTTTTTTTTA
- TTTTTTTTTTG
- TTTTTTTTTTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416214
feature_type: variation
id: rs2063181270
seq_region_name: 17
source: dbSNP
start: 73416215
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416215
feature_type: variation
id: rs77131455
seq_region_name: 17
source: dbSNP
start: 73416215
strand: 1
-
alleles:
- GAGACG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416220
feature_type: variation
id: rs1432186163
seq_region_name: 17
source: dbSNP
start: 73416215
strand: 1
-
alleles:
- GAGACGGAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416223
feature_type: variation
id: rs2063181351
seq_region_name: 17
source: dbSNP
start: 73416215
strand: 1
-
alleles:
- GAGACGGAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416223
feature_type: variation
id: rs2063181368
seq_region_name: 17
source: dbSNP
start: 73416215
strand: 1
-
alleles:
- GAGACGGAGTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416225
feature_type: variation
id: rs2063181393
seq_region_name: 17
source: dbSNP
start: 73416215
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416216
feature_type: variation
id: rs2063181420
seq_region_name: 17
source: dbSNP
start: 73416216
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416216
feature_type: variation
id: rs2145572307
seq_region_name: 17
source: dbSNP
start: 73416216
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416217
feature_type: variation
id: rs2145572315
seq_region_name: 17
source: dbSNP
start: 73416217
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416219
feature_type: variation
id: rs140534800
seq_region_name: 17
source: dbSNP
start: 73416219
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416220
feature_type: variation
id: rs532635042
seq_region_name: 17
source: dbSNP
start: 73416220
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416222
feature_type: variation
id: rs1383672458
seq_region_name: 17
source: dbSNP
start: 73416222
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416224
feature_type: variation
id: rs1293383981
seq_region_name: 17
source: dbSNP
start: 73416224
strand: 1
-
alleles:
- TCTT
- TCTTCTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416227
feature_type: variation
id: rs2063181553
seq_region_name: 17
source: dbSNP
start: 73416224
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416225
feature_type: variation
id: rs1325732883
seq_region_name: 17
source: dbSNP
start: 73416225
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416227
feature_type: variation
id: rs1199185441
seq_region_name: 17
source: dbSNP
start: 73416227
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416228
feature_type: variation
id: rs1244895142
seq_region_name: 17
source: dbSNP
start: 73416228
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416231
feature_type: variation
id: rs1332030428
seq_region_name: 17
source: dbSNP
start: 73416231
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416234
feature_type: variation
id: rs2063181670
seq_region_name: 17
source: dbSNP
start: 73416234
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416236
feature_type: variation
id: rs1481663168
seq_region_name: 17
source: dbSNP
start: 73416236
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416237
feature_type: variation
id: rs962440936
seq_region_name: 17
source: dbSNP
start: 73416237
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416241
feature_type: variation
id: rs1212750499
seq_region_name: 17
source: dbSNP
start: 73416241
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416246
feature_type: variation
id: rs1232842614
seq_region_name: 17
source: dbSNP
start: 73416246
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416249
feature_type: variation
id: rs547976600
seq_region_name: 17
source: dbSNP
start: 73416249
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416250
feature_type: variation
id: rs566114456
seq_region_name: 17
source: dbSNP
start: 73416250
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416251
feature_type: variation
id: rs2063181818
seq_region_name: 17
source: dbSNP
start: 73416251
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416257
feature_type: variation
id: rs1023089631
seq_region_name: 17
source: dbSNP
start: 73416257
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416258
feature_type: variation
id: rs113354595
seq_region_name: 17
source: dbSNP
start: 73416258
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416259
feature_type: variation
id: rs1260291338
seq_region_name: 17
source: dbSNP
start: 73416259
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416260
feature_type: variation
id: rs2063181916
seq_region_name: 17
source: dbSNP
start: 73416260
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416264
feature_type: variation
id: rs1300525669
seq_region_name: 17
source: dbSNP
start: 73416264
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416265
feature_type: variation
id: rs981790947
seq_region_name: 17
source: dbSNP
start: 73416265
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416266
feature_type: variation
id: rs190082612
seq_region_name: 17
source: dbSNP
start: 73416266
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416268
feature_type: variation
id: rs924570619
seq_region_name: 17
source: dbSNP
start: 73416268
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416270
feature_type: variation
id: rs2063182016
seq_region_name: 17
source: dbSNP
start: 73416270
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416271
feature_type: variation
id: rs2063182041
seq_region_name: 17
source: dbSNP
start: 73416271
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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-
alleles:
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-
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416308
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73416318
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs974727273
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start: 73416327
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs891083949
seq_region_name: 17
source: dbSNP
start: 73416330
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416331
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416337
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1004164498
seq_region_name: 17
source: dbSNP
start: 73416338
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182456
seq_region_name: 17
source: dbSNP
start: 73416342
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416344
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182502
seq_region_name: 17
source: dbSNP
start: 73416346
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416349
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1282807978
seq_region_name: 17
source: dbSNP
start: 73416350
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416352
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1015578561
seq_region_name: 17
source: dbSNP
start: 73416355
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182588
seq_region_name: 17
source: dbSNP
start: 73416357
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416360
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182633
seq_region_name: 17
source: dbSNP
start: 73416363
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416365
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416369
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416372
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182718
seq_region_name: 17
source: dbSNP
start: 73416375
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599545506
seq_region_name: 17
source: dbSNP
start: 73416377
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063182761
seq_region_name: 17
source: dbSNP
start: 73416377
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599545513
seq_region_name: 17
source: dbSNP
start: 73416378
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416383
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs774297035
seq_region_name: 17
source: dbSNP
start: 73416384
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416385
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568392500
seq_region_name: 17
source: dbSNP
start: 73416387
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182916
seq_region_name: 17
source: dbSNP
start: 73416388
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182933
seq_region_name: 17
source: dbSNP
start: 73416390
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs768808683
seq_region_name: 17
source: dbSNP
start: 73416394
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416395
feature_type: variation
id: rs2063182976
seq_region_name: 17
source: dbSNP
start: 73416395
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063182990
seq_region_name: 17
source: dbSNP
start: 73416397
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416398
feature_type: variation
id: rs1310385868
seq_region_name: 17
source: dbSNP
start: 73416398
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416399
feature_type: variation
id: rs2063183037
seq_region_name: 17
source: dbSNP
start: 73416399
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416402
feature_type: variation
id: rs1241843482
seq_region_name: 17
source: dbSNP
start: 73416402
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416405
feature_type: variation
id: rs2063183073
seq_region_name: 17
source: dbSNP
start: 73416405
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416406
feature_type: variation
id: rs1599545538
seq_region_name: 17
source: dbSNP
start: 73416406
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs774458225
seq_region_name: 17
source: dbSNP
start: 73416412
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416416
feature_type: variation
id: rs962752124
seq_region_name: 17
source: dbSNP
start: 73416416
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416417
feature_type: variation
id: rs145622151
seq_region_name: 17
source: dbSNP
start: 73416417
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416422
feature_type: variation
id: rs2063183169
seq_region_name: 17
source: dbSNP
start: 73416422
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416425
feature_type: variation
id: rs1355532384
seq_region_name: 17
source: dbSNP
start: 73416425
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416428
feature_type: variation
id: rs1314332464
seq_region_name: 17
source: dbSNP
start: 73416428
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416429
feature_type: variation
id: rs2063183244
seq_region_name: 17
source: dbSNP
start: 73416429
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416430
feature_type: variation
id: rs1023106515
seq_region_name: 17
source: dbSNP
start: 73416430
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416436
feature_type: variation
id: rs970638615
seq_region_name: 17
source: dbSNP
start: 73416436
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416438
feature_type: variation
id: rs1359691708
seq_region_name: 17
source: dbSNP
start: 73416438
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416443
feature_type: variation
id: rs1158893549
seq_region_name: 17
source: dbSNP
start: 73416443
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416450
feature_type: variation
id: rs2063183327
seq_region_name: 17
source: dbSNP
start: 73416450
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416451
feature_type: variation
id: rs2145572851
seq_region_name: 17
source: dbSNP
start: 73416451
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416455
feature_type: variation
id: rs2063183347
seq_region_name: 17
source: dbSNP
start: 73416455
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416458
feature_type: variation
id: rs2063183365
seq_region_name: 17
source: dbSNP
start: 73416458
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416460
feature_type: variation
id: rs554427530
seq_region_name: 17
source: dbSNP
start: 73416460
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416461
feature_type: variation
id: rs2063183419
seq_region_name: 17
source: dbSNP
start: 73416461
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416472
feature_type: variation
id: rs1048414595
seq_region_name: 17
source: dbSNP
start: 73416472
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416477
feature_type: variation
id: rs2063183470
seq_region_name: 17
source: dbSNP
start: 73416477
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416478
feature_type: variation
id: rs1599545592
seq_region_name: 17
source: dbSNP
start: 73416478
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416482
feature_type: variation
id: rs1186735433
seq_region_name: 17
source: dbSNP
start: 73416482
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416483
feature_type: variation
id: rs2063183537
seq_region_name: 17
source: dbSNP
start: 73416483
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416488
feature_type: variation
id: rs1599545604
seq_region_name: 17
source: dbSNP
start: 73416488
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416494
feature_type: variation
id: rs1424541416
seq_region_name: 17
source: dbSNP
start: 73416494
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416497
feature_type: variation
id: rs766362366
seq_region_name: 17
source: dbSNP
start: 73416497
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416498
feature_type: variation
id: rs2063183610
seq_region_name: 17
source: dbSNP
start: 73416498
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416500
feature_type: variation
id: rs181782009
seq_region_name: 17
source: dbSNP
start: 73416500
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416508
feature_type: variation
id: rs1488062368
seq_region_name: 17
source: dbSNP
start: 73416508
strand: 1
-
alleles:
- TTTGTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416517
feature_type: variation
id: rs2063183661
seq_region_name: 17
source: dbSNP
start: 73416511
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416517
feature_type: variation
id: rs1286970892
seq_region_name: 17
source: dbSNP
start: 73416517
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416518
feature_type: variation
id: rs2063183696
seq_region_name: 17
source: dbSNP
start: 73416518
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416519
feature_type: variation
id: rs1207310720
seq_region_name: 17
source: dbSNP
start: 73416519
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416520
feature_type: variation
id: rs928873330
seq_region_name: 17
source: dbSNP
start: 73416520
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416530
feature_type: variation
id: rs1688991030
seq_region_name: 17
source: dbSNP
start: 73416530
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416535
feature_type: variation
id: rs1265434433
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063183795
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs934927856
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs11077681
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145573071
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1264243000
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- TTATTTTATTTTATTTT
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416589
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416595
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416618
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416625
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1421032180
seq_region_name: 17
source: dbSNP
start: 73416633
strand: 1
-
alleles:
- GG
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416634
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs765147650
seq_region_name: 17
source: dbSNP
start: 73416636
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416636
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416638
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416645
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs752487207
seq_region_name: 17
source: dbSNP
start: 73416646
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416647
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs898244237
seq_region_name: 17
source: dbSNP
start: 73416648
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs891031050
seq_region_name: 17
source: dbSNP
start: 73416651
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1012651295
seq_region_name: 17
source: dbSNP
start: 73416653
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1329149771
seq_region_name: 17
source: dbSNP
start: 73416655
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416661
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1322601465
seq_region_name: 17
source: dbSNP
start: 73416664
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063185029
seq_region_name: 17
source: dbSNP
start: 73416665
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1022612426
seq_region_name: 17
source: dbSNP
start: 73416667
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1004110704
seq_region_name: 17
source: dbSNP
start: 73416672
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599545761
seq_region_name: 17
source: dbSNP
start: 73416676
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1329209506
seq_region_name: 17
source: dbSNP
start: 73416677
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs906840186
seq_region_name: 17
source: dbSNP
start: 73416678
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063185160
seq_region_name: 17
source: dbSNP
start: 73416680
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063185196
seq_region_name: 17
source: dbSNP
start: 73416681
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1466344812
seq_region_name: 17
source: dbSNP
start: 73416681
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1420228235
seq_region_name: 17
source: dbSNP
start: 73416683
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063185265
seq_region_name: 17
source: dbSNP
start: 73416684
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1169881654
seq_region_name: 17
source: dbSNP
start: 73416691
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063185311
seq_region_name: 17
source: dbSNP
start: 73416694
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063185330
seq_region_name: 17
source: dbSNP
start: 73416696
strand: 1
-
alleles:
- CTCCT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416701
feature_type: variation
id: rs1015526149
seq_region_name: 17
source: dbSNP
start: 73416697
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416699
feature_type: variation
id: rs898515880
seq_region_name: 17
source: dbSNP
start: 73416699
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416709
feature_type: variation
id: rs1194700751
seq_region_name: 17
source: dbSNP
start: 73416709
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416716
feature_type: variation
id: rs2063185446
seq_region_name: 17
source: dbSNP
start: 73416716
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416720
feature_type: variation
id: rs995571078
seq_region_name: 17
source: dbSNP
start: 73416720
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416721
feature_type: variation
id: rs2063185490
seq_region_name: 17
source: dbSNP
start: 73416721
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416722
feature_type: variation
id: rs2145573430
seq_region_name: 17
source: dbSNP
start: 73416722
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416728
feature_type: variation
id: rs1308055601
seq_region_name: 17
source: dbSNP
start: 73416728
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416728
feature_type: variation
id: rs1413655904
seq_region_name: 17
source: dbSNP
start: 73416728
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416730
feature_type: variation
id: rs1456934500
seq_region_name: 17
source: dbSNP
start: 73416730
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416736
feature_type: variation
id: rs1375080302
seq_region_name: 17
source: dbSNP
start: 73416736
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416738
feature_type: variation
id: rs1002556648
seq_region_name: 17
source: dbSNP
start: 73416738
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416739
feature_type: variation
id: rs557029216
seq_region_name: 17
source: dbSNP
start: 73416739
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416743
feature_type: variation
id: rs1234823832
seq_region_name: 17
source: dbSNP
start: 73416743
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416745
feature_type: variation
id: rs2063185711
seq_region_name: 17
source: dbSNP
start: 73416745
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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-
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73416871
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73416883
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416888
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416889
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416892
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416893
strand: 1
-
alleles:
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- TAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063186985
seq_region_name: 17
source: dbSNP
start: 73416900
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416901
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416901
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416906
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73416907
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs946366352
seq_region_name: 17
source: dbSNP
start: 73416908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063187081
seq_region_name: 17
source: dbSNP
start: 73416909
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs979158659
seq_region_name: 17
source: dbSNP
start: 73416911
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1393211722
seq_region_name: 17
source: dbSNP
start: 73416913
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416915
feature_type: variation
id: rs1433951510
seq_region_name: 17
source: dbSNP
start: 73416915
strand: 1
-
alleles:
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- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416922
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416918
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416920
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416920
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1760071427
seq_region_name: 17
source: dbSNP
start: 73416923
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416924
feature_type: variation
id: rs2063187248
seq_region_name: 17
source: dbSNP
start: 73416924
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416925
feature_type: variation
id: rs182180334
seq_region_name: 17
source: dbSNP
start: 73416925
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416927
feature_type: variation
id: rs932448251
seq_region_name: 17
source: dbSNP
start: 73416927
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416928
feature_type: variation
id: rs2063187432
seq_region_name: 17
source: dbSNP
start: 73416928
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416934
feature_type: variation
id: rs1401627248
seq_region_name: 17
source: dbSNP
start: 73416934
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416938
feature_type: variation
id: rs577180400
seq_region_name: 17
source: dbSNP
start: 73416938
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416955
feature_type: variation
id: rs186083947
seq_region_name: 17
source: dbSNP
start: 73416955
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416956
feature_type: variation
id: rs141274140
seq_region_name: 17
source: dbSNP
start: 73416956
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416959
feature_type: variation
id: rs1471526311
seq_region_name: 17
source: dbSNP
start: 73416956
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416960
feature_type: variation
id: rs2063187583
seq_region_name: 17
source: dbSNP
start: 73416960
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416968
feature_type: variation
id: rs1188241283
seq_region_name: 17
source: dbSNP
start: 73416968
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416969
feature_type: variation
id: rs1599546032
seq_region_name: 17
source: dbSNP
start: 73416969
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416970
feature_type: variation
id: rs2063187644
seq_region_name: 17
source: dbSNP
start: 73416969
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416970
feature_type: variation
id: rs2063187677
seq_region_name: 17
source: dbSNP
start: 73416970
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73416971
feature_type: variation
id: rs2145573950
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145573973
seq_region_name: 17
source: dbSNP
start: 73416981
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1599546044
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start: 73416983
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73416984
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs375666308
seq_region_name: 17
source: dbSNP
start: 73416985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063187783
seq_region_name: 17
source: dbSNP
start: 73416988
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73416989
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063187825
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145574008
seq_region_name: 17
source: dbSNP
start: 73416996
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063187847
seq_region_name: 17
source: dbSNP
start: 73416997
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs939912759
seq_region_name: 17
source: dbSNP
start: 73417000
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs539851884
seq_region_name: 17
source: dbSNP
start: 73417002
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417003
strand: 1
-
alleles:
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- ATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1442113487
seq_region_name: 17
source: dbSNP
start: 73417005
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417008
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1044510241
seq_region_name: 17
source: dbSNP
start: 73417011
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1305995328
seq_region_name: 17
source: dbSNP
start: 73417014
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs368360501
seq_region_name: 17
source: dbSNP
start: 73417020
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs550879091
seq_region_name: 17
source: dbSNP
start: 73417020
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs545945793
seq_region_name: 17
source: dbSNP
start: 73417022
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599546085
seq_region_name: 17
source: dbSNP
start: 73417025
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs112437418
seq_region_name: 17
source: dbSNP
start: 73417028
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417029
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417030
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1044430004
seq_region_name: 17
source: dbSNP
start: 73417032
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1309381552
seq_region_name: 17
source: dbSNP
start: 73417034
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs148359242
seq_region_name: 17
source: dbSNP
start: 73417038
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs570154583
seq_region_name: 17
source: dbSNP
start: 73417039
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs537503421
seq_region_name: 17
source: dbSNP
start: 73417041
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1165060243
seq_region_name: 17
source: dbSNP
start: 73417043
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs552609499
seq_region_name: 17
source: dbSNP
start: 73417044
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417047
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1469031328
seq_region_name: 17
source: dbSNP
start: 73417048
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417051
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145574158
seq_region_name: 17
source: dbSNP
start: 73417056
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417058
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417060
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1243578208
seq_region_name: 17
source: dbSNP
start: 73417063
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1250979996
seq_region_name: 17
source: dbSNP
start: 73417066
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1219314137
seq_region_name: 17
source: dbSNP
start: 73417068
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417073
feature_type: variation
id: rs1002977481
seq_region_name: 17
source: dbSNP
start: 73417073
strand: 1
-
alleles:
- TATTAGTATT
- TATT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417085
feature_type: variation
id: rs1835817563
seq_region_name: 17
source: dbSNP
start: 73417076
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1273707159
seq_region_name: 17
source: dbSNP
start: 73417080
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599546155
seq_region_name: 17
source: dbSNP
start: 73417081
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417082
feature_type: variation
id: rs1235275603
seq_region_name: 17
source: dbSNP
start: 73417082
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417088
feature_type: variation
id: rs964510396
seq_region_name: 17
source: dbSNP
start: 73417088
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1453562810
seq_region_name: 17
source: dbSNP
start: 73417095
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417098
feature_type: variation
id: rs1295126635
seq_region_name: 17
source: dbSNP
start: 73417098
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417099
feature_type: variation
id: rs1215321966
seq_region_name: 17
source: dbSNP
start: 73417099
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417100
feature_type: variation
id: rs2063188998
seq_region_name: 17
source: dbSNP
start: 73417100
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417101
feature_type: variation
id: rs191282003
seq_region_name: 17
source: dbSNP
start: 73417101
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417109
feature_type: variation
id: rs1568392945
seq_region_name: 17
source: dbSNP
start: 73417109
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417110
feature_type: variation
id: rs1292107152
seq_region_name: 17
source: dbSNP
start: 73417110
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417111
feature_type: variation
id: rs974608970
seq_region_name: 17
source: dbSNP
start: 73417111
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417113
feature_type: variation
id: rs1030791151
seq_region_name: 17
source: dbSNP
start: 73417113
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417124
feature_type: variation
id: rs954858751
seq_region_name: 17
source: dbSNP
start: 73417124
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417125
feature_type: variation
id: rs1350110600
seq_region_name: 17
source: dbSNP
start: 73417125
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417126
feature_type: variation
id: rs983852062
seq_region_name: 17
source: dbSNP
start: 73417126
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417128
feature_type: variation
id: rs2063189282
seq_region_name: 17
source: dbSNP
start: 73417128
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417131
feature_type: variation
id: rs2063189303
seq_region_name: 17
source: dbSNP
start: 73417131
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417132
feature_type: variation
id: rs1169330393
seq_region_name: 17
source: dbSNP
start: 73417132
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417136
feature_type: variation
id: rs2063189354
seq_region_name: 17
source: dbSNP
start: 73417136
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417139
feature_type: variation
id: rs561299137
seq_region_name: 17
source: dbSNP
start: 73417139
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417140
feature_type: variation
id: rs1462746936
seq_region_name: 17
source: dbSNP
start: 73417140
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417143
feature_type: variation
id: rs1477326628
seq_region_name: 17
source: dbSNP
start: 73417143
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417147
feature_type: variation
id: rs2050805708
seq_region_name: 17
source: dbSNP
start: 73417147
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417155
feature_type: variation
id: rs2063189452
seq_region_name: 17
source: dbSNP
start: 73417155
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417162
feature_type: variation
id: rs2063189476
seq_region_name: 17
source: dbSNP
start: 73417162
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417163
feature_type: variation
id: rs1599546211
seq_region_name: 17
source: dbSNP
start: 73417163
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417167
feature_type: variation
id: rs963581496
seq_region_name: 17
source: dbSNP
start: 73417167
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417168
feature_type: variation
id: rs1323458800
seq_region_name: 17
source: dbSNP
start: 73417168
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417170
feature_type: variation
id: rs112310034
seq_region_name: 17
source: dbSNP
start: 73417170
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417173
feature_type: variation
id: rs2063189587
seq_region_name: 17
source: dbSNP
start: 73417173
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417175
feature_type: variation
id: rs1215411894
seq_region_name: 17
source: dbSNP
start: 73417175
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417177
feature_type: variation
id: rs1440594931
seq_region_name: 17
source: dbSNP
start: 73417177
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417178
feature_type: variation
id: rs1599546238
seq_region_name: 17
source: dbSNP
start: 73417178
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417181
feature_type: variation
id: rs1271319214
seq_region_name: 17
source: dbSNP
start: 73417181
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417184
feature_type: variation
id: rs2063189710
seq_region_name: 17
source: dbSNP
start: 73417184
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417185
feature_type: variation
id: rs2063189735
seq_region_name: 17
source: dbSNP
start: 73417185
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417193
feature_type: variation
id: rs916844835
seq_region_name: 17
source: dbSNP
start: 73417193
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417199
feature_type: variation
id: rs1599546243
seq_region_name: 17
source: dbSNP
start: 73417199
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417201
feature_type: variation
id: rs1364642490
seq_region_name: 17
source: dbSNP
start: 73417201
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417202
feature_type: variation
id: rs948190336
seq_region_name: 17
source: dbSNP
start: 73417202
strand: 1
-
alleles:
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- CTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1299436307
seq_region_name: 17
source: dbSNP
start: 73417206
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568392997
seq_region_name: 17
source: dbSNP
start: 73417207
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1294865570
seq_region_name: 17
source: dbSNP
start: 73417208
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063189894
seq_region_name: 17
source: dbSNP
start: 73417210
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1234096409
seq_region_name: 17
source: dbSNP
start: 73417210
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1372178099
seq_region_name: 17
source: dbSNP
start: 73417215
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063189966
seq_region_name: 17
source: dbSNP
start: 73417218
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1306275718
seq_region_name: 17
source: dbSNP
start: 73417222
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1445138072
seq_region_name: 17
source: dbSNP
start: 73417224
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1335543455
seq_region_name: 17
source: dbSNP
start: 73417228
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs969034145
seq_region_name: 17
source: dbSNP
start: 73417234
strand: 1
-
alleles:
- TCTCT
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190095
seq_region_name: 17
source: dbSNP
start: 73417234
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1271472926
seq_region_name: 17
source: dbSNP
start: 73417235
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417238
feature_type: variation
id: rs2063190140
seq_region_name: 17
source: dbSNP
start: 73417238
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190159
seq_region_name: 17
source: dbSNP
start: 73417240
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190188
seq_region_name: 17
source: dbSNP
start: 73417240
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1467893595
seq_region_name: 17
source: dbSNP
start: 73417241
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1355969255
seq_region_name: 17
source: dbSNP
start: 73417241
strand: 1
-
alleles:
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAA
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- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417256
feature_type: variation
id: rs112364858
seq_region_name: 17
source: dbSNP
start: 73417242
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1785219216
seq_region_name: 17
source: dbSNP
start: 73417246
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1243790012
seq_region_name: 17
source: dbSNP
start: 73417249
strand: 1
-
alleles:
- "-"
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190295
seq_region_name: 17
source: dbSNP
start: 73417254
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417254
feature_type: variation
id: rs2063190323
seq_region_name: 17
source: dbSNP
start: 73417254
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs868087720
seq_region_name: 17
source: dbSNP
start: 73417257
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs920965485
seq_region_name: 17
source: dbSNP
start: 73417261
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1046561675
seq_region_name: 17
source: dbSNP
start: 73417262
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1418018999
seq_region_name: 17
source: dbSNP
start: 73417263
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1349064407
seq_region_name: 17
source: dbSNP
start: 73417264
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599546335
seq_region_name: 17
source: dbSNP
start: 73417266
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1282858515
seq_region_name: 17
source: dbSNP
start: 73417267
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599546341
seq_region_name: 17
source: dbSNP
start: 73417268
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs943478764
seq_region_name: 17
source: dbSNP
start: 73417271
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417273
feature_type: variation
id: rs1475887835
seq_region_name: 17
source: dbSNP
start: 73417273
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190547
seq_region_name: 17
source: dbSNP
start: 73417281
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190567
seq_region_name: 17
source: dbSNP
start: 73417286
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs953907529
seq_region_name: 17
source: dbSNP
start: 73417293
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417298
feature_type: variation
id: rs928365139
seq_region_name: 17
source: dbSNP
start: 73417298
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063190657
seq_region_name: 17
source: dbSNP
start: 73417299
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs912361330
seq_region_name: 17
source: dbSNP
start: 73417304
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417305
feature_type: variation
id: rs1393228664
seq_region_name: 17
source: dbSNP
start: 73417305
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417309
feature_type: variation
id: rs2063190718
seq_region_name: 17
source: dbSNP
start: 73417309
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417310
feature_type: variation
id: rs574601795
seq_region_name: 17
source: dbSNP
start: 73417310
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417312
feature_type: variation
id: rs1461273404
seq_region_name: 17
source: dbSNP
start: 73417312
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417327
feature_type: variation
id: rs938474263
seq_region_name: 17
source: dbSNP
start: 73417327
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417328
feature_type: variation
id: rs2063190787
seq_region_name: 17
source: dbSNP
start: 73417328
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417330
feature_type: variation
id: rs2145574604
seq_region_name: 17
source: dbSNP
start: 73417330
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417332
feature_type: variation
id: rs2063190812
seq_region_name: 17
source: dbSNP
start: 73417332
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417335
feature_type: variation
id: rs1319328864
seq_region_name: 17
source: dbSNP
start: 73417335
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417336
feature_type: variation
id: rs1175325918
seq_region_name: 17
source: dbSNP
start: 73417336
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417337
feature_type: variation
id: rs1417606925
seq_region_name: 17
source: dbSNP
start: 73417337
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417341
feature_type: variation
id: rs2063190895
seq_region_name: 17
source: dbSNP
start: 73417341
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417343
feature_type: variation
id: rs1599546394
seq_region_name: 17
source: dbSNP
start: 73417343
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417345
feature_type: variation
id: rs939861462
seq_region_name: 17
source: dbSNP
start: 73417345
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417346
feature_type: variation
id: rs2063190947
seq_region_name: 17
source: dbSNP
start: 73417346
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417350
feature_type: variation
id: rs2063190964
seq_region_name: 17
source: dbSNP
start: 73417350
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417354
feature_type: variation
id: rs2063190985
seq_region_name: 17
source: dbSNP
start: 73417354
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417355
feature_type: variation
id: rs2063191008
seq_region_name: 17
source: dbSNP
start: 73417355
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417357
feature_type: variation
id: rs1053180197
seq_region_name: 17
source: dbSNP
start: 73417357
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417359
feature_type: variation
id: rs2145574677
seq_region_name: 17
source: dbSNP
start: 73417359
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417361
feature_type: variation
id: rs1159743046
seq_region_name: 17
source: dbSNP
start: 73417361
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417362
feature_type: variation
id: rs535284934
seq_region_name: 17
source: dbSNP
start: 73417362
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417363
feature_type: variation
id: rs891441841
seq_region_name: 17
source: dbSNP
start: 73417363
strand: 1
-
alleles:
- CAC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417367
feature_type: variation
id: rs1288785673
seq_region_name: 17
source: dbSNP
start: 73417365
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417367
feature_type: variation
id: rs2063191146
seq_region_name: 17
source: dbSNP
start: 73417367
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417371
feature_type: variation
id: rs2063191166
seq_region_name: 17
source: dbSNP
start: 73417371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417379
feature_type: variation
id: rs919829291
seq_region_name: 17
source: dbSNP
start: 73417379
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417383
feature_type: variation
id: rs1356232812
seq_region_name: 17
source: dbSNP
start: 73417383
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417386
feature_type: variation
id: rs573456597
seq_region_name: 17
source: dbSNP
start: 73417386
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417387
feature_type: variation
id: rs1044767517
seq_region_name: 17
source: dbSNP
start: 73417387
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417391
feature_type: variation
id: rs2063191281
seq_region_name: 17
source: dbSNP
start: 73417391
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417393
feature_type: variation
id: rs1334367575
seq_region_name: 17
source: dbSNP
start: 73417393
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417395
feature_type: variation
id: rs2063191341
seq_region_name: 17
source: dbSNP
start: 73417395
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417396
feature_type: variation
id: rs1599546442
seq_region_name: 17
source: dbSNP
start: 73417396
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417397
feature_type: variation
id: rs2063191381
seq_region_name: 17
source: dbSNP
start: 73417397
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417399
feature_type: variation
id: rs1261827081
seq_region_name: 17
source: dbSNP
start: 73417399
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417403
feature_type: variation
id: rs2063191428
seq_region_name: 17
source: dbSNP
start: 73417403
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417404
feature_type: variation
id: rs2063191452
seq_region_name: 17
source: dbSNP
start: 73417405
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417405
feature_type: variation
id: rs1043118279
seq_region_name: 17
source: dbSNP
start: 73417405
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417405
feature_type: variation
id: rs1241728310
seq_region_name: 17
source: dbSNP
start: 73417405
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417406
feature_type: variation
id: rs2063191474
seq_region_name: 17
source: dbSNP
start: 73417406
strand: 1
-
alleles:
- AAAAAAAAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417419
feature_type: variation
id: rs111684261
seq_region_name: 17
source: dbSNP
start: 73417406
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417407
feature_type: variation
id: rs2063191563
seq_region_name: 17
source: dbSNP
start: 73417407
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417412
feature_type: variation
id: rs2063191594
seq_region_name: 17
source: dbSNP
start: 73417412
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417419
feature_type: variation
id: rs1380380492
seq_region_name: 17
source: dbSNP
start: 73417419
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs1455239675
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1475565127
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417434
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063191828
seq_region_name: 17
source: dbSNP
start: 73417435
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145574890
seq_region_name: 17
source: dbSNP
start: 73417438
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063191854
seq_region_name: 17
source: dbSNP
start: 73417440
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1420372843
seq_region_name: 17
source: dbSNP
start: 73417444
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1191689315
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1011259299
seq_region_name: 17
source: dbSNP
start: 73417448
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1042958274
seq_region_name: 17
source: dbSNP
start: 73417449
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568393171
seq_region_name: 17
source: dbSNP
start: 73417449
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1262802934
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1566283
seq_region_name: 17
source: dbSNP
start: 73417454
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003334122
seq_region_name: 17
source: dbSNP
start: 73417455
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599546515
seq_region_name: 17
source: dbSNP
start: 73417457
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599546519
seq_region_name: 17
source: dbSNP
start: 73417458
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs575095790
seq_region_name: 17
source: dbSNP
start: 73417461
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746402548
seq_region_name: 17
source: dbSNP
start: 73417464
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs115782179
seq_region_name: 17
source: dbSNP
start: 73417468
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1286162142
seq_region_name: 17
source: dbSNP
start: 73417468
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs756419570
seq_region_name: 17
source: dbSNP
start: 73417470
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063192244
seq_region_name: 17
source: dbSNP
start: 73417473
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1334912187
seq_region_name: 17
source: dbSNP
start: 73417474
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs764307682
seq_region_name: 17
source: dbSNP
start: 73417475
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs969359837
seq_region_name: 17
source: dbSNP
start: 73417477
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063192366
seq_region_name: 17
source: dbSNP
start: 73417478
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs996463735
seq_region_name: 17
source: dbSNP
start: 73417483
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1486386208
seq_region_name: 17
source: dbSNP
start: 73417484
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063192446
seq_region_name: 17
source: dbSNP
start: 73417489
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417491
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417492
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1028379900
seq_region_name: 17
source: dbSNP
start: 73417494
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417495
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs953745653
seq_region_name: 17
source: dbSNP
start: 73417496
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145575049
seq_region_name: 17
source: dbSNP
start: 73417499
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063192647
seq_region_name: 17
source: dbSNP
start: 73417502
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs34147029
seq_region_name: 17
source: dbSNP
start: 73417505
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs912310824
seq_region_name: 17
source: dbSNP
start: 73417505
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs780443499
seq_region_name: 17
source: dbSNP
start: 73417509
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417514
feature_type: variation
id: rs961146321
seq_region_name: 17
source: dbSNP
start: 73417514
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1166391221
seq_region_name: 17
source: dbSNP
start: 73417515
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417517
feature_type: variation
id: rs2145575091
seq_region_name: 17
source: dbSNP
start: 73417517
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417525
feature_type: variation
id: rs1475182625
seq_region_name: 17
source: dbSNP
start: 73417525
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417530
feature_type: variation
id: rs2145575102
seq_region_name: 17
source: dbSNP
start: 73417530
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417532
feature_type: variation
id: rs2063192854
seq_region_name: 17
source: dbSNP
start: 73417532
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417535
feature_type: variation
id: rs2063192876
seq_region_name: 17
source: dbSNP
start: 73417535
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417536
feature_type: variation
id: rs2145575115
seq_region_name: 17
source: dbSNP
start: 73417536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417543
feature_type: variation
id: rs2063192896
seq_region_name: 17
source: dbSNP
start: 73417543
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417544
feature_type: variation
id: rs867323000
seq_region_name: 17
source: dbSNP
start: 73417544
strand: 1
-
alleles:
- AGGTCTAGG
- AGGTCTAGGTCTAGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417553
feature_type: variation
id: rs1195841558
seq_region_name: 17
source: dbSNP
start: 73417545
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417546
feature_type: variation
id: rs1599546616
seq_region_name: 17
source: dbSNP
start: 73417546
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417548
feature_type: variation
id: rs1599546620
seq_region_name: 17
source: dbSNP
start: 73417548
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417549
feature_type: variation
id: rs1431789163
seq_region_name: 17
source: dbSNP
start: 73417549
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417552
feature_type: variation
id: rs1252995794
seq_region_name: 17
source: dbSNP
start: 73417552
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417554
feature_type: variation
id: rs2063193081
seq_region_name: 17
source: dbSNP
start: 73417554
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417555
feature_type: variation
id: rs1214788940
seq_region_name: 17
source: dbSNP
start: 73417555
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417558
feature_type: variation
id: rs954946883
seq_region_name: 17
source: dbSNP
start: 73417558
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417561
feature_type: variation
id: rs1274453429
seq_region_name: 17
source: dbSNP
start: 73417561
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417564
feature_type: variation
id: rs1410694932
seq_region_name: 17
source: dbSNP
start: 73417564
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417571
feature_type: variation
id: rs1193748316
seq_region_name: 17
source: dbSNP
start: 73417571
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417574
feature_type: variation
id: rs749653907
seq_region_name: 17
source: dbSNP
start: 73417574
strand: 1
-
alleles:
- TTT
- TTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417577
feature_type: variation
id: rs2063193257
seq_region_name: 17
source: dbSNP
start: 73417575
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417576
feature_type: variation
id: rs2063193284
seq_region_name: 17
source: dbSNP
start: 73417576
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417585
feature_type: variation
id: rs1014981371
seq_region_name: 17
source: dbSNP
start: 73417585
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417588
feature_type: variation
id: rs1158605679
seq_region_name: 17
source: dbSNP
start: 73417588
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417589
feature_type: variation
id: rs931193726
seq_region_name: 17
source: dbSNP
start: 73417589
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417590
feature_type: variation
id: rs1302597669
seq_region_name: 17
source: dbSNP
start: 73417590
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417593
feature_type: variation
id: rs1441482823
seq_region_name: 17
source: dbSNP
start: 73417593
strand: 1
-
alleles:
- AACCA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417599
feature_type: variation
id: rs1044325177
seq_region_name: 17
source: dbSNP
start: 73417595
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417598
feature_type: variation
id: rs768918527
seq_region_name: 17
source: dbSNP
start: 73417598
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417603
feature_type: variation
id: rs2063193503
seq_region_name: 17
source: dbSNP
start: 73417600
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417603
feature_type: variation
id: rs183091722
seq_region_name: 17
source: dbSNP
start: 73417603
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417609
feature_type: variation
id: rs2063193557
seq_region_name: 17
source: dbSNP
start: 73417609
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417610
feature_type: variation
id: rs973385509
seq_region_name: 17
source: dbSNP
start: 73417610
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417612
feature_type: variation
id: rs938691986
seq_region_name: 17
source: dbSNP
start: 73417612
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417616
feature_type: variation
id: rs1663682184
seq_region_name: 17
source: dbSNP
start: 73417616
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417621
feature_type: variation
id: rs2063193621
seq_region_name: 17
source: dbSNP
start: 73417621
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417623
feature_type: variation
id: rs2063193644
seq_region_name: 17
source: dbSNP
start: 73417623
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417624
feature_type: variation
id: rs2063193668
seq_region_name: 17
source: dbSNP
start: 73417624
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417625
feature_type: variation
id: rs563756578
seq_region_name: 17
source: dbSNP
start: 73417625
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73417801
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73417808
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73417809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73417811
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73417815
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73417816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73417820
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1230786944
seq_region_name: 17
source: dbSNP
start: 73417821
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063195362
seq_region_name: 17
source: dbSNP
start: 73417826
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1406505378
seq_region_name: 17
source: dbSNP
start: 73417829
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417832
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id: rs2063195390
seq_region_name: 17
source: dbSNP
start: 73417832
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063195411
seq_region_name: 17
source: dbSNP
start: 73417834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417836
feature_type: variation
id: rs994795843
seq_region_name: 17
source: dbSNP
start: 73417836
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417840
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73417847
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1232901759
seq_region_name: 17
source: dbSNP
start: 73417848
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417853
feature_type: variation
id: rs1023619559
seq_region_name: 17
source: dbSNP
start: 73417853
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417855
feature_type: variation
id: rs2063195537
seq_region_name: 17
source: dbSNP
start: 73417855
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417856
feature_type: variation
id: rs2063195563
seq_region_name: 17
source: dbSNP
start: 73417856
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417857
feature_type: variation
id: rs2063195596
seq_region_name: 17
source: dbSNP
start: 73417857
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417860
feature_type: variation
id: rs2063195618
seq_region_name: 17
source: dbSNP
start: 73417860
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417864
feature_type: variation
id: rs542479277
seq_region_name: 17
source: dbSNP
start: 73417864
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417865
feature_type: variation
id: rs1029249695
seq_region_name: 17
source: dbSNP
start: 73417865
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417866
feature_type: variation
id: rs2145575683
seq_region_name: 17
source: dbSNP
start: 73417866
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417870
feature_type: variation
id: rs1256335279
seq_region_name: 17
source: dbSNP
start: 73417870
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417873
feature_type: variation
id: rs1211403278
seq_region_name: 17
source: dbSNP
start: 73417873
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417875
feature_type: variation
id: rs890742860
seq_region_name: 17
source: dbSNP
start: 73417875
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417885
feature_type: variation
id: rs982362673
seq_region_name: 17
source: dbSNP
start: 73417885
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417886
feature_type: variation
id: rs138517451
seq_region_name: 17
source: dbSNP
start: 73417886
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417888
feature_type: variation
id: rs1351525155
seq_region_name: 17
source: dbSNP
start: 73417888
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417896
feature_type: variation
id: rs1281316141
seq_region_name: 17
source: dbSNP
start: 73417896
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417905
feature_type: variation
id: rs2063195893
seq_region_name: 17
source: dbSNP
start: 73417905
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417907
feature_type: variation
id: rs1276574318
seq_region_name: 17
source: dbSNP
start: 73417907
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417907
feature_type: variation
id: rs2145575721
seq_region_name: 17
source: dbSNP
start: 73417907
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417908
feature_type: variation
id: rs2063195950
seq_region_name: 17
source: dbSNP
start: 73417908
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417909
feature_type: variation
id: rs1412979868
seq_region_name: 17
source: dbSNP
start: 73417909
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417913
feature_type: variation
id: rs1818532763
seq_region_name: 17
source: dbSNP
start: 73417913
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417914
feature_type: variation
id: rs1355118194
seq_region_name: 17
source: dbSNP
start: 73417914
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417915
feature_type: variation
id: rs2063196011
seq_region_name: 17
source: dbSNP
start: 73417915
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417928
feature_type: variation
id: rs1799557848
seq_region_name: 17
source: dbSNP
start: 73417928
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417930
feature_type: variation
id: rs2063196036
seq_region_name: 17
source: dbSNP
start: 73417929
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417930
feature_type: variation
id: rs2063196058
seq_region_name: 17
source: dbSNP
start: 73417930
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417937
feature_type: variation
id: rs552668423
seq_region_name: 17
source: dbSNP
start: 73417937
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417941
feature_type: variation
id: rs60476533
seq_region_name: 17
source: dbSNP
start: 73417941
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417947
feature_type: variation
id: rs1313702309
seq_region_name: 17
source: dbSNP
start: 73417947
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417952
feature_type: variation
id: rs2063196184
seq_region_name: 17
source: dbSNP
start: 73417952
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417953
feature_type: variation
id: rs1019262310
seq_region_name: 17
source: dbSNP
start: 73417953
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417954
feature_type: variation
id: rs1035694217
seq_region_name: 17
source: dbSNP
start: 73417954
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417955
feature_type: variation
id: rs1318266664
seq_region_name: 17
source: dbSNP
start: 73417955
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417956
feature_type: variation
id: rs2063196278
seq_region_name: 17
source: dbSNP
start: 73417956
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417959
feature_type: variation
id: rs1599546911
seq_region_name: 17
source: dbSNP
start: 73417959
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417963
feature_type: variation
id: rs2063196327
seq_region_name: 17
source: dbSNP
start: 73417963
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417968
feature_type: variation
id: rs2063196355
seq_region_name: 17
source: dbSNP
start: 73417968
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417974
feature_type: variation
id: rs2063196380
seq_region_name: 17
source: dbSNP
start: 73417974
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417975
feature_type: variation
id: rs2063196416
seq_region_name: 17
source: dbSNP
start: 73417975
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417976
feature_type: variation
id: rs961087712
seq_region_name: 17
source: dbSNP
start: 73417976
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417980
feature_type: variation
id: rs2063196463
seq_region_name: 17
source: dbSNP
start: 73417980
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417981
feature_type: variation
id: rs956858875
seq_region_name: 17
source: dbSNP
start: 73417981
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417983
feature_type: variation
id: rs988309039
seq_region_name: 17
source: dbSNP
start: 73417983
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417986
feature_type: variation
id: rs1160803460
seq_region_name: 17
source: dbSNP
start: 73417986
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417988
feature_type: variation
id: rs1473929858
seq_region_name: 17
source: dbSNP
start: 73417988
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417997
feature_type: variation
id: rs1027200094
seq_region_name: 17
source: dbSNP
start: 73417997
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73417999
feature_type: variation
id: rs113276093
seq_region_name: 17
source: dbSNP
start: 73417999
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418003
feature_type: variation
id: rs2063196640
seq_region_name: 17
source: dbSNP
start: 73418003
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418006
feature_type: variation
id: rs2145575889
seq_region_name: 17
source: dbSNP
start: 73418006
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418008
feature_type: variation
id: rs1404127695
seq_region_name: 17
source: dbSNP
start: 73418008
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418009
feature_type: variation
id: rs1415120051
seq_region_name: 17
source: dbSNP
start: 73418009
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418010
feature_type: variation
id: rs1312251636
seq_region_name: 17
source: dbSNP
start: 73418010
strand: 1
-
alleles:
- "-"
- GTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418010
feature_type: variation
id: rs775751694
seq_region_name: 17
source: dbSNP
start: 73418011
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418011
feature_type: variation
id: rs1393023171
seq_region_name: 17
source: dbSNP
start: 73418011
strand: 1
-
alleles:
- T
- TGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418011
feature_type: variation
id: rs1555765778
seq_region_name: 17
source: dbSNP
start: 73418011
strand: 1
-
alleles:
- TT
- TTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418012
feature_type: variation
id: rs2063196808
seq_region_name: 17
source: dbSNP
start: 73418011
strand: 1
-
alleles:
- TTT
- TTTGTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418013
feature_type: variation
id: rs1555765779
seq_region_name: 17
source: dbSNP
start: 73418011
strand: 1
-
alleles:
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418028
feature_type: variation
id: rs397689294
seq_region_name: 17
source: dbSNP
start: 73418011
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418011
feature_type: variation
id: rs10653153
seq_region_name: 17
source: dbSNP
start: 73418012
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418012
feature_type: variation
id: rs1425146747
seq_region_name: 17
source: dbSNP
start: 73418012
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418014
feature_type: variation
id: rs2145576007
seq_region_name: 17
source: dbSNP
start: 73418012
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418013
feature_type: variation
id: rs1172296057
seq_region_name: 17
source: dbSNP
start: 73418013
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418016
feature_type: variation
id: rs1416909748
seq_region_name: 17
source: dbSNP
start: 73418014
strand: 1
-
alleles:
- TTTT
- TTTTCTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418018
feature_type: variation
id: rs2063197423
seq_region_name: 17
source: dbSNP
start: 73418015
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418016
feature_type: variation
id: rs2063197447
seq_region_name: 17
source: dbSNP
start: 73418016
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418018
feature_type: variation
id: rs2063197462
seq_region_name: 17
source: dbSNP
start: 73418016
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418017
feature_type: variation
id: rs947155781
seq_region_name: 17
source: dbSNP
start: 73418017
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418017
feature_type: variation
id: rs2063197507
seq_region_name: 17
source: dbSNP
start: 73418018
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418018
feature_type: variation
id: rs2145576049
seq_region_name: 17
source: dbSNP
start: 73418018
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418020
feature_type: variation
id: rs1185766994
seq_region_name: 17
source: dbSNP
start: 73418018
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418019
feature_type: variation
id: rs2145576062
seq_region_name: 17
source: dbSNP
start: 73418019
strand: 1
-
alleles:
- TTTT
- TTTTGTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418022
feature_type: variation
id: rs1401644570
seq_region_name: 17
source: dbSNP
start: 73418019
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418019
feature_type: variation
id: rs1410570798
seq_region_name: 17
source: dbSNP
start: 73418020
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418020
feature_type: variation
id: rs1211672979
seq_region_name: 17
source: dbSNP
start: 73418020
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418020
feature_type: variation
id: rs2063197754
seq_region_name: 17
source: dbSNP
start: 73418020
strand: 1
-
alleles:
- TT
- TTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418021
feature_type: variation
id: rs2063197786
seq_region_name: 17
source: dbSNP
start: 73418020
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418022
feature_type: variation
id: rs1555765782
seq_region_name: 17
source: dbSNP
start: 73418020
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418020
feature_type: variation
id: rs1555765784
seq_region_name: 17
source: dbSNP
start: 73418021
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418021
feature_type: variation
id: rs978412936
seq_region_name: 17
source: dbSNP
start: 73418021
strand: 1
-
alleles:
- TT
- TTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418022
feature_type: variation
id: rs1568393515
seq_region_name: 17
source: dbSNP
start: 73418021
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418023
feature_type: variation
id: rs1468105694
seq_region_name: 17
source: dbSNP
start: 73418021
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418021
feature_type: variation
id: rs938607924
seq_region_name: 17
source: dbSNP
start: 73418022
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418024
feature_type: variation
id: rs1568393524
seq_region_name: 17
source: dbSNP
start: 73418022
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418023
feature_type: variation
id: rs921642389
seq_region_name: 17
source: dbSNP
start: 73418023
strand: 1
-
alleles:
- TT
- TTGTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418024
feature_type: variation
id: rs992810930
seq_region_name: 17
source: dbSNP
start: 73418023
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418025
feature_type: variation
id: rs1555765787
seq_region_name: 17
source: dbSNP
start: 73418023
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418024
feature_type: variation
id: rs76689547
seq_region_name: 17
source: dbSNP
start: 73418024
strand: 1
-
alleles:
- TTT
- TTTCTTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418026
feature_type: variation
id: rs1243108828
seq_region_name: 17
source: dbSNP
start: 73418024
strand: 1
-
alleles:
- TTTT
- TTTTGTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418027
feature_type: variation
id: rs2063198102
seq_region_name: 17
source: dbSNP
start: 73418024
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418024
feature_type: variation
id: rs201160362
seq_region_name: 17
source: dbSNP
start: 73418025
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418025
feature_type: variation
id: rs534687006
seq_region_name: 17
source: dbSNP
start: 73418025
strand: 1
-
alleles:
- T
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418025
feature_type: variation
id: rs2063198170
seq_region_name: 17
source: dbSNP
start: 73418025
strand: 1
-
alleles:
- TTT
- TTTGTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418027
feature_type: variation
id: rs1555765790
seq_region_name: 17
source: dbSNP
start: 73418025
strand: 1
-
alleles:
- "-"
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418025
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418030
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1270626538
seq_region_name: 17
source: dbSNP
start: 73418034
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1297797096
seq_region_name: 17
source: dbSNP
start: 73418035
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1480446374
seq_region_name: 17
source: dbSNP
start: 73418035
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063198632
seq_region_name: 17
source: dbSNP
start: 73418035
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418037
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599547124
seq_region_name: 17
source: dbSNP
start: 73418037
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1422956976
seq_region_name: 17
source: dbSNP
start: 73418038
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063198718
seq_region_name: 17
source: dbSNP
start: 73418039
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1391728218
seq_region_name: 17
source: dbSNP
start: 73418041
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1372904391
seq_region_name: 17
source: dbSNP
start: 73418044
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs940497251
seq_region_name: 17
source: dbSNP
start: 73418046
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1036193127
seq_region_name: 17
source: dbSNP
start: 73418047
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418050
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1339531667
seq_region_name: 17
source: dbSNP
start: 73418051
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1196980735
seq_region_name: 17
source: dbSNP
start: 73418052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs994904656
seq_region_name: 17
source: dbSNP
start: 73418055
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063198958
seq_region_name: 17
source: dbSNP
start: 73418059
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1023693279
seq_region_name: 17
source: dbSNP
start: 73418061
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs890701179
seq_region_name: 17
source: dbSNP
start: 73418065
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063199022
seq_region_name: 17
source: dbSNP
start: 73418067
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1234074531
seq_region_name: 17
source: dbSNP
start: 73418068
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs905163307
seq_region_name: 17
source: dbSNP
start: 73418070
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1436797362
seq_region_name: 17
source: dbSNP
start: 73418071
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003959038
seq_region_name: 17
source: dbSNP
start: 73418077
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145576350
seq_region_name: 17
source: dbSNP
start: 73418082
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063199169
seq_region_name: 17
source: dbSNP
start: 73418084
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599547188
seq_region_name: 17
source: dbSNP
start: 73418088
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063199209
seq_region_name: 17
source: dbSNP
start: 73418089
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1035237082
seq_region_name: 17
source: dbSNP
start: 73418090
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418092
feature_type: variation
id: rs1370458776
seq_region_name: 17
source: dbSNP
start: 73418092
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418093
feature_type: variation
id: rs2063199288
seq_region_name: 17
source: dbSNP
start: 73418093
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418098
feature_type: variation
id: rs1297268171
seq_region_name: 17
source: dbSNP
start: 73418098
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418100
feature_type: variation
id: rs1193872661
seq_region_name: 17
source: dbSNP
start: 73418100
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418103
feature_type: variation
id: rs1372216306
seq_region_name: 17
source: dbSNP
start: 73418103
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418104
feature_type: variation
id: rs1805517717
seq_region_name: 17
source: dbSNP
start: 73418104
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418108
feature_type: variation
id: rs2063199362
seq_region_name: 17
source: dbSNP
start: 73418108
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418113
feature_type: variation
id: rs2063199387
seq_region_name: 17
source: dbSNP
start: 73418113
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418119
feature_type: variation
id: rs957215123
seq_region_name: 17
source: dbSNP
start: 73418119
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418122
feature_type: variation
id: rs143427962
seq_region_name: 17
source: dbSNP
start: 73418122
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418124
feature_type: variation
id: rs2063199459
seq_region_name: 17
source: dbSNP
start: 73418124
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418127
feature_type: variation
id: rs2063199484
seq_region_name: 17
source: dbSNP
start: 73418127
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418128
feature_type: variation
id: rs1433847996
seq_region_name: 17
source: dbSNP
start: 73418128
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418130
feature_type: variation
id: rs2063199535
seq_region_name: 17
source: dbSNP
start: 73418130
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418138
feature_type: variation
id: rs1395684891
seq_region_name: 17
source: dbSNP
start: 73418138
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418140
feature_type: variation
id: rs1178056382
seq_region_name: 17
source: dbSNP
start: 73418140
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418141
feature_type: variation
id: rs2063199622
seq_region_name: 17
source: dbSNP
start: 73418141
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418142
feature_type: variation
id: rs1417415593
seq_region_name: 17
source: dbSNP
start: 73418142
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418143
feature_type: variation
id: rs1019210310
seq_region_name: 17
source: dbSNP
start: 73418143
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418144
feature_type: variation
id: rs2063199698
seq_region_name: 17
source: dbSNP
start: 73418144
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418148
feature_type: variation
id: rs1022501804
seq_region_name: 17
source: dbSNP
start: 73418148
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418149
feature_type: variation
id: rs762186691
seq_region_name: 17
source: dbSNP
start: 73418149
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418151
feature_type: variation
id: rs1192349152
seq_region_name: 17
source: dbSNP
start: 73418151
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418152
feature_type: variation
id: rs968439406
seq_region_name: 17
source: dbSNP
start: 73418152
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418153
feature_type: variation
id: rs2063199851
seq_region_name: 17
source: dbSNP
start: 73418153
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418166
feature_type: variation
id: rs2063199883
seq_region_name: 17
source: dbSNP
start: 73418166
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418170
feature_type: variation
id: rs2145576536
seq_region_name: 17
source: dbSNP
start: 73418170
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418171
feature_type: variation
id: rs2145576544
seq_region_name: 17
source: dbSNP
start: 73418171
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418172
feature_type: variation
id: rs1377518075
seq_region_name: 17
source: dbSNP
start: 73418172
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418173
feature_type: variation
id: rs1210690594
seq_region_name: 17
source: dbSNP
start: 73418173
strand: 1
-
alleles:
- ATTTTTGTATTTTT
- ATTTTT
- ATTTTTGTATTTTTGTATTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418187
feature_type: variation
id: rs760815426
seq_region_name: 17
source: dbSNP
start: 73418174
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418177
feature_type: variation
id: rs1258293096
seq_region_name: 17
source: dbSNP
start: 73418177
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418178
feature_type: variation
id: rs2063200000
seq_region_name: 17
source: dbSNP
start: 73418178
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418190
feature_type: variation
id: rs1237448118
seq_region_name: 17
source: dbSNP
start: 73418190
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418192
feature_type: variation
id: rs2063200047
seq_region_name: 17
source: dbSNP
start: 73418192
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418196
feature_type: variation
id: rs2145576598
seq_region_name: 17
source: dbSNP
start: 73418196
strand: 1
-
alleles:
- GGGGTTTCACCA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418208
feature_type: variation
id: rs2063200070
seq_region_name: 17
source: dbSNP
start: 73418197
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418199
feature_type: variation
id: rs978486646
seq_region_name: 17
source: dbSNP
start: 73418199
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418203
feature_type: variation
id: rs1169669218
seq_region_name: 17
source: dbSNP
start: 73418203
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418208
feature_type: variation
id: rs1228446178
seq_region_name: 17
source: dbSNP
start: 73418208
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418210
feature_type: variation
id: rs2063200158
seq_region_name: 17
source: dbSNP
start: 73418210
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418212
feature_type: variation
id: rs568252814
seq_region_name: 17
source: dbSNP
start: 73418212
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418215
feature_type: variation
id: rs2063200203
seq_region_name: 17
source: dbSNP
start: 73418215
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418216
feature_type: variation
id: rs993836817
seq_region_name: 17
source: dbSNP
start: 73418216
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418231
feature_type: variation
id: rs2063200254
seq_region_name: 17
source: dbSNP
start: 73418231
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418236
feature_type: variation
id: rs1809072522
seq_region_name: 17
source: dbSNP
start: 73418236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418238
feature_type: variation
id: rs2063200274
seq_region_name: 17
source: dbSNP
start: 73418238
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73418320
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73418323
strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73418330
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73418342
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73418352
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73418356
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418357
strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73418374
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73418379
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73418383
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73418388
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418391
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418401
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73418403
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418424
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418425
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418426
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418431
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418433
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1370390741
seq_region_name: 17
source: dbSNP
start: 73418434
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063201715
seq_region_name: 17
source: dbSNP
start: 73418446
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1191555436
seq_region_name: 17
source: dbSNP
start: 73418450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs762718621
seq_region_name: 17
source: dbSNP
start: 73418452
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418455
feature_type: variation
id: rs1212161579
seq_region_name: 17
source: dbSNP
start: 73418455
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs563102492
seq_region_name: 17
source: dbSNP
start: 73418456
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73418457
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418458
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003542328
seq_region_name: 17
source: dbSNP
start: 73418463
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73418464
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418465
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418467
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418471
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs944925695
seq_region_name: 17
source: dbSNP
start: 73418472
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418489
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063202049
seq_region_name: 17
source: dbSNP
start: 73418490
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1266831554
seq_region_name: 17
source: dbSNP
start: 73418492
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418499
feature_type: variation
id: rs1225054945
seq_region_name: 17
source: dbSNP
start: 73418499
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418508
feature_type: variation
id: rs140292151
seq_region_name: 17
source: dbSNP
start: 73418508
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418513
feature_type: variation
id: rs1599547481
seq_region_name: 17
source: dbSNP
start: 73418513
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418517
feature_type: variation
id: rs187750033
seq_region_name: 17
source: dbSNP
start: 73418517
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418519
feature_type: variation
id: rs1437132897
seq_region_name: 17
source: dbSNP
start: 73418519
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418525
feature_type: variation
id: rs2063202204
seq_region_name: 17
source: dbSNP
start: 73418525
strand: 1
-
alleles:
- TGTGTACATG
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418536
feature_type: variation
id: rs1368914718
seq_region_name: 17
source: dbSNP
start: 73418527
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418533
feature_type: variation
id: rs754586324
seq_region_name: 17
source: dbSNP
start: 73418533
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418538
feature_type: variation
id: rs1325357806
seq_region_name: 17
source: dbSNP
start: 73418538
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418539
feature_type: variation
id: rs2063202286
seq_region_name: 17
source: dbSNP
start: 73418539
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418546
feature_type: variation
id: rs1406008705
seq_region_name: 17
source: dbSNP
start: 73418546
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73418799
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73418806
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418808
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418810
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418812
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73418813
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418814
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418815
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145577553
seq_region_name: 17
source: dbSNP
start: 73418822
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063204073
seq_region_name: 17
source: dbSNP
start: 73418824
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73418827
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418827
strand: 1
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alleles:
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- A
assembly_name: GRCh38
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strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73418899
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73418901
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73418913
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418915
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063204790
seq_region_name: 17
source: dbSNP
start: 73418917
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063204847
seq_region_name: 17
source: dbSNP
start: 73418919
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418926
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73418927
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418935
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73418939
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418940
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs866274159
seq_region_name: 17
source: dbSNP
start: 73418941
strand: 1
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alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73418947
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418950
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1314111350
seq_region_name: 17
source: dbSNP
start: 73418954
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1009586458
seq_region_name: 17
source: dbSNP
start: 73418956
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418957
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418958
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73418969
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73418970
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1043969669
seq_region_name: 17
source: dbSNP
start: 73418971
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418977
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418979
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73418988
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs895607161
seq_region_name: 17
source: dbSNP
start: 73418992
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs6501633
seq_region_name: 17
source: dbSNP
start: 73418993
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs79687016
seq_region_name: 17
source: dbSNP
start: 73418996
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs779157394
seq_region_name: 17
source: dbSNP
start: 73419000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063205463
seq_region_name: 17
source: dbSNP
start: 73419002
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419005
feature_type: variation
id: rs2063205488
seq_region_name: 17
source: dbSNP
start: 73419005
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063205509
seq_region_name: 17
source: dbSNP
start: 73419006
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599547864
seq_region_name: 17
source: dbSNP
start: 73419014
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063205546
seq_region_name: 17
source: dbSNP
start: 73419018
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419020
feature_type: variation
id: rs8072292
seq_region_name: 17
source: dbSNP
start: 73419020
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419024
feature_type: variation
id: rs1436426626
seq_region_name: 17
source: dbSNP
start: 73419024
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419029
feature_type: variation
id: rs2063205673
seq_region_name: 17
source: dbSNP
start: 73419025
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419026
feature_type: variation
id: rs2063205702
seq_region_name: 17
source: dbSNP
start: 73419026
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419036
feature_type: variation
id: rs1568394017
seq_region_name: 17
source: dbSNP
start: 73419036
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419037
feature_type: variation
id: rs1367925928
seq_region_name: 17
source: dbSNP
start: 73419037
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419038
feature_type: variation
id: rs1032978788
seq_region_name: 17
source: dbSNP
start: 73419038
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419042
feature_type: variation
id: rs1599547884
seq_region_name: 17
source: dbSNP
start: 73419042
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419043
feature_type: variation
id: rs2063205847
seq_region_name: 17
source: dbSNP
start: 73419043
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419047
feature_type: variation
id: rs2063205866
seq_region_name: 17
source: dbSNP
start: 73419047
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419051
feature_type: variation
id: rs953505815
seq_region_name: 17
source: dbSNP
start: 73419051
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419057
feature_type: variation
id: rs2063205897
seq_region_name: 17
source: dbSNP
start: 73419057
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419059
feature_type: variation
id: rs2145577984
seq_region_name: 17
source: dbSNP
start: 73419059
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419062
feature_type: variation
id: rs149281848
seq_region_name: 17
source: dbSNP
start: 73419062
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419063
feature_type: variation
id: rs911966296
seq_region_name: 17
source: dbSNP
start: 73419063
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419066
feature_type: variation
id: rs1406934910
seq_region_name: 17
source: dbSNP
start: 73419066
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419069
feature_type: variation
id: rs557878459
seq_region_name: 17
source: dbSNP
start: 73419069
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419073
feature_type: variation
id: rs2063206036
seq_region_name: 17
source: dbSNP
start: 73419073
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419075
feature_type: variation
id: rs2063206061
seq_region_name: 17
source: dbSNP
start: 73419075
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419084
feature_type: variation
id: rs2063206092
seq_region_name: 17
source: dbSNP
start: 73419084
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419085
feature_type: variation
id: rs2063206105
seq_region_name: 17
source: dbSNP
start: 73419085
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419086
feature_type: variation
id: rs2063206131
seq_region_name: 17
source: dbSNP
start: 73419086
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419097
feature_type: variation
id: rs1167926327
seq_region_name: 17
source: dbSNP
start: 73419097
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419099
feature_type: variation
id: rs2063206176
seq_region_name: 17
source: dbSNP
start: 73419099
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419103
feature_type: variation
id: rs566454161
seq_region_name: 17
source: dbSNP
start: 73419103
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419104
feature_type: variation
id: rs2063206226
seq_region_name: 17
source: dbSNP
start: 73419104
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419105
feature_type: variation
id: rs376374660
seq_region_name: 17
source: dbSNP
start: 73419105
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419106
feature_type: variation
id: rs8071352
seq_region_name: 17
source: dbSNP
start: 73419106
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419110
feature_type: variation
id: rs555092431
seq_region_name: 17
source: dbSNP
start: 73419110
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419116
feature_type: variation
id: rs1251460042
seq_region_name: 17
source: dbSNP
start: 73419112
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419114
feature_type: variation
id: rs2063206388
seq_region_name: 17
source: dbSNP
start: 73419114
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419115
feature_type: variation
id: rs1247575053
seq_region_name: 17
source: dbSNP
start: 73419115
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419120
feature_type: variation
id: rs1568394046
seq_region_name: 17
source: dbSNP
start: 73419120
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419125
feature_type: variation
id: rs768826989
seq_region_name: 17
source: dbSNP
start: 73419125
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419126
feature_type: variation
id: rs1256428061
seq_region_name: 17
source: dbSNP
start: 73419126
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419128
feature_type: variation
id: rs781606393
seq_region_name: 17
source: dbSNP
start: 73419128
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419130
feature_type: variation
id: rs1274415469
seq_region_name: 17
source: dbSNP
start: 73419130
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419135
feature_type: variation
id: rs536909782
seq_region_name: 17
source: dbSNP
start: 73419135
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419137
feature_type: variation
id: rs1599547952
seq_region_name: 17
source: dbSNP
start: 73419137
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419138
feature_type: variation
id: rs1185575103
seq_region_name: 17
source: dbSNP
start: 73419138
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419139
feature_type: variation
id: rs770391874
seq_region_name: 17
source: dbSNP
start: 73419139
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419140
feature_type: variation
id: rs369463368
seq_region_name: 17
source: dbSNP
start: 73419140
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419142
feature_type: variation
id: rs372996990
seq_region_name: 17
source: dbSNP
start: 73419142
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419143
feature_type: variation
id: rs1373374420
seq_region_name: 17
source: dbSNP
start: 73419143
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419144
feature_type: variation
id: rs2063206707
seq_region_name: 17
source: dbSNP
start: 73419144
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419145
feature_type: variation
id: rs2063206733
seq_region_name: 17
source: dbSNP
start: 73419145
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419147
feature_type: variation
id: rs770407721
seq_region_name: 17
source: dbSNP
start: 73419147
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419150
feature_type: variation
id: rs1463352631
seq_region_name: 17
source: dbSNP
start: 73419147
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419148
feature_type: variation
id: rs777972340
seq_region_name: 17
source: dbSNP
start: 73419148
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419149
feature_type: variation
id: rs1470038277
seq_region_name: 17
source: dbSNP
start: 73419149
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419152
feature_type: variation
id: rs2063206869
seq_region_name: 17
source: dbSNP
start: 73419152
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419154
feature_type: variation
id: rs1293801941
seq_region_name: 17
source: dbSNP
start: 73419152
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419153
feature_type: variation
id: rs1438128401
seq_region_name: 17
source: dbSNP
start: 73419153
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419154
feature_type: variation
id: rs1352360553
seq_region_name: 17
source: dbSNP
start: 73419154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73419159
feature_type: variation
id: rs1338110123
seq_region_name: 17
source: dbSNP
start: 73419159
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73419162
feature_type: variation
id: rs1307203960
seq_region_name: 17
source: dbSNP
start: 73419162
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73419163
feature_type: variation
id: rs1380027969
seq_region_name: 17
source: dbSNP
start: 73419163
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73419168
feature_type: variation
id: rs374370689
seq_region_name: 17
source: dbSNP
start: 73419168
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419169
feature_type: variation
id: rs1312656494
seq_region_name: 17
source: dbSNP
start: 73419169
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419171
feature_type: variation
id: rs376999956
seq_region_name: 17
source: dbSNP
start: 73419171
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419172
feature_type: variation
id: rs767128211
seq_region_name: 17
source: dbSNP
start: 73419172
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419173
feature_type: variation
id: rs775237906
seq_region_name: 17
source: dbSNP
start: 73419173
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419174
feature_type: variation
id: rs1317500337
seq_region_name: 17
source: dbSNP
start: 73419174
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419177
feature_type: variation
id: rs1599548023
seq_region_name: 17
source: dbSNP
start: 73419177
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419178
feature_type: variation
id: rs760424979
seq_region_name: 17
source: dbSNP
start: 73419178
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419180
feature_type: variation
id: rs2063207250
seq_region_name: 17
source: dbSNP
start: 73419180
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419185
feature_type: variation
id: rs930882595
seq_region_name: 17
source: dbSNP
start: 73419185
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419190
feature_type: variation
id: rs1425926572
seq_region_name: 17
source: dbSNP
start: 73419190
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419193
feature_type: variation
id: rs763895602
seq_region_name: 17
source: dbSNP
start: 73419193
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419195
feature_type: variation
id: rs1482324154
seq_region_name: 17
source: dbSNP
start: 73419195
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73419197
feature_type: variation
id: rs2063207409
seq_region_name: 17
source: dbSNP
start: 73419197
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419201
feature_type: variation
id: rs1599548048
seq_region_name: 17
source: dbSNP
start: 73419201
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419202
feature_type: variation
id: rs1199758118
seq_region_name: 17
source: dbSNP
start: 73419202
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419204
feature_type: variation
id: rs753714823
seq_region_name: 17
source: dbSNP
start: 73419204
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419207
feature_type: variation
id: rs757187447
seq_region_name: 17
source: dbSNP
start: 73419207
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419209
feature_type: variation
id: rs766473739
seq_region_name: 17
source: dbSNP
start: 73419209
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419211
feature_type: variation
id: rs2063207567
seq_region_name: 17
source: dbSNP
start: 73419211
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419213
feature_type: variation
id: rs751647060
seq_region_name: 17
source: dbSNP
start: 73419213
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73419214
feature_type: variation
id: rs370273790
seq_region_name: 17
source: dbSNP
start: 73419214
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419215
feature_type: variation
id: rs755205056
seq_region_name: 17
source: dbSNP
start: 73419215
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419217
feature_type: variation
id: rs2063207689
seq_region_name: 17
source: dbSNP
start: 73419217
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73419218
feature_type: variation
id: rs781308580
seq_region_name: 17
source: dbSNP
start: 73419218
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419230
feature_type: variation
id: rs1251284813
seq_region_name: 17
source: dbSNP
start: 73419230
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419231
feature_type: variation
id: rs867396426
seq_region_name: 17
source: dbSNP
start: 73419231
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419237
feature_type: variation
id: rs748410857
seq_region_name: 17
source: dbSNP
start: 73419237
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419239
feature_type: variation
id: rs756491454
seq_region_name: 17
source: dbSNP
start: 73419239
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419240
feature_type: variation
id: rs201725612
seq_region_name: 17
source: dbSNP
start: 73419240
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419241
feature_type: variation
id: rs749808824
seq_region_name: 17
source: dbSNP
start: 73419241
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419245
feature_type: variation
id: rs771402658
seq_region_name: 17
source: dbSNP
start: 73419245
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419247
feature_type: variation
id: rs773893762
seq_region_name: 17
source: dbSNP
start: 73419247
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73419248
feature_type: variation
id: rs376485292
seq_region_name: 17
source: dbSNP
start: 73419248
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73419251
feature_type: variation
id: rs112936861
seq_region_name: 17
source: dbSNP
start: 73419251
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419252
feature_type: variation
id: rs201245646
seq_region_name: 17
source: dbSNP
start: 73419252
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419255
feature_type: variation
id: rs895556157
seq_region_name: 17
source: dbSNP
start: 73419255
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419256
feature_type: variation
id: rs760330544
seq_region_name: 17
source: dbSNP
start: 73419256
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73419257
feature_type: variation
id: rs370423133
seq_region_name: 17
source: dbSNP
start: 73419257
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419258
feature_type: variation
id: rs570731428
seq_region_name: 17
source: dbSNP
start: 73419258
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419260
feature_type: variation
id: rs2063208151
seq_region_name: 17
source: dbSNP
start: 73419260
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419261
feature_type: variation
id: rs1262122124
seq_region_name: 17
source: dbSNP
start: 73419261
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419263
feature_type: variation
id: rs761795011
seq_region_name: 17
source: dbSNP
start: 73419263
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419264
feature_type: variation
id: rs144488293
seq_region_name: 17
source: dbSNP
start: 73419264
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419267
feature_type: variation
id: rs1422664592
seq_region_name: 17
source: dbSNP
start: 73419267
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419268
feature_type: variation
id: rs751627771
seq_region_name: 17
source: dbSNP
start: 73419268
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419273
feature_type: variation
id: rs754972679
seq_region_name: 17
source: dbSNP
start: 73419273
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419274
feature_type: variation
id: rs1365097475
seq_region_name: 17
source: dbSNP
start: 73419274
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419275
feature_type: variation
id: rs767649005
seq_region_name: 17
source: dbSNP
start: 73419275
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419276
feature_type: variation
id: rs1296900683
seq_region_name: 17
source: dbSNP
start: 73419276
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419277
feature_type: variation
id: rs2145578668
seq_region_name: 17
source: dbSNP
start: 73419277
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419278
feature_type: variation
id: rs1360233241
seq_region_name: 17
source: dbSNP
start: 73419278
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419279
feature_type: variation
id: rs371984433
seq_region_name: 17
source: dbSNP
start: 73419279
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73419280
feature_type: variation
id: rs756473256
seq_region_name: 17
source: dbSNP
start: 73419280
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419281
feature_type: variation
id: rs1599548209
seq_region_name: 17
source: dbSNP
start: 73419281
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419282
feature_type: variation
id: rs539853362
seq_region_name: 17
source: dbSNP
start: 73419282
strand: 1
-
alleles:
- GGGGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73419287
feature_type: variation
id: rs768348482
seq_region_name: 17
source: dbSNP
start: 73419282
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419283
feature_type: variation
id: rs2063208642
seq_region_name: 17
source: dbSNP
start: 73419283
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419285
feature_type: variation
id: rs757753465
seq_region_name: 17
source: dbSNP
start: 73419285
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419286
feature_type: variation
id: rs779252529
seq_region_name: 17
source: dbSNP
start: 73419286
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419287
feature_type: variation
id: rs374465306
seq_region_name: 17
source: dbSNP
start: 73419287
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419288
feature_type: variation
id: rs1285252701
seq_region_name: 17
source: dbSNP
start: 73419288
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419293
feature_type: variation
id: rs771422779
seq_region_name: 17
source: dbSNP
start: 73419293
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419294
feature_type: variation
id: rs779539793
seq_region_name: 17
source: dbSNP
start: 73419294
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73419300
feature_type: variation
id: rs1411593216
seq_region_name: 17
source: dbSNP
start: 73419300
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73419301
feature_type: variation
id: rs147914991
seq_region_name: 17
source: dbSNP
start: 73419301
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73419306
feature_type: variation
id: rs768351619
seq_region_name: 17
source: dbSNP
start: 73419306
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73419311
feature_type: variation
id: rs776386825
seq_region_name: 17
source: dbSNP
start: 73419311
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73419313
feature_type: variation
id: rs553180730
seq_region_name: 17
source: dbSNP
start: 73419313
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73419314
feature_type: variation
id: rs761551810
seq_region_name: 17
source: dbSNP
start: 73419314
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73419315
feature_type: variation
id: rs1451686280
seq_region_name: 17
source: dbSNP
start: 73419315
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73419317
feature_type: variation
id: rs1255811061
seq_region_name: 17
source: dbSNP
start: 73419317
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73419322
feature_type: variation
id: rs1437301359
seq_region_name: 17
source: dbSNP
start: 73419322
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73419323
feature_type: variation
id: rs1157339874
seq_region_name: 17
source: dbSNP
start: 73419323
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419325
feature_type: variation
id: rs1380192725
seq_region_name: 17
source: dbSNP
start: 73419325
strand: 1
-
alleles:
- CTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419331
feature_type: variation
id: rs1200196623
seq_region_name: 17
source: dbSNP
start: 73419328
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419330
feature_type: variation
id: rs769660826
seq_region_name: 17
source: dbSNP
start: 73419330
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419336
feature_type: variation
id: rs2063209183
seq_region_name: 17
source: dbSNP
start: 73419336
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419338
feature_type: variation
id: rs1214569001
seq_region_name: 17
source: dbSNP
start: 73419338
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419342
feature_type: variation
id: rs772972955
seq_region_name: 17
source: dbSNP
start: 73419342
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419344
feature_type: variation
id: rs762953630
seq_region_name: 17
source: dbSNP
start: 73419344
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419347
feature_type: variation
id: rs368689738
seq_region_name: 17
source: dbSNP
start: 73419347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419350
feature_type: variation
id: rs374080038
seq_region_name: 17
source: dbSNP
start: 73419350
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419352
feature_type: variation
id: rs1379149855
seq_region_name: 17
source: dbSNP
start: 73419352
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419355
feature_type: variation
id: rs752885234
seq_region_name: 17
source: dbSNP
start: 73419355
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419358
feature_type: variation
id: rs1287390125
seq_region_name: 17
source: dbSNP
start: 73419358
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419360
feature_type: variation
id: rs2063209391
seq_region_name: 17
source: dbSNP
start: 73419360
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419361
feature_type: variation
id: rs2063209407
seq_region_name: 17
source: dbSNP
start: 73419361
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419369
feature_type: variation
id: rs2063209426
seq_region_name: 17
source: dbSNP
start: 73419369
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419370
feature_type: variation
id: rs1195466913
seq_region_name: 17
source: dbSNP
start: 73419370
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419376
feature_type: variation
id: rs1351910601
seq_region_name: 17
source: dbSNP
start: 73419376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419381
feature_type: variation
id: rs2063209492
seq_region_name: 17
source: dbSNP
start: 73419381
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419382
feature_type: variation
id: rs1310344392
seq_region_name: 17
source: dbSNP
start: 73419382
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419384
feature_type: variation
id: rs2063209548
seq_region_name: 17
source: dbSNP
start: 73419384
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419386
feature_type: variation
id: rs546407115
seq_region_name: 17
source: dbSNP
start: 73419386
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419387
feature_type: variation
id: rs2063209597
seq_region_name: 17
source: dbSNP
start: 73419387
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419390
feature_type: variation
id: rs1432116614
seq_region_name: 17
source: dbSNP
start: 73419390
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419391
feature_type: variation
id: rs1379815643
seq_region_name: 17
source: dbSNP
start: 73419391
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419397
feature_type: variation
id: rs2063209676
seq_region_name: 17
source: dbSNP
start: 73419397
strand: 1
-
alleles:
- CTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419400
feature_type: variation
id: rs2063209705
seq_region_name: 17
source: dbSNP
start: 73419397
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419398
feature_type: variation
id: rs2063209733
seq_region_name: 17
source: dbSNP
start: 73419398
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419399
feature_type: variation
id: rs16977634
seq_region_name: 17
source: dbSNP
start: 73419399
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419402
feature_type: variation
id: rs1455764227
seq_region_name: 17
source: dbSNP
start: 73419402
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419406
feature_type: variation
id: rs2063209829
seq_region_name: 17
source: dbSNP
start: 73419406
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419409
feature_type: variation
id: rs528578657
seq_region_name: 17
source: dbSNP
start: 73419409
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419410
feature_type: variation
id: rs1599548326
seq_region_name: 17
source: dbSNP
start: 73419410
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419414
feature_type: variation
id: rs1160234560
seq_region_name: 17
source: dbSNP
start: 73419414
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419417
feature_type: variation
id: rs2063209909
seq_region_name: 17
source: dbSNP
start: 73419417
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419419
feature_type: variation
id: rs75493158
seq_region_name: 17
source: dbSNP
start: 73419419
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419428
feature_type: variation
id: rs1027303885
seq_region_name: 17
source: dbSNP
start: 73419428
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419429
feature_type: variation
id: rs1415891120
seq_region_name: 17
source: dbSNP
start: 73419429
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419439
feature_type: variation
id: rs2063210009
seq_region_name: 17
source: dbSNP
start: 73419439
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419442
feature_type: variation
id: rs2063210029
seq_region_name: 17
source: dbSNP
start: 73419442
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419447
feature_type: variation
id: rs2063210053
seq_region_name: 17
source: dbSNP
start: 73419447
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419453
feature_type: variation
id: rs2063210074
seq_region_name: 17
source: dbSNP
start: 73419453
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419455
feature_type: variation
id: rs1187297867
seq_region_name: 17
source: dbSNP
start: 73419455
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419456
feature_type: variation
id: rs1781484311
seq_region_name: 17
source: dbSNP
start: 73419456
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419460
feature_type: variation
id: rs972137730
seq_region_name: 17
source: dbSNP
start: 73419460
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419463
feature_type: variation
id: rs2063210158
seq_region_name: 17
source: dbSNP
start: 73419463
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419465
feature_type: variation
id: rs2063210182
seq_region_name: 17
source: dbSNP
start: 73419465
strand: 1
-
alleles:
- AAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419470
feature_type: variation
id: rs2063210199
seq_region_name: 17
source: dbSNP
start: 73419467
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419468
feature_type: variation
id: rs371302923
seq_region_name: 17
source: dbSNP
start: 73419468
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419470
feature_type: variation
id: rs529229997
seq_region_name: 17
source: dbSNP
start: 73419470
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419471
feature_type: variation
id: rs2063210238
seq_region_name: 17
source: dbSNP
start: 73419471
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419475
feature_type: variation
id: rs2063210257
seq_region_name: 17
source: dbSNP
start: 73419474
strand: 1
-
alleles:
- TATAATA
- TA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419481
feature_type: variation
id: rs1463196047
seq_region_name: 17
source: dbSNP
start: 73419475
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419480
feature_type: variation
id: rs981073836
seq_region_name: 17
source: dbSNP
start: 73419480
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419481
feature_type: variation
id: rs1208758854
seq_region_name: 17
source: dbSNP
start: 73419481
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419484
feature_type: variation
id: rs2063210341
seq_region_name: 17
source: dbSNP
start: 73419484
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419485
feature_type: variation
id: rs745789779
seq_region_name: 17
source: dbSNP
start: 73419485
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419486
feature_type: variation
id: rs2145579213
seq_region_name: 17
source: dbSNP
start: 73419486
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419487
feature_type: variation
id: rs542344263
seq_region_name: 17
source: dbSNP
start: 73419487
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419490
feature_type: variation
id: rs768371129
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73419626
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73419649
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419650
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419651
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419654
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419657
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419660
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419666
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419671
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419668
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419676
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73419680
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419682
feature_type: variation
id: rs1375397911
seq_region_name: 17
source: dbSNP
start: 73419682
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419687
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419687
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73419689
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419690
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seq_region_name: 17
source: dbSNP
start: 73419690
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419694
feature_type: variation
id: rs1451843397
seq_region_name: 17
source: dbSNP
start: 73419694
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419695
feature_type: variation
id: rs1268951440
seq_region_name: 17
source: dbSNP
start: 73419695
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419699
feature_type: variation
id: rs1568394537
seq_region_name: 17
source: dbSNP
start: 73419699
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419702
feature_type: variation
id: rs2063212250
seq_region_name: 17
source: dbSNP
start: 73419702
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419706
feature_type: variation
id: rs2063212279
seq_region_name: 17
source: dbSNP
start: 73419706
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419707
feature_type: variation
id: rs1202764564
seq_region_name: 17
source: dbSNP
start: 73419707
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419708
feature_type: variation
id: rs2063212329
seq_region_name: 17
source: dbSNP
start: 73419707
strand: 1
-
alleles:
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- AAAAAAAAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419715
feature_type: variation
id: rs1417558739
seq_region_name: 17
source: dbSNP
start: 73419708
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419709
feature_type: variation
id: rs2063212384
seq_region_name: 17
source: dbSNP
start: 73419709
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419711
feature_type: variation
id: rs2063212409
seq_region_name: 17
source: dbSNP
start: 73419711
strand: 1
-
alleles:
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- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419723
feature_type: variation
id: rs2063212432
seq_region_name: 17
source: dbSNP
start: 73419712
strand: 1
-
alleles:
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- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419722
feature_type: variation
id: rs1275331559
seq_region_name: 17
source: dbSNP
start: 73419713
strand: 1
-
alleles:
- AAACAACAAAAAAAACCCAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419733
feature_type: variation
id: rs1328261476
seq_region_name: 17
source: dbSNP
start: 73419713
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419714
feature_type: variation
id: rs1343004692
seq_region_name: 17
source: dbSNP
start: 73419714
strand: 1
-
alleles:
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- AA
- AACAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419721
feature_type: variation
id: rs1233990199
seq_region_name: 17
source: dbSNP
start: 73419714
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419715
feature_type: variation
id: rs1568394552
seq_region_name: 17
source: dbSNP
start: 73419715
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1333055989
seq_region_name: 17
source: dbSNP
start: 73419715
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419720
feature_type: variation
id: rs1286680753
seq_region_name: 17
source: dbSNP
start: 73419715
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419731
feature_type: variation
id: rs2063212572
seq_region_name: 17
source: dbSNP
start: 73419715
strand: 1
-
alleles:
- "-"
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419715
feature_type: variation
id: rs2063212599
seq_region_name: 17
source: dbSNP
start: 73419716
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419716
feature_type: variation
id: rs12946419
seq_region_name: 17
source: dbSNP
start: 73419716
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419716
feature_type: variation
id: rs1165312263
seq_region_name: 17
source: dbSNP
start: 73419716
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs772205582
seq_region_name: 17
source: dbSNP
start: 73419716
strand: 1
-
alleles:
- CAACAAAAAAAACCCAAAAAAACTCCCTCCTGGTGACTTGCACCTGTAATCCCAAATACCTGGGAGACTGAGGTGGGAGGATGGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTGTGTTTGCATCACGGAACTACAGCCTGGGAAACAGAGACCCTGTCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419879
feature_type: variation
id: rs2063212640
seq_region_name: 17
source: dbSNP
start: 73419716
strand: 1
-
alleles:
- AA
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419718
feature_type: variation
id: rs1568394574
seq_region_name: 17
source: dbSNP
start: 73419717
strand: 1
-
alleles:
- ACA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419720
feature_type: variation
id: rs1568394576
seq_region_name: 17
source: dbSNP
start: 73419718
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs12946420
seq_region_name: 17
source: dbSNP
start: 73419719
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs775551291
seq_region_name: 17
source: dbSNP
start: 73419719
strand: 1
-
alleles:
- CAAAAAAAACCCAAAAAAACTCCCTCCTGGTGACTTGCACCTGTAATCCCAAATACCTGGGAGACTGAGGTGGGAGGATGGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTGTGTTTGCATCACGGAACTACAGCCTGGGAAACAGAGACCCTGTCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419879
feature_type: variation
id: rs2063212763
seq_region_name: 17
source: dbSNP
start: 73419719
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419720
feature_type: variation
id: rs2063212784
seq_region_name: 17
source: dbSNP
start: 73419720
strand: 1
-
alleles:
- AAAAAAAA
- AAA
- AAAAAAA
- AAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419727
feature_type: variation
id: rs902970784
seq_region_name: 17
source: dbSNP
start: 73419720
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419721
feature_type: variation
id: rs1431058525
seq_region_name: 17
source: dbSNP
start: 73419721
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419721
feature_type: variation
id: rs1568394591
seq_region_name: 17
source: dbSNP
start: 73419722
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419722
feature_type: variation
id: rs1289946596
seq_region_name: 17
source: dbSNP
start: 73419722
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419723
feature_type: variation
id: rs1252228791
seq_region_name: 17
source: dbSNP
start: 73419723
strand: 1
-
alleles:
- AAAAACCCAAAAA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419735
feature_type: variation
id: rs1472169024
seq_region_name: 17
source: dbSNP
start: 73419723
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419724
feature_type: variation
id: rs1206300859
seq_region_name: 17
source: dbSNP
start: 73419724
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419724
feature_type: variation
id: rs1568394597
seq_region_name: 17
source: dbSNP
start: 73419725
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419725
feature_type: variation
id: rs2063212994
seq_region_name: 17
source: dbSNP
start: 73419725
strand: 1
-
alleles:
- AAACCCAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419733
feature_type: variation
id: rs1440648272
seq_region_name: 17
source: dbSNP
start: 73419725
strand: 1
-
alleles:
- AACCCAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419732
feature_type: variation
id: rs1364226595
seq_region_name: 17
source: dbSNP
start: 73419726
strand: 1
-
alleles:
- AACCCAAAAAAACTCCCTCCTGGTGACTTGCACCTGTAATCCCAAATACCTGGGAGACTGAGGTGGGAGGATGGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTGTGTTTGCATCACGGAACTACAGCCTGGGAAACAGAGACCCTGTCTCAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419881
feature_type: variation
id: rs2063213049
seq_region_name: 17
source: dbSNP
start: 73419726
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1347203492
seq_region_name: 17
source: dbSNP
start: 73419727
strand: 1
-
alleles:
- ACC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419729
feature_type: variation
id: rs2063213091
seq_region_name: 17
source: dbSNP
start: 73419727
strand: 1
-
alleles:
- ACCCA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419731
feature_type: variation
id: rs1216831853
seq_region_name: 17
source: dbSNP
start: 73419727
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419728
feature_type: variation
id: rs1351297129
seq_region_name: 17
source: dbSNP
start: 73419728
strand: 1
-
alleles:
- CCC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419730
feature_type: variation
id: rs55832839
seq_region_name: 17
source: dbSNP
start: 73419728
strand: 1
-
alleles:
- CCC
- C
- CCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419730
feature_type: variation
id: rs760930859
seq_region_name: 17
source: dbSNP
start: 73419728
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419729
feature_type: variation
id: rs1277830261
seq_region_name: 17
source: dbSNP
start: 73419729
strand: 1
-
alleles:
- CCA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419731
feature_type: variation
id: rs1290623208
seq_region_name: 17
source: dbSNP
start: 73419729
strand: 1
-
alleles:
- CCAAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419733
feature_type: variation
id: rs2063213179
seq_region_name: 17
source: dbSNP
start: 73419729
strand: 1
-
alleles:
- CCAAAAA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419735
feature_type: variation
id: rs2063213200
seq_region_name: 17
source: dbSNP
start: 73419729
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419730
feature_type: variation
id: rs1340403003
seq_region_name: 17
source: dbSNP
start: 73419730
strand: 1
-
alleles:
- CA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419731
feature_type: variation
id: rs2063213218
seq_region_name: 17
source: dbSNP
start: 73419730
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419731
feature_type: variation
id: rs1335652796
seq_region_name: 17
source: dbSNP
start: 73419731
strand: 1
-
alleles:
- AAAAAAA
- AAAAAA
- AAAAAAAA
- AAAAAAAAA
- AAAAAAAAAAA
- AAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419737
feature_type: variation
id: rs1335442338
seq_region_name: 17
source: dbSNP
start: 73419731
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419732
feature_type: variation
id: rs2063213340
seq_region_name: 17
source: dbSNP
start: 73419732
strand: 1
-
alleles:
- AAAAAA
- AAAAAAACAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419737
feature_type: variation
id: rs2063213360
seq_region_name: 17
source: dbSNP
start: 73419732
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419733
feature_type: variation
id: rs1234913889
seq_region_name: 17
source: dbSNP
start: 73419733
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419734
feature_type: variation
id: rs2063213407
seq_region_name: 17
source: dbSNP
start: 73419734
strand: 1
-
alleles:
- AAAA
- AAAAACAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419737
feature_type: variation
id: rs2145580012
seq_region_name: 17
source: dbSNP
start: 73419734
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419735
feature_type: variation
id: rs1456402741
seq_region_name: 17
source: dbSNP
start: 73419735
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419737
feature_type: variation
id: rs1412183081
seq_region_name: 17
source: dbSNP
start: 73419737
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419738
feature_type: variation
id: rs1287535406
seq_region_name: 17
source: dbSNP
start: 73419738
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419739
feature_type: variation
id: rs1320863495
seq_region_name: 17
source: dbSNP
start: 73419739
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419739
feature_type: variation
id: rs2145580061
seq_region_name: 17
source: dbSNP
start: 73419739
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419740
feature_type: variation
id: rs1178735886
seq_region_name: 17
source: dbSNP
start: 73419740
strand: 1
-
alleles:
- "-"
- AAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419741
feature_type: variation
id: rs2063213514
seq_region_name: 17
source: dbSNP
start: 73419742
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419742
feature_type: variation
id: rs566633531
seq_region_name: 17
source: dbSNP
start: 73419742
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419743
feature_type: variation
id: rs12451700
seq_region_name: 17
source: dbSNP
start: 73419743
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419743
feature_type: variation
id: rs2145580103
seq_region_name: 17
source: dbSNP
start: 73419743
strand: 1
-
alleles:
- CC
- CCCGCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419745
feature_type: variation
id: rs2063213595
seq_region_name: 17
source: dbSNP
start: 73419744
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419746
feature_type: variation
id: rs2145580115
seq_region_name: 17
source: dbSNP
start: 73419746
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419749
feature_type: variation
id: rs2145580119
seq_region_name: 17
source: dbSNP
start: 73419749
strand: 1
-
alleles:
- ACT
- ACTACT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419753
feature_type: variation
id: rs1599548766
seq_region_name: 17
source: dbSNP
start: 73419751
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419752
feature_type: variation
id: rs1188142643
seq_region_name: 17
source: dbSNP
start: 73419752
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419753
feature_type: variation
id: rs1599548774
seq_region_name: 17
source: dbSNP
start: 73419753
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419758
feature_type: variation
id: rs2063213947
seq_region_name: 17
source: dbSNP
start: 73419758
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419762
feature_type: variation
id: rs2063213969
seq_region_name: 17
source: dbSNP
start: 73419762
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419763
feature_type: variation
id: rs2063213986
seq_region_name: 17
source: dbSNP
start: 73419763
strand: 1
-
alleles:
- AAATACCTGGGA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419780
feature_type: variation
id: rs1599548783
seq_region_name: 17
source: dbSNP
start: 73419769
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419771
feature_type: variation
id: rs2063214035
seq_region_name: 17
source: dbSNP
start: 73419771
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419774
feature_type: variation
id: rs2063214057
seq_region_name: 17
source: dbSNP
start: 73419774
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419775
feature_type: variation
id: rs10852747
seq_region_name: 17
source: dbSNP
start: 73419775
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419776
feature_type: variation
id: rs2063214126
seq_region_name: 17
source: dbSNP
start: 73419776
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419784
feature_type: variation
id: rs2063214153
seq_region_name: 17
source: dbSNP
start: 73419784
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419788
feature_type: variation
id: rs1599548800
seq_region_name: 17
source: dbSNP
start: 73419788
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419789
feature_type: variation
id: rs2145580202
seq_region_name: 17
source: dbSNP
start: 73419789
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419790
feature_type: variation
id: rs889011005
seq_region_name: 17
source: dbSNP
start: 73419790
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419794
feature_type: variation
id: rs1208133574
seq_region_name: 17
source: dbSNP
start: 73419794
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419805
feature_type: variation
id: rs555424078
seq_region_name: 17
source: dbSNP
start: 73419805
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419806
feature_type: variation
id: rs10852748
seq_region_name: 17
source: dbSNP
start: 73419806
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419814
feature_type: variation
id: rs2063214296
seq_region_name: 17
source: dbSNP
start: 73419814
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419819
feature_type: variation
id: rs1356074062
seq_region_name: 17
source: dbSNP
start: 73419819
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419825
feature_type: variation
id: rs2063214348
seq_region_name: 17
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73419896
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419896
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73419897
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73419905
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419905
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419916
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419918
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419919
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419923
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419924
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1599549010
seq_region_name: 17
source: dbSNP
start: 73419924
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063215951
seq_region_name: 17
source: dbSNP
start: 73419927
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
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id: rs546370526
seq_region_name: 17
source: dbSNP
start: 73419929
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063215984
seq_region_name: 17
source: dbSNP
start: 73419930
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063215997
seq_region_name: 17
source: dbSNP
start: 73419931
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419934
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73419937
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419942
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73419943
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419946
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419947
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419947
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs78509441
seq_region_name: 17
source: dbSNP
start: 73419948
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs966767970
seq_region_name: 17
source: dbSNP
start: 73419950
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145580721
seq_region_name: 17
source: dbSNP
start: 73419954
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419965
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419970
feature_type: variation
id: rs2063216247
seq_region_name: 17
source: dbSNP
start: 73419970
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419974
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419974
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419975
feature_type: variation
id: rs2145580749
seq_region_name: 17
source: dbSNP
start: 73419975
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419977
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419977
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419987
feature_type: variation
id: rs1237488957
seq_region_name: 17
source: dbSNP
start: 73419987
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419988
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73419988
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419989
feature_type: variation
id: rs2063216357
seq_region_name: 17
source: dbSNP
start: 73419989
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419991
feature_type: variation
id: rs1418483665
seq_region_name: 17
source: dbSNP
start: 73419991
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419992
feature_type: variation
id: rs2063216405
seq_region_name: 17
source: dbSNP
start: 73419992
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419996
feature_type: variation
id: rs1158547955
seq_region_name: 17
source: dbSNP
start: 73419996
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73419998
feature_type: variation
id: rs925365512
seq_region_name: 17
source: dbSNP
start: 73419998
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420208
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alleles:
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assembly_name: GRCh38
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start: 73420209
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420214
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73420215
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73420219
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420223
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73420225
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420227
strand: 1
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420228
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420229
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420231
strand: 1
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alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420233
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420234
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420238
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73420239
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seq_region_name: 17
source: dbSNP
start: 73420239
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs902743571
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420370
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420371
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420378
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145581584
seq_region_name: 17
source: dbSNP
start: 73420383
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420388
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73420388
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420402
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420405
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420409
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420412
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1270867086
seq_region_name: 17
source: dbSNP
start: 73420413
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1162844533
seq_region_name: 17
source: dbSNP
start: 73420414
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420417
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420419
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420420
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1392615774
seq_region_name: 17
source: dbSNP
start: 73420424
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs908948467
seq_region_name: 17
source: dbSNP
start: 73420425
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs2063220009
seq_region_name: 17
source: dbSNP
start: 73420425
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420432
feature_type: variation
id: rs2063220027
seq_region_name: 17
source: dbSNP
start: 73420432
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063220048
seq_region_name: 17
source: dbSNP
start: 73420434
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420439
feature_type: variation
id: rs2063220066
seq_region_name: 17
source: dbSNP
start: 73420439
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420445
feature_type: variation
id: rs937805453
seq_region_name: 17
source: dbSNP
start: 73420445
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420450
feature_type: variation
id: rs2063220120
seq_region_name: 17
source: dbSNP
start: 73420450
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1300839007
seq_region_name: 17
source: dbSNP
start: 73420451
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1647331843
seq_region_name: 17
source: dbSNP
start: 73420454
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420455
feature_type: variation
id: rs1322789764
seq_region_name: 17
source: dbSNP
start: 73420455
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420456
feature_type: variation
id: rs1326534015
seq_region_name: 17
source: dbSNP
start: 73420456
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420458
feature_type: variation
id: rs2063220221
seq_region_name: 17
source: dbSNP
start: 73420458
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420459
feature_type: variation
id: rs1401245336
seq_region_name: 17
source: dbSNP
start: 73420459
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420463
feature_type: variation
id: rs1055181987
seq_region_name: 17
source: dbSNP
start: 73420463
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420463
feature_type: variation
id: rs1555766349
seq_region_name: 17
source: dbSNP
start: 73420464
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420464
feature_type: variation
id: rs896130904
seq_region_name: 17
source: dbSNP
start: 73420464
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420466
feature_type: variation
id: rs2063220328
seq_region_name: 17
source: dbSNP
start: 73420466
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420467
feature_type: variation
id: rs1347745895
seq_region_name: 17
source: dbSNP
start: 73420467
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73420469
feature_type: variation
id: rs1599549501
seq_region_name: 17
source: dbSNP
start: 73420469
strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420580
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420588
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420611
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73420616
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420616
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73420631
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73420641
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420652
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs555499980
seq_region_name: 17
source: dbSNP
start: 73420653
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1183872762
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420656
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs990793219
seq_region_name: 17
source: dbSNP
start: 73420658
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420659
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1242637869
seq_region_name: 17
source: dbSNP
start: 73420663
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420665
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420666
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1204324793
seq_region_name: 17
source: dbSNP
start: 73420669
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1325938575
seq_region_name: 17
source: dbSNP
start: 73420672
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420673
strand: 1
-
alleles:
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- CTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420674
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73420677
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73420678
feature_type: variation
id: rs2063221980
seq_region_name: 17
source: dbSNP
start: 73420678
strand: 1
-
alleles:
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- TT
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
- TCACTGCAACCTCCGTCTCCCGGGTTCA
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73420822
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73420824
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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start: 73420868
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420892
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420895
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73420906
strand: 1
-
alleles:
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alleles:
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alleles:
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73421026
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421031
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421038
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421043
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421044
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421045
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421046
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421049
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421050
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421059
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1234140561
seq_region_name: 17
source: dbSNP
start: 73421060
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73421066
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421067
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421069
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421072
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73421078
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421080
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421086
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421087
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421088
strand: 1
-
alleles:
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- CTCT
- CTCTCTCT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421088
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421091
strand: 1
-
alleles:
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- TGTTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421100
feature_type: variation
id: rs762698354
seq_region_name: 17
source: dbSNP
start: 73421093
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421094
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421096
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs376668833
seq_region_name: 17
source: dbSNP
start: 73421097
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421104
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421105
feature_type: variation
id: rs1363621118
seq_region_name: 17
source: dbSNP
start: 73421105
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421106
feature_type: variation
id: rs1160231688
seq_region_name: 17
source: dbSNP
start: 73421106
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421112
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421112
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421115
feature_type: variation
id: rs2063226227
seq_region_name: 17
source: dbSNP
start: 73421115
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421119
feature_type: variation
id: rs1421414589
seq_region_name: 17
source: dbSNP
start: 73421119
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421120
feature_type: variation
id: rs2145583159
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73421256
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73421262
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421278
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421287
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421290
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421297
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421322
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421327
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421328
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421329
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063228113
seq_region_name: 17
source: dbSNP
start: 73421331
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063228134
seq_region_name: 17
source: dbSNP
start: 73421336
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1425870923
seq_region_name: 17
source: dbSNP
start: 73421342
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421348
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seq_region_name: 17
source: dbSNP
start: 73421348
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063228196
seq_region_name: 17
source: dbSNP
start: 73421349
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73421350
strand: 1
-
alleles:
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- ATGATGAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421354
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id: rs1164498146
seq_region_name: 17
source: dbSNP
start: 73421350
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1310495165
seq_region_name: 17
source: dbSNP
start: 73421351
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421354
feature_type: variation
id: rs1372197406
seq_region_name: 17
source: dbSNP
start: 73421354
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421355
feature_type: variation
id: rs2063228291
seq_region_name: 17
source: dbSNP
start: 73421355
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421361
feature_type: variation
id: rs2063228312
seq_region_name: 17
source: dbSNP
start: 73421357
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73421456
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421480
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421482
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421483
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421485
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421489
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421492
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421494
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421499
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421499
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73421502
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421503
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421509
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421510
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063229885
seq_region_name: 17
source: dbSNP
start: 73421515
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063229911
seq_region_name: 17
source: dbSNP
start: 73421516
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73421519
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421519
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs371906064
seq_region_name: 17
source: dbSNP
start: 73421524
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1242807078
seq_region_name: 17
source: dbSNP
start: 73421525
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421527
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs373016785
seq_region_name: 17
source: dbSNP
start: 73421530
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421532
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421541
feature_type: variation
id: rs1444294000
seq_region_name: 17
source: dbSNP
start: 73421536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421537
feature_type: variation
id: rs2063230090
seq_region_name: 17
source: dbSNP
start: 73421537
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421538
feature_type: variation
id: rs999025786
seq_region_name: 17
source: dbSNP
start: 73421538
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421540
feature_type: variation
id: rs2063230130
seq_region_name: 17
source: dbSNP
start: 73421540
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421544
feature_type: variation
id: rs1023498003
seq_region_name: 17
source: dbSNP
start: 73421544
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73421571
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73421572
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1487887849
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421573
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- TTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063231049
seq_region_name: 17
source: dbSNP
start: 73421575
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1264698919
seq_region_name: 17
source: dbSNP
start: 73421575
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421577
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1030970009
seq_region_name: 17
source: dbSNP
start: 73421579
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063231186
seq_region_name: 17
source: dbSNP
start: 73421583
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599550534
seq_region_name: 17
source: dbSNP
start: 73421584
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1364818337
seq_region_name: 17
source: dbSNP
start: 73421587
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421592
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421595
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73421596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421597
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421597
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145584508
seq_region_name: 17
source: dbSNP
start: 73421598
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421600
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421601
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421604
feature_type: variation
id: rs1457475908
seq_region_name: 17
source: dbSNP
start: 73421604
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599550566
seq_region_name: 17
source: dbSNP
start: 73421607
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063231589
seq_region_name: 17
source: dbSNP
start: 73421608
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1197638411
seq_region_name: 17
source: dbSNP
start: 73421608
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599550569
seq_region_name: 17
source: dbSNP
start: 73421612
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1298954247
seq_region_name: 17
source: dbSNP
start: 73421614
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421618
feature_type: variation
id: rs2063231690
seq_region_name: 17
source: dbSNP
start: 73421618
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063231714
seq_region_name: 17
source: dbSNP
start: 73421626
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs565515236
seq_region_name: 17
source: dbSNP
start: 73421630
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421631
feature_type: variation
id: rs2063231758
seq_region_name: 17
source: dbSNP
start: 73421631
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063231785
seq_region_name: 17
source: dbSNP
start: 73421635
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs117702031
seq_region_name: 17
source: dbSNP
start: 73421637
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063231841
seq_region_name: 17
source: dbSNP
start: 73421638
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421640
feature_type: variation
id: rs989536468
seq_region_name: 17
source: dbSNP
start: 73421640
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421642
feature_type: variation
id: rs2145584621
seq_region_name: 17
source: dbSNP
start: 73421642
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421644
feature_type: variation
id: rs1398440594
seq_region_name: 17
source: dbSNP
start: 73421644
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs7405529
seq_region_name: 17
source: dbSNP
start: 73421646
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421654
feature_type: variation
id: rs2063231971
seq_region_name: 17
source: dbSNP
start: 73421654
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421657
feature_type: variation
id: rs2145584646
seq_region_name: 17
source: dbSNP
start: 73421657
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1318104500
seq_region_name: 17
source: dbSNP
start: 73421658
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421662
feature_type: variation
id: rs1279865415
seq_region_name: 17
source: dbSNP
start: 73421662
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599550598
seq_region_name: 17
source: dbSNP
start: 73421666
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421668
feature_type: variation
id: rs922531972
seq_region_name: 17
source: dbSNP
start: 73421668
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421669
feature_type: variation
id: rs7405531
seq_region_name: 17
source: dbSNP
start: 73421669
strand: 1
-
alleles:
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- ACAGGCGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421711
feature_type: variation
id: rs758937280
seq_region_name: 17
source: dbSNP
start: 73421669
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421671
feature_type: variation
id: rs2063232176
seq_region_name: 17
source: dbSNP
start: 73421671
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421676
feature_type: variation
id: rs2063232196
seq_region_name: 17
source: dbSNP
start: 73421676
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421677
feature_type: variation
id: rs1438756633
seq_region_name: 17
source: dbSNP
start: 73421677
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421680
feature_type: variation
id: rs1229774009
seq_region_name: 17
source: dbSNP
start: 73421680
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063232271
seq_region_name: 17
source: dbSNP
start: 73421682
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421684
feature_type: variation
id: rs2063232293
seq_region_name: 17
source: dbSNP
start: 73421684
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421686
feature_type: variation
id: rs1287644047
seq_region_name: 17
source: dbSNP
start: 73421686
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421687
feature_type: variation
id: rs537960045
seq_region_name: 17
source: dbSNP
start: 73421687
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421695
feature_type: variation
id: rs2063232415
seq_region_name: 17
source: dbSNP
start: 73421695
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421696
feature_type: variation
id: rs1217228015
seq_region_name: 17
source: dbSNP
start: 73421696
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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strand: 1
-
alleles:
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alleles:
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73421741
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063233345
seq_region_name: 17
source: dbSNP
start: 73421753
strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs940340702
seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73421802
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73421803
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421804
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421805
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs957793815
seq_region_name: 17
source: dbSNP
start: 73421807
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73421808
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063233760
seq_region_name: 17
source: dbSNP
start: 73421809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421810
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1011304809
seq_region_name: 17
source: dbSNP
start: 73421819
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs192861808
seq_region_name: 17
source: dbSNP
start: 73421824
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421826
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421827
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063233970
seq_region_name: 17
source: dbSNP
start: 73421829
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs976392100
seq_region_name: 17
source: dbSNP
start: 73421831
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063234034
seq_region_name: 17
source: dbSNP
start: 73421838
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1029525044
seq_region_name: 17
source: dbSNP
start: 73421839
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1240834998
seq_region_name: 17
source: dbSNP
start: 73421842
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs951326402
seq_region_name: 17
source: dbSNP
start: 73421843
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1379167225
seq_region_name: 17
source: dbSNP
start: 73421846
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1241023603
seq_region_name: 17
source: dbSNP
start: 73421846
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421847
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id: rs2063234162
seq_region_name: 17
source: dbSNP
start: 73421847
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421850
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs982559417
seq_region_name: 17
source: dbSNP
start: 73421851
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421857
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063234262
seq_region_name: 17
source: dbSNP
start: 73421858
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73421871
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599550835
seq_region_name: 17
source: dbSNP
start: 73421874
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421875
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1278895658
seq_region_name: 17
source: dbSNP
start: 73421876
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73421883
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs771884627
seq_region_name: 17
source: dbSNP
start: 73421887
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs909681071
seq_region_name: 17
source: dbSNP
start: 73421888
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1160434568
seq_region_name: 17
source: dbSNP
start: 73421890
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs550796566
seq_region_name: 17
source: dbSNP
start: 73421893
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421894
feature_type: variation
id: rs2063234469
seq_region_name: 17
source: dbSNP
start: 73421894
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421895
feature_type: variation
id: rs1403543824
seq_region_name: 17
source: dbSNP
start: 73421895
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421903
feature_type: variation
id: rs2063234522
seq_region_name: 17
source: dbSNP
start: 73421903
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421909
feature_type: variation
id: rs1422019157
seq_region_name: 17
source: dbSNP
start: 73421909
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421910
feature_type: variation
id: rs184792868
seq_region_name: 17
source: dbSNP
start: 73421910
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421911
feature_type: variation
id: rs1443633789
seq_region_name: 17
source: dbSNP
start: 73421911
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421913
feature_type: variation
id: rs114390066
seq_region_name: 17
source: dbSNP
start: 73421913
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73421916
feature_type: variation
id: rs1461124406
seq_region_name: 17
source: dbSNP
start: 73421916
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73422042
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73422052
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73422054
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73422057
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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start: 73422059
strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73422062
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73422064
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73422065
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73422066
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73422068
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422069
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422070
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422078
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422079
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422080
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422089
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568395977
seq_region_name: 17
source: dbSNP
start: 73422090
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422093
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422094
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422098
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422100
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422102
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422106
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422116
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73422121
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73422124
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063236728
seq_region_name: 17
source: dbSNP
start: 73422127
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063236753
seq_region_name: 17
source: dbSNP
start: 73422129
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422136
feature_type: variation
id: rs1258934244
seq_region_name: 17
source: dbSNP
start: 73422136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422137
feature_type: variation
id: rs8078868
seq_region_name: 17
source: dbSNP
start: 73422137
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422140
feature_type: variation
id: rs915972437
seq_region_name: 17
source: dbSNP
start: 73422140
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422142
feature_type: variation
id: rs2063236864
seq_region_name: 17
source: dbSNP
start: 73422142
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422143
feature_type: variation
id: rs8064874
seq_region_name: 17
source: dbSNP
start: 73422143
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422145
feature_type: variation
id: rs1004769988
seq_region_name: 17
source: dbSNP
start: 73422145
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422149
feature_type: variation
id: rs1234632097
seq_region_name: 17
source: dbSNP
start: 73422149
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422157
feature_type: variation
id: rs1599551106
seq_region_name: 17
source: dbSNP
start: 73422157
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422159
feature_type: variation
id: rs1015783252
seq_region_name: 17
source: dbSNP
start: 73422159
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422160
feature_type: variation
id: rs1302859196
seq_region_name: 17
source: dbSNP
start: 73422160
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422167
feature_type: variation
id: rs981423673
seq_region_name: 17
source: dbSNP
start: 73422167
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422168
feature_type: variation
id: rs2063237061
seq_region_name: 17
source: dbSNP
start: 73422168
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422171
feature_type: variation
id: rs924583444
seq_region_name: 17
source: dbSNP
start: 73422171
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422172
feature_type: variation
id: rs549963976
seq_region_name: 17
source: dbSNP
start: 73422172
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422174
feature_type: variation
id: rs2063237133
seq_region_name: 17
source: dbSNP
start: 73422174
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422175
feature_type: variation
id: rs2063237166
seq_region_name: 17
source: dbSNP
start: 73422175
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422180
feature_type: variation
id: rs542120475
seq_region_name: 17
source: dbSNP
start: 73422180
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422182
feature_type: variation
id: rs2145585799
seq_region_name: 17
source: dbSNP
start: 73422182
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422183
feature_type: variation
id: rs1055085845
seq_region_name: 17
source: dbSNP
start: 73422183
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422184
feature_type: variation
id: rs1331573588
seq_region_name: 17
source: dbSNP
start: 73422184
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422187
feature_type: variation
id: rs963260844
seq_region_name: 17
source: dbSNP
start: 73422187
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422188
feature_type: variation
id: rs2063237298
seq_region_name: 17
source: dbSNP
start: 73422188
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422191
feature_type: variation
id: rs1599551138
seq_region_name: 17
source: dbSNP
start: 73422191
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422192
feature_type: variation
id: rs2145585840
seq_region_name: 17
source: dbSNP
start: 73422192
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422199
feature_type: variation
id: rs571720518
seq_region_name: 17
source: dbSNP
start: 73422199
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422200
feature_type: variation
id: rs539137387
seq_region_name: 17
source: dbSNP
start: 73422200
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422203
feature_type: variation
id: rs943532136
seq_region_name: 17
source: dbSNP
start: 73422203
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422209
feature_type: variation
id: rs1599551147
seq_region_name: 17
source: dbSNP
start: 73422209
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422211
feature_type: variation
id: rs1478315793
seq_region_name: 17
source: dbSNP
start: 73422211
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422215
feature_type: variation
id: rs1379290748
seq_region_name: 17
source: dbSNP
start: 73422215
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422217
feature_type: variation
id: rs1179815306
seq_region_name: 17
source: dbSNP
start: 73422217
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422219
feature_type: variation
id: rs1039231666
seq_region_name: 17
source: dbSNP
start: 73422219
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422220
feature_type: variation
id: rs376716856
seq_region_name: 17
source: dbSNP
start: 73422220
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422221
feature_type: variation
id: rs899572963
seq_region_name: 17
source: dbSNP
start: 73422221
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422222
feature_type: variation
id: rs2063237615
seq_region_name: 17
source: dbSNP
start: 73422222
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422225
feature_type: variation
id: rs190093175
seq_region_name: 17
source: dbSNP
start: 73422225
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422226
feature_type: variation
id: rs373648764
seq_region_name: 17
source: dbSNP
start: 73422226
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422227
feature_type: variation
id: rs2145585902
seq_region_name: 17
source: dbSNP
start: 73422227
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422234
feature_type: variation
id: rs1029377916
seq_region_name: 17
source: dbSNP
start: 73422234
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422235
feature_type: variation
id: rs1347820772
seq_region_name: 17
source: dbSNP
start: 73422235
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422236
feature_type: variation
id: rs151276113
seq_region_name: 17
source: dbSNP
start: 73422236
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422237
feature_type: variation
id: rs2063237758
seq_region_name: 17
source: dbSNP
start: 73422237
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422238
feature_type: variation
id: rs1599551187
seq_region_name: 17
source: dbSNP
start: 73422238
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422239
feature_type: variation
id: rs1003884572
seq_region_name: 17
source: dbSNP
start: 73422239
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422240
feature_type: variation
id: rs113632690
seq_region_name: 17
source: dbSNP
start: 73422240
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422241
feature_type: variation
id: rs200043081
seq_region_name: 17
source: dbSNP
start: 73422241
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422244
feature_type: variation
id: rs1248158648
seq_region_name: 17
source: dbSNP
start: 73422244
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422250
feature_type: variation
id: rs1287464596
seq_region_name: 17
source: dbSNP
start: 73422250
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422252
feature_type: variation
id: rs754125280
seq_region_name: 17
source: dbSNP
start: 73422252
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422254
feature_type: variation
id: rs1204716429
seq_region_name: 17
source: dbSNP
start: 73422254
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422255
feature_type: variation
id: rs181581473
seq_region_name: 17
source: dbSNP
start: 73422255
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422256
feature_type: variation
id: rs371653885
seq_region_name: 17
source: dbSNP
start: 73422256
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422257
feature_type: variation
id: rs1177441531
seq_region_name: 17
source: dbSNP
start: 73422257
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422259
feature_type: variation
id: rs369891609
seq_region_name: 17
source: dbSNP
start: 73422259
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422260
feature_type: variation
id: rs759008710
seq_region_name: 17
source: dbSNP
start: 73422260
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422261
feature_type: variation
id: rs946584357
seq_region_name: 17
source: dbSNP
start: 73422261
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422263
feature_type: variation
id: rs779523362
seq_region_name: 17
source: dbSNP
start: 73422263
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422264
feature_type: variation
id: rs746570015
seq_region_name: 17
source: dbSNP
start: 73422264
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422265
feature_type: variation
id: rs768265358
seq_region_name: 17
source: dbSNP
start: 73422265
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422266
feature_type: variation
id: rs2063238257
seq_region_name: 17
source: dbSNP
start: 73422266
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422267
feature_type: variation
id: rs780783425
seq_region_name: 17
source: dbSNP
start: 73422267
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422269
feature_type: variation
id: rs1870691778
seq_region_name: 17
source: dbSNP
start: 73422269
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422270
feature_type: variation
id: rs747858673
seq_region_name: 17
source: dbSNP
start: 73422270
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422271
feature_type: variation
id: rs769409729
seq_region_name: 17
source: dbSNP
start: 73422271
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422272
feature_type: variation
id: rs773126656
seq_region_name: 17
source: dbSNP
start: 73422272
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422273
feature_type: variation
id: rs374055960
seq_region_name: 17
source: dbSNP
start: 73422273
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422274
feature_type: variation
id: rs971237398
seq_region_name: 17
source: dbSNP
start: 73422274
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422277
feature_type: variation
id: rs2063238464
seq_region_name: 17
source: dbSNP
start: 73422277
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73422281
feature_type: variation
id: rs771043612
seq_region_name: 17
source: dbSNP
start: 73422281
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73422285
feature_type: variation
id: rs996789322
seq_region_name: 17
source: dbSNP
start: 73422285
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422289
feature_type: variation
id: rs2145586106
seq_region_name: 17
source: dbSNP
start: 73422289
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73422291
feature_type: variation
id: rs140473608
seq_region_name: 17
source: dbSNP
start: 73422291
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422292
feature_type: variation
id: rs558735054
seq_region_name: 17
source: dbSNP
start: 73422292
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422293
feature_type: variation
id: rs764295267
seq_region_name: 17
source: dbSNP
start: 73422293
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422294
feature_type: variation
id: rs2063238657
seq_region_name: 17
source: dbSNP
start: 73422294
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422295
feature_type: variation
id: rs1279911895
seq_region_name: 17
source: dbSNP
start: 73422295
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422296
feature_type: variation
id: rs753953334
seq_region_name: 17
source: dbSNP
start: 73422296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422297
feature_type: variation
id: rs2063238737
seq_region_name: 17
source: dbSNP
start: 73422297
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422302
feature_type: variation
id: rs1599551290
seq_region_name: 17
source: dbSNP
start: 73422302
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422306
feature_type: variation
id: rs576951938
seq_region_name: 17
source: dbSNP
start: 73422306
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422308
feature_type: variation
id: rs1263141139
seq_region_name: 17
source: dbSNP
start: 73422308
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422313
feature_type: variation
id: rs765511276
seq_region_name: 17
source: dbSNP
start: 73422313
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422316
feature_type: variation
id: rs750856100
seq_region_name: 17
source: dbSNP
start: 73422316
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422319
feature_type: variation
id: rs2063238930
seq_region_name: 17
source: dbSNP
start: 73422319
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422321
feature_type: variation
id: rs376007378
seq_region_name: 17
source: dbSNP
start: 73422321
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422322
feature_type: variation
id: rs763374574
seq_region_name: 17
source: dbSNP
start: 73422322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422324
feature_type: variation
id: rs752089939
seq_region_name: 17
source: dbSNP
start: 73422324
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422330
feature_type: variation
id: rs754435436
seq_region_name: 17
source: dbSNP
start: 73422330
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422331
feature_type: variation
id: rs546930131
seq_region_name: 17
source: dbSNP
start: 73422331
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422337
feature_type: variation
id: rs1241684227
seq_region_name: 17
source: dbSNP
start: 73422337
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422339
feature_type: variation
id: rs990207168
seq_region_name: 17
source: dbSNP
start: 73422339
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422340
feature_type: variation
id: rs2063239189
seq_region_name: 17
source: dbSNP
start: 73422340
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422341
feature_type: variation
id: rs370624729
seq_region_name: 17
source: dbSNP
start: 73422341
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422342
feature_type: variation
id: rs755854278
seq_region_name: 17
source: dbSNP
start: 73422342
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422345
feature_type: variation
id: rs375622516
seq_region_name: 17
source: dbSNP
start: 73422345
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422347
feature_type: variation
id: rs749150010
seq_region_name: 17
source: dbSNP
start: 73422347
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422348
feature_type: variation
id: rs2063239305
seq_region_name: 17
source: dbSNP
start: 73422348
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73422349
feature_type: variation
id: rs2063239344
seq_region_name: 17
source: dbSNP
start: 73422349
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422353
feature_type: variation
id: rs943655957
seq_region_name: 17
source: dbSNP
start: 73422353
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422356
feature_type: variation
id: rs367622362
seq_region_name: 17
source: dbSNP
start: 73422356
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422357
feature_type: variation
id: rs371718789
seq_region_name: 17
source: dbSNP
start: 73422357
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422358
feature_type: variation
id: rs1299798836
seq_region_name: 17
source: dbSNP
start: 73422358
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422364
feature_type: variation
id: rs141747864
seq_region_name: 17
source: dbSNP
start: 73422364
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422366
feature_type: variation
id: rs1338146986
seq_region_name: 17
source: dbSNP
start: 73422366
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422367
feature_type: variation
id: rs2145586427
seq_region_name: 17
source: dbSNP
start: 73422367
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422368
feature_type: variation
id: rs2145586434
seq_region_name: 17
source: dbSNP
start: 73422368
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422371
feature_type: variation
id: rs745817676
seq_region_name: 17
source: dbSNP
start: 73422371
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422374
feature_type: variation
id: rs2063239628
seq_region_name: 17
source: dbSNP
start: 73422374
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422376
feature_type: variation
id: rs776834149
seq_region_name: 17
source: dbSNP
start: 73422376
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422378
feature_type: variation
id: rs1160592901
seq_region_name: 17
source: dbSNP
start: 73422378
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422379
feature_type: variation
id: rs1422798454
seq_region_name: 17
source: dbSNP
start: 73422379
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422381
feature_type: variation
id: rs1413395921
seq_region_name: 17
source: dbSNP
start: 73422381
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73422384
feature_type: variation
id: rs761925869
seq_region_name: 17
source: dbSNP
start: 73422384
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422391
feature_type: variation
id: rs1402226867
seq_region_name: 17
source: dbSNP
start: 73422391
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422395
feature_type: variation
id: rs563991505
seq_region_name: 17
source: dbSNP
start: 73422395
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422398
feature_type: variation
id: rs1277365799
seq_region_name: 17
source: dbSNP
start: 73422398
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422401
feature_type: variation
id: rs2063239928
seq_region_name: 17
source: dbSNP
start: 73422401
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422403
feature_type: variation
id: rs1473871921
seq_region_name: 17
source: dbSNP
start: 73422403
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422406
feature_type: variation
id: rs962913692
seq_region_name: 17
source: dbSNP
start: 73422406
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422408
feature_type: variation
id: rs1442340604
seq_region_name: 17
source: dbSNP
start: 73422408
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422409
feature_type: variation
id: rs773416894
seq_region_name: 17
source: dbSNP
start: 73422409
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422414
feature_type: variation
id: rs1265716067
seq_region_name: 17
source: dbSNP
start: 73422414
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422415
feature_type: variation
id: rs1487522025
seq_region_name: 17
source: dbSNP
start: 73422415
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422416
feature_type: variation
id: rs2063240122
seq_region_name: 17
source: dbSNP
start: 73422416
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422417
feature_type: variation
id: rs763261502
seq_region_name: 17
source: dbSNP
start: 73422417
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422420
feature_type: variation
id: rs1430205656
seq_region_name: 17
source: dbSNP
start: 73422420
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422422
feature_type: variation
id: rs766752337
seq_region_name: 17
source: dbSNP
start: 73422422
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422423
feature_type: variation
id: rs1170877760
seq_region_name: 17
source: dbSNP
start: 73422423
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73422424
feature_type: variation
id: rs770127208
seq_region_name: 17
source: dbSNP
start: 73422424
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73422426
feature_type: variation
id: rs776061207
seq_region_name: 17
source: dbSNP
start: 73422426
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422427
feature_type: variation
id: rs752005360
seq_region_name: 17
source: dbSNP
start: 73422427
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73422430
feature_type: variation
id: rs201621565
seq_region_name: 17
source: dbSNP
start: 73422430
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422431
feature_type: variation
id: rs1358336715
seq_region_name: 17
source: dbSNP
start: 73422431
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73422433
feature_type: variation
id: rs766923673
seq_region_name: 17
source: dbSNP
start: 73422433
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73422434
feature_type: variation
id: rs1303580981
seq_region_name: 17
source: dbSNP
start: 73422434
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_acceptor_variant
end: 73422436
feature_type: variation
id: rs2145586657
seq_region_name: 17
source: dbSNP
start: 73422436
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73422437
feature_type: variation
id: rs2063240492
seq_region_name: 17
source: dbSNP
start: 73422437
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73422440
feature_type: variation
id: rs1332443364
seq_region_name: 17
source: dbSNP
start: 73422440
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73422443
feature_type: variation
id: rs752302118
seq_region_name: 17
source: dbSNP
start: 73422443
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73422444
feature_type: variation
id: rs2063240566
seq_region_name: 17
source: dbSNP
start: 73422444
strand: 1
-
alleles:
- "-"
- ACAGTACAGTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73422446
feature_type: variation
id: rs1218221774
seq_region_name: 17
source: dbSNP
start: 73422447
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73422447
feature_type: variation
id: rs2063240608
seq_region_name: 17
source: dbSNP
start: 73422447
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73422450
feature_type: variation
id: rs1273732769
seq_region_name: 17
source: dbSNP
start: 73422450
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422453
feature_type: variation
id: rs755692530
seq_region_name: 17
source: dbSNP
start: 73422453
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422455
feature_type: variation
id: rs777444731
seq_region_name: 17
source: dbSNP
start: 73422455
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422456
feature_type: variation
id: rs201687227
seq_region_name: 17
source: dbSNP
start: 73422456
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422461
feature_type: variation
id: rs2063240707
seq_region_name: 17
source: dbSNP
start: 73422461
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422462
feature_type: variation
id: rs757065321
seq_region_name: 17
source: dbSNP
start: 73422462
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422463
feature_type: variation
id: rs1216311585
seq_region_name: 17
source: dbSNP
start: 73422463
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422466
feature_type: variation
id: rs9894213
seq_region_name: 17
source: dbSNP
start: 73422466
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422467
feature_type: variation
id: rs2063240868
seq_region_name: 17
source: dbSNP
start: 73422467
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422468
feature_type: variation
id: rs772190434
seq_region_name: 17
source: dbSNP
start: 73422468
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422469
feature_type: variation
id: rs368008668
seq_region_name: 17
source: dbSNP
start: 73422469
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422470
feature_type: variation
id: rs372219617
seq_region_name: 17
source: dbSNP
start: 73422470
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422474
feature_type: variation
id: rs1246142291
seq_region_name: 17
source: dbSNP
start: 73422474
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422476
feature_type: variation
id: rs748296766
seq_region_name: 17
source: dbSNP
start: 73422476
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422477
feature_type: variation
id: rs1217782459
seq_region_name: 17
source: dbSNP
start: 73422477
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422487
feature_type: variation
id: rs980417839
seq_region_name: 17
source: dbSNP
start: 73422487
strand: 1
-
alleles:
- CTTCTT
- CTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422494
feature_type: variation
id: rs927625576
seq_region_name: 17
source: dbSNP
start: 73422489
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422491
feature_type: variation
id: rs2063241096
seq_region_name: 17
source: dbSNP
start: 73422491
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422496
feature_type: variation
id: rs2063241116
seq_region_name: 17
source: dbSNP
start: 73422496
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422497
feature_type: variation
id: rs2063241151
seq_region_name: 17
source: dbSNP
start: 73422497
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422501
feature_type: variation
id: rs2063241176
seq_region_name: 17
source: dbSNP
start: 73422498
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422499
feature_type: variation
id: rs1285305643
seq_region_name: 17
source: dbSNP
start: 73422499
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422501
feature_type: variation
id: rs1012813964
seq_region_name: 17
source: dbSNP
start: 73422501
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422503
feature_type: variation
id: rs960700608
seq_region_name: 17
source: dbSNP
start: 73422503
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422505
feature_type: variation
id: rs767016574
seq_region_name: 17
source: dbSNP
start: 73422505
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422507
feature_type: variation
id: rs541432952
seq_region_name: 17
source: dbSNP
start: 73422507
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422510
feature_type: variation
id: rs1349395748
seq_region_name: 17
source: dbSNP
start: 73422510
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422513
feature_type: variation
id: rs2063241327
seq_region_name: 17
source: dbSNP
start: 73422513
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422514
feature_type: variation
id: rs1324217673
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-
alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422694
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1003132680
seq_region_name: 17
source: dbSNP
start: 73422696
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422705
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422707
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145587198
seq_region_name: 17
source: dbSNP
start: 73422708
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422710
feature_type: variation
id: rs1374811526
seq_region_name: 17
source: dbSNP
start: 73422710
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063242881
seq_region_name: 17
source: dbSNP
start: 73422714
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1035057937
seq_region_name: 17
source: dbSNP
start: 73422715
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs960398770
seq_region_name: 17
source: dbSNP
start: 73422719
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1447815242
seq_region_name: 17
source: dbSNP
start: 73422722
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063242977
seq_region_name: 17
source: dbSNP
start: 73422723
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs74699376
seq_region_name: 17
source: dbSNP
start: 73422730
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599551763
seq_region_name: 17
source: dbSNP
start: 73422733
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs752653915
seq_region_name: 17
source: dbSNP
start: 73422737
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422738
strand: 1
-
alleles:
- GCTGGGTGTGGTGGCTC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1313959705
seq_region_name: 17
source: dbSNP
start: 73422741
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422742
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1342613193
seq_region_name: 17
source: dbSNP
start: 73422744
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1178909140
seq_region_name: 17
source: dbSNP
start: 73422745
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1399413309
seq_region_name: 17
source: dbSNP
start: 73422747
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063243257
seq_region_name: 17
source: dbSNP
start: 73422748
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422749
feature_type: variation
id: rs1377960504
seq_region_name: 17
source: dbSNP
start: 73422749
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599551783
seq_region_name: 17
source: dbSNP
start: 73422761
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1244475020
seq_region_name: 17
source: dbSNP
start: 73422762
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422769
feature_type: variation
id: rs2063243323
seq_region_name: 17
source: dbSNP
start: 73422769
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422774
feature_type: variation
id: rs2063243354
seq_region_name: 17
source: dbSNP
start: 73422774
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422784
feature_type: variation
id: rs2063243379
seq_region_name: 17
source: dbSNP
start: 73422784
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422791
feature_type: variation
id: rs1314916972
seq_region_name: 17
source: dbSNP
start: 73422790
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422792
feature_type: variation
id: rs760144365
seq_region_name: 17
source: dbSNP
start: 73422792
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422793
feature_type: variation
id: rs1239599225
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source: dbSNP
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73422895
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422898
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063244420
seq_region_name: 17
source: dbSNP
start: 73422903
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422905
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063244473
seq_region_name: 17
source: dbSNP
start: 73422910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422912
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422913
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1011631254
seq_region_name: 17
source: dbSNP
start: 73422914
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422915
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422918
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs986683582
seq_region_name: 17
source: dbSNP
start: 73422919
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422921
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73422922
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422944
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422945
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422946
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422947
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422950
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422953
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422954
feature_type: variation
id: rs2063244872
seq_region_name: 17
source: dbSNP
start: 73422954
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063244897
seq_region_name: 17
source: dbSNP
start: 73422958
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063244923
seq_region_name: 17
source: dbSNP
start: 73422961
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422962
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1030532097
seq_region_name: 17
source: dbSNP
start: 73422968
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1279350166
seq_region_name: 17
source: dbSNP
start: 73422969
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs954985977
seq_region_name: 17
source: dbSNP
start: 73422970
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422972
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422974
feature_type: variation
id: rs940030597
seq_region_name: 17
source: dbSNP
start: 73422974
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599551910
seq_region_name: 17
source: dbSNP
start: 73422978
strand: 1
-
alleles:
- ATT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422983
feature_type: variation
id: rs2145587708
seq_region_name: 17
source: dbSNP
start: 73422981
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422982
feature_type: variation
id: rs2063245105
seq_region_name: 17
source: dbSNP
start: 73422982
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422983
feature_type: variation
id: rs1441003094
seq_region_name: 17
source: dbSNP
start: 73422983
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422985
feature_type: variation
id: rs983565133
seq_region_name: 17
source: dbSNP
start: 73422985
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73422987
feature_type: variation
id: rs1350106096
seq_region_name: 17
source: dbSNP
start: 73422987
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73422996
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1166906748
seq_region_name: 17
source: dbSNP
start: 73422998
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs908027212
seq_region_name: 17
source: dbSNP
start: 73422999
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063245315
seq_region_name: 17
source: dbSNP
start: 73423006
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1476705761
seq_region_name: 17
source: dbSNP
start: 73423010
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423011
feature_type: variation
id: rs1362693977
seq_region_name: 17
source: dbSNP
start: 73423011
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423015
feature_type: variation
id: rs942207274
seq_region_name: 17
source: dbSNP
start: 73423015
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs973814871
seq_region_name: 17
source: dbSNP
start: 73423016
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423017
feature_type: variation
id: rs919673708
seq_region_name: 17
source: dbSNP
start: 73423017
strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423023
feature_type: variation
id: rs948413747
seq_region_name: 17
source: dbSNP
start: 73423023
strand: 1
-
alleles:
- AATGAAT
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- AATGAATGAAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423031
feature_type: variation
id: rs1265363110
seq_region_name: 17
source: dbSNP
start: 73423025
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423028
feature_type: variation
id: rs372756294
seq_region_name: 17
source: dbSNP
start: 73423028
strand: 1
-
alleles:
- AAT
- AATGAATAAATAAAT
- AATGAATAAATAAATAAAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423031
feature_type: variation
id: rs1488961136
seq_region_name: 17
source: dbSNP
start: 73423029
strand: 1
-
alleles:
- AATAAA
- AATAAACAAATAAATAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423034
feature_type: variation
id: rs1555766916
seq_region_name: 17
source: dbSNP
start: 73423029
strand: 1
-
alleles:
- AATAAATAAATAAATAA
- AATAAATAAATAA
- AATAAATAAATAAATAAATAAATAA
- AATAAATAAATAAATAAATAAATAAATAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423045
feature_type: variation
id: rs1279187898
seq_region_name: 17
source: dbSNP
start: 73423029
strand: 1
-
alleles:
- AATAAATAAATAAATAATAAATAAATAAA
- AATAAATAAATAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423057
feature_type: variation
id: rs931406570
seq_region_name: 17
source: dbSNP
start: 73423029
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423032
feature_type: variation
id: rs796374652
seq_region_name: 17
source: dbSNP
start: 73423032
strand: 1
-
alleles:
- AAA
- AAACAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423034
feature_type: variation
id: rs2063245602
seq_region_name: 17
source: dbSNP
start: 73423032
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423033
feature_type: variation
id: rs1385722741
seq_region_name: 17
source: dbSNP
start: 73423033
strand: 1
-
alleles:
- AATAAAT
- AATAAATTAATAAAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423039
feature_type: variation
id: rs1329790658
seq_region_name: 17
source: dbSNP
start: 73423033
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423037
feature_type: variation
id: rs2063245687
seq_region_name: 17
source: dbSNP
start: 73423037
strand: 1
-
alleles:
- AATAAATAATAAATAA
- AATAAATAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423052
feature_type: variation
id: rs2063245719
seq_region_name: 17
source: dbSNP
start: 73423037
strand: 1
-
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423044
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73423045
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73423045
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73423048
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423060
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs7405952
seq_region_name: 17
source: dbSNP
start: 73423064
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1053035327
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423071
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423072
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1021057997
seq_region_name: 17
source: dbSNP
start: 73423075
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423078
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063246613
seq_region_name: 17
source: dbSNP
start: 73423081
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423083
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423094
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423096
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423099
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423100
strand: 1
-
alleles:
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- ATAAATAAATAAATAAATAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs202118046
seq_region_name: 17
source: dbSNP
start: 73423100
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423102
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1257925732
seq_region_name: 17
source: dbSNP
start: 73423103
strand: 1
-
alleles:
- AATAAATAAATAATAAATAAATA
- AATAAATAAATA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063246976
seq_region_name: 17
source: dbSNP
start: 73423103
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423105
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73423112
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1466438466
seq_region_name: 17
source: dbSNP
start: 73423113
strand: 1
-
alleles:
- AAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1396984908
seq_region_name: 17
source: dbSNP
start: 73423117
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063247148
seq_region_name: 17
source: dbSNP
start: 73423119
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063247187
seq_region_name: 17
source: dbSNP
start: 73423120
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1156861729
seq_region_name: 17
source: dbSNP
start: 73423124
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423126
feature_type: variation
id: rs1321167515
seq_region_name: 17
source: dbSNP
start: 73423126
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063247287
seq_region_name: 17
source: dbSNP
start: 73423128
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423130
feature_type: variation
id: rs1439393797
seq_region_name: 17
source: dbSNP
start: 73423130
strand: 1
-
alleles:
- TTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423136
feature_type: variation
id: rs2063247385
seq_region_name: 17
source: dbSNP
start: 73423133
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423137
feature_type: variation
id: rs1021708303
seq_region_name: 17
source: dbSNP
start: 73423137
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423142
feature_type: variation
id: rs1239009925
seq_region_name: 17
source: dbSNP
start: 73423142
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423143
feature_type: variation
id: rs7405626
seq_region_name: 17
source: dbSNP
start: 73423143
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423149
feature_type: variation
id: rs1238555953
seq_region_name: 17
source: dbSNP
start: 73423149
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423155
feature_type: variation
id: rs1459081001
seq_region_name: 17
source: dbSNP
start: 73423155
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423159
feature_type: variation
id: rs2063247624
seq_region_name: 17
source: dbSNP
start: 73423159
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423160
feature_type: variation
id: rs1441018662
seq_region_name: 17
source: dbSNP
start: 73423160
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423162
feature_type: variation
id: rs2063247673
seq_region_name: 17
source: dbSNP
start: 73423162
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423164
feature_type: variation
id: rs2063247696
seq_region_name: 17
source: dbSNP
start: 73423164
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423172
feature_type: variation
id: rs2063247725
seq_region_name: 17
source: dbSNP
start: 73423172
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423173
feature_type: variation
id: rs553089899
seq_region_name: 17
source: dbSNP
start: 73423173
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423176
feature_type: variation
id: rs1030311286
seq_region_name: 17
source: dbSNP
start: 73423176
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1347672997
seq_region_name: 17
source: dbSNP
start: 73423180
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423181
feature_type: variation
id: rs912469560
seq_region_name: 17
source: dbSNP
start: 73423181
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423183
feature_type: variation
id: rs1237306453
seq_region_name: 17
source: dbSNP
start: 73423183
strand: 1
-
alleles:
- GCG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423185
feature_type: variation
id: rs1939885242
seq_region_name: 17
source: dbSNP
start: 73423183
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423184
feature_type: variation
id: rs2345421
seq_region_name: 17
source: dbSNP
start: 73423184
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423185
feature_type: variation
id: rs1177821803
seq_region_name: 17
source: dbSNP
start: 73423185
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423189
feature_type: variation
id: rs1375514631
seq_region_name: 17
source: dbSNP
start: 73423189
strand: 1
-
alleles:
- TCTTTC
- TC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423196
feature_type: variation
id: rs1468573225
seq_region_name: 17
source: dbSNP
start: 73423191
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423196
feature_type: variation
id: rs1176245956
seq_region_name: 17
source: dbSNP
start: 73423196
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423199
feature_type: variation
id: rs1338504897
seq_region_name: 17
source: dbSNP
start: 73423199
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423200
feature_type: variation
id: rs1369273594
seq_region_name: 17
source: dbSNP
start: 73423200
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423201
feature_type: variation
id: rs1401469520
seq_region_name: 17
source: dbSNP
start: 73423201
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423206
feature_type: variation
id: rs983640544
seq_region_name: 17
source: dbSNP
start: 73423206
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423207
feature_type: variation
id: rs868317991
seq_region_name: 17
source: dbSNP
start: 73423207
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423209
feature_type: variation
id: rs2063248180
seq_region_name: 17
source: dbSNP
start: 73423209
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423215
feature_type: variation
id: rs1396545700
seq_region_name: 17
source: dbSNP
start: 73423215
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423217
feature_type: variation
id: rs1377194604
seq_region_name: 17
source: dbSNP
start: 73423217
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423219
feature_type: variation
id: rs2063248253
seq_region_name: 17
source: dbSNP
start: 73423219
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423226
feature_type: variation
id: rs1651898822
seq_region_name: 17
source: dbSNP
start: 73423226
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423231
feature_type: variation
id: rs2063248272
seq_region_name: 17
source: dbSNP
start: 73423227
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423237
feature_type: variation
id: rs2063248295
seq_region_name: 17
source: dbSNP
start: 73423237
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423239
feature_type: variation
id: rs1467692474
seq_region_name: 17
source: dbSNP
start: 73423239
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423243
feature_type: variation
id: rs1015599136
seq_region_name: 17
source: dbSNP
start: 73423243
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423244
feature_type: variation
id: rs972737757
seq_region_name: 17
source: dbSNP
start: 73423244
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423247
feature_type: variation
id: rs2077678876
seq_region_name: 17
source: dbSNP
start: 73423247
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423249
feature_type: variation
id: rs2063248417
seq_region_name: 17
source: dbSNP
start: 73423249
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423250
feature_type: variation
id: rs181964010
seq_region_name: 17
source: dbSNP
start: 73423250
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423251
feature_type: variation
id: rs931344569
seq_region_name: 17
source: dbSNP
start: 73423251
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423254
feature_type: variation
id: rs1188674756
seq_region_name: 17
source: dbSNP
start: 73423254
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423261
feature_type: variation
id: rs2063248489
seq_region_name: 17
source: dbSNP
start: 73423261
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423263
feature_type: variation
id: rs1599552228
seq_region_name: 17
source: dbSNP
start: 73423263
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423269
feature_type: variation
id: rs1599552233
seq_region_name: 17
source: dbSNP
start: 73423269
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423270
feature_type: variation
id: rs1372722316
seq_region_name: 17
source: dbSNP
start: 73423270
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423273
feature_type: variation
id: rs2063248582
seq_region_name: 17
source: dbSNP
start: 73423273
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423275
feature_type: variation
id: rs2063248610
seq_region_name: 17
source: dbSNP
start: 73423275
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423280
feature_type: variation
id: rs2063248637
seq_region_name: 17
source: dbSNP
start: 73423280
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423282
feature_type: variation
id: rs1387364154
seq_region_name: 17
source: dbSNP
start: 73423282
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423283
feature_type: variation
id: rs1044495159
seq_region_name: 17
source: dbSNP
start: 73423283
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423286
feature_type: variation
id: rs974021589
seq_region_name: 17
source: dbSNP
start: 73423286
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423287
feature_type: variation
id: rs927394024
seq_region_name: 17
source: dbSNP
start: 73423287
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423289
feature_type: variation
id: rs754579356
seq_region_name: 17
source: dbSNP
start: 73423289
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423289
feature_type: variation
id: rs2063248754
seq_region_name: 17
source: dbSNP
start: 73423289
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423291
feature_type: variation
id: rs1343941609
seq_region_name: 17
source: dbSNP
start: 73423291
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423294
feature_type: variation
id: rs919680672
seq_region_name: 17
source: dbSNP
start: 73423294
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423295
feature_type: variation
id: rs1353744064
seq_region_name: 17
source: dbSNP
start: 73423295
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423296
feature_type: variation
id: rs2063248865
seq_region_name: 17
source: dbSNP
start: 73423296
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423297
feature_type: variation
id: rs2063248891
seq_region_name: 17
source: dbSNP
start: 73423297
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423298
feature_type: variation
id: rs2145588710
seq_region_name: 17
source: dbSNP
start: 73423298
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423301
feature_type: variation
id: rs1283453733
seq_region_name: 17
source: dbSNP
start: 73423301
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423302
feature_type: variation
id: rs1599552281
seq_region_name: 17
source: dbSNP
start: 73423302
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423304
feature_type: variation
id: rs948482055
seq_region_name: 17
source: dbSNP
start: 73423304
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423306
feature_type: variation
id: rs1245231489
seq_region_name: 17
source: dbSNP
start: 73423306
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423307
feature_type: variation
id: rs562957923
seq_region_name: 17
source: dbSNP
start: 73423307
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423312
feature_type: variation
id: rs1276193046
seq_region_name: 17
source: dbSNP
start: 73423312
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423315
feature_type: variation
id: rs369682474
seq_region_name: 17
source: dbSNP
start: 73423315
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423317
feature_type: variation
id: rs1258521273
seq_region_name: 17
source: dbSNP
start: 73423317
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423321
feature_type: variation
id: rs2063249105
seq_region_name: 17
source: dbSNP
start: 73423321
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423324
feature_type: variation
id: rs2063249129
seq_region_name: 17
source: dbSNP
start: 73423324
strand: 1
-
alleles:
- TGACTCCTAAGTCCAAGCTTG
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423349
feature_type: variation
id: rs2063249156
seq_region_name: 17
source: dbSNP
start: 73423329
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423332
feature_type: variation
id: rs1399281498
seq_region_name: 17
source: dbSNP
start: 73423332
strand: 1
-
alleles:
- CTC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423334
feature_type: variation
id: rs2063249205
seq_region_name: 17
source: dbSNP
start: 73423332
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423333
feature_type: variation
id: rs2063249233
seq_region_name: 17
source: dbSNP
start: 73423333
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423334
feature_type: variation
id: rs2063249261
seq_region_name: 17
source: dbSNP
start: 73423334
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423336
feature_type: variation
id: rs2063249291
seq_region_name: 17
source: dbSNP
start: 73423336
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423336
feature_type: variation
id: rs2063249321
seq_region_name: 17
source: dbSNP
start: 73423336
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423339
feature_type: variation
id: rs2063249345
seq_region_name: 17
source: dbSNP
start: 73423339
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423344
feature_type: variation
id: rs1180389265
seq_region_name: 17
source: dbSNP
start: 73423343
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423344
feature_type: variation
id: rs1378373900
seq_region_name: 17
source: dbSNP
start: 73423344
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423347
feature_type: variation
id: rs574878448
seq_region_name: 17
source: dbSNP
start: 73423347
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423348
feature_type: variation
id: rs1356393225
seq_region_name: 17
source: dbSNP
start: 73423348
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423352
feature_type: variation
id: rs544122355
seq_region_name: 17
source: dbSNP
start: 73423352
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423353
feature_type: variation
id: rs780907784
seq_region_name: 17
source: dbSNP
start: 73423353
strand: 1
-
alleles:
- GGGAGGTGT
- GGGAGGTGTGGGAGGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423361
feature_type: variation
id: rs1222751530
seq_region_name: 17
source: dbSNP
start: 73423353
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423355
feature_type: variation
id: rs1390269698
seq_region_name: 17
source: dbSNP
start: 73423355
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423356
feature_type: variation
id: rs2063249603
seq_region_name: 17
source: dbSNP
start: 73423356
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423358
feature_type: variation
id: rs2063249630
seq_region_name: 17
source: dbSNP
start: 73423358
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423359
feature_type: variation
id: rs2063249660
seq_region_name: 17
source: dbSNP
start: 73423359
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423360
feature_type: variation
id: rs369151008
seq_region_name: 17
source: dbSNP
start: 73423360
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423361
feature_type: variation
id: rs1164247302
seq_region_name: 17
source: dbSNP
start: 73423361
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423364
feature_type: variation
id: rs565434960
seq_region_name: 17
source: dbSNP
start: 73423364
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423369
feature_type: variation
id: rs763176265
seq_region_name: 17
source: dbSNP
start: 73423369
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423371
feature_type: variation
id: rs1335786963
seq_region_name: 17
source: dbSNP
start: 73423371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423374
feature_type: variation
id: rs1448396766
seq_region_name: 17
source: dbSNP
start: 73423374
strand: 1
-
alleles:
- CGGG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423377
feature_type: variation
id: rs2063249838
seq_region_name: 17
source: dbSNP
start: 73423374
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423375
feature_type: variation
id: rs532801222
seq_region_name: 17
source: dbSNP
start: 73423375
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73423380
feature_type: variation
id: rs2063249901
seq_region_name: 17
source: dbSNP
start: 73423380
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423387
feature_type: variation
id: rs2063249927
seq_region_name: 17
source: dbSNP
start: 73423387
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73423388
feature_type: variation
id: rs372571803
seq_region_name: 17
source: dbSNP
start: 73423388
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423391
feature_type: variation
id: rs1240140306
seq_region_name: 17
source: dbSNP
start: 73423391
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423392
feature_type: variation
id: rs1266332848
seq_region_name: 17
source: dbSNP
start: 73423392
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423393
feature_type: variation
id: rs541270414
seq_region_name: 17
source: dbSNP
start: 73423393
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: stop_gained
end: 73423394
feature_type: variation
id: rs374663885
seq_region_name: 17
source: dbSNP
start: 73423394
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423396
feature_type: variation
id: rs1256460352
seq_region_name: 17
source: dbSNP
start: 73423396
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423402
feature_type: variation
id: rs2063250172
seq_region_name: 17
source: dbSNP
start: 73423402
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423407
feature_type: variation
id: rs753178072
seq_region_name: 17
source: dbSNP
start: 73423407
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423412
feature_type: variation
id: rs147076298
seq_region_name: 17
source: dbSNP
start: 73423412
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423413
feature_type: variation
id: rs1180565150
seq_region_name: 17
source: dbSNP
start: 73423413
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423414
feature_type: variation
id: rs1336718624
seq_region_name: 17
source: dbSNP
start: 73423414
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423416
feature_type: variation
id: rs138278077
seq_region_name: 17
source: dbSNP
start: 73423416
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423417
feature_type: variation
id: rs2145589069
seq_region_name: 17
source: dbSNP
start: 73423417
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73423418
feature_type: variation
id: rs1189474589
seq_region_name: 17
source: dbSNP
start: 73423418
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423419
feature_type: variation
id: rs2063250424
seq_region_name: 17
source: dbSNP
start: 73423419
strand: 1
-
alleles:
- GGGGG
- GGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73423423
feature_type: variation
id: rs761363502
seq_region_name: 17
source: dbSNP
start: 73423419
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423422
feature_type: variation
id: rs753479579
seq_region_name: 17
source: dbSNP
start: 73423422
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423423
feature_type: variation
id: rs2063250524
seq_region_name: 17
source: dbSNP
start: 73423423
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423427
feature_type: variation
id: rs1341047549
seq_region_name: 17
source: dbSNP
start: 73423427
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423435
feature_type: variation
id: rs1599552448
seq_region_name: 17
source: dbSNP
start: 73423435
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423440
feature_type: variation
id: rs745305768
seq_region_name: 17
source: dbSNP
start: 73423440
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423441
feature_type: variation
id: rs1369925576
seq_region_name: 17
source: dbSNP
start: 73423441
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423444
feature_type: variation
id: rs947231852
seq_region_name: 17
source: dbSNP
start: 73423444
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423449
feature_type: variation
id: rs2063250703
seq_region_name: 17
source: dbSNP
start: 73423449
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73423450
feature_type: variation
id: rs146912233
seq_region_name: 17
source: dbSNP
start: 73423450
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73423450
feature_type: variation
id: rs1238021298
seq_region_name: 17
source: dbSNP
start: 73423450
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423451
feature_type: variation
id: rs1162241644
seq_region_name: 17
source: dbSNP
start: 73423451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423453
feature_type: variation
id: rs1330783104
seq_region_name: 17
source: dbSNP
start: 73423453
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423455
feature_type: variation
id: rs2063250857
seq_region_name: 17
source: dbSNP
start: 73423455
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423456
feature_type: variation
id: rs2063250891
seq_region_name: 17
source: dbSNP
start: 73423456
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423459
feature_type: variation
id: rs77690040
seq_region_name: 17
source: dbSNP
start: 73423459
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423462
feature_type: variation
id: rs1463162271
seq_region_name: 17
source: dbSNP
start: 73423462
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423466
feature_type: variation
id: rs1466911865
seq_region_name: 17
source: dbSNP
start: 73423466
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73423467
feature_type: variation
id: rs750289259
seq_region_name: 17
source: dbSNP
start: 73423467
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423469
feature_type: variation
id: rs143406840
seq_region_name: 17
source: dbSNP
start: 73423469
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423470
feature_type: variation
id: rs1446623700
seq_region_name: 17
source: dbSNP
start: 73423470
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423473
feature_type: variation
id: rs779999339
seq_region_name: 17
source: dbSNP
start: 73423473
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423474
feature_type: variation
id: rs114085552
seq_region_name: 17
source: dbSNP
start: 73423474
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423476
feature_type: variation
id: rs35074489
seq_region_name: 17
source: dbSNP
start: 73423476
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423477
feature_type: variation
id: rs777834206
seq_region_name: 17
source: dbSNP
start: 73423477
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423479
feature_type: variation
id: rs1476740210
seq_region_name: 17
source: dbSNP
start: 73423479
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423480
feature_type: variation
id: rs2063251303
seq_region_name: 17
source: dbSNP
start: 73423480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423481
feature_type: variation
id: rs1245584442
seq_region_name: 17
source: dbSNP
start: 73423481
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423483
feature_type: variation
id: rs367803544
seq_region_name: 17
source: dbSNP
start: 73423483
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423484
feature_type: variation
id: rs1469487188
seq_region_name: 17
source: dbSNP
start: 73423484
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423485
feature_type: variation
id: rs1236207464
seq_region_name: 17
source: dbSNP
start: 73423485
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423486
feature_type: variation
id: rs2063251435
seq_region_name: 17
source: dbSNP
start: 73423486
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423493
feature_type: variation
id: rs973061139
seq_region_name: 17
source: dbSNP
start: 73423493
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423497
feature_type: variation
id: rs771193425
seq_region_name: 17
source: dbSNP
start: 73423497
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423498
feature_type: variation
id: rs2063251539
seq_region_name: 17
source: dbSNP
start: 73423498
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423499
feature_type: variation
id: rs1256164953
seq_region_name: 17
source: dbSNP
start: 73423499
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423501
feature_type: variation
id: rs1457383381
seq_region_name: 17
source: dbSNP
start: 73423501
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423503
feature_type: variation
id: rs774668096
seq_region_name: 17
source: dbSNP
start: 73423503
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423504
feature_type: variation
id: rs759856465
seq_region_name: 17
source: dbSNP
start: 73423504
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423507
feature_type: variation
id: rs190790569
seq_region_name: 17
source: dbSNP
start: 73423507
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423508
feature_type: variation
id: rs139146725
seq_region_name: 17
source: dbSNP
start: 73423508
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423509
feature_type: variation
id: rs1424155359
seq_region_name: 17
source: dbSNP
start: 73423509
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423510
feature_type: variation
id: rs371704241
seq_region_name: 17
source: dbSNP
start: 73423510
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423512
feature_type: variation
id: rs753615272
seq_region_name: 17
source: dbSNP
start: 73423512
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423515
feature_type: variation
id: rs753453005
seq_region_name: 17
source: dbSNP
start: 73423515
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73423521
feature_type: variation
id: rs534190960
seq_region_name: 17
source: dbSNP
start: 73423521
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73423522
feature_type: variation
id: rs2063251992
seq_region_name: 17
source: dbSNP
start: 73423522
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73423526
feature_type: variation
id: rs761531951
seq_region_name: 17
source: dbSNP
start: 73423526
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73423530
feature_type: variation
id: rs765018741
seq_region_name: 17
source: dbSNP
start: 73423530
strand: 1
-
alleles:
- ACAC
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73423537
feature_type: variation
id: rs766833907
seq_region_name: 17
source: dbSNP
start: 73423534
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73423535
feature_type: variation
id: rs369890852
seq_region_name: 17
source: dbSNP
start: 73423535
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73423536
feature_type: variation
id: rs758161865
seq_region_name: 17
source: dbSNP
start: 73423536
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73423537
feature_type: variation
id: rs534869778
seq_region_name: 17
source: dbSNP
start: 73423537
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73423538
feature_type: variation
id: rs200338601
seq_region_name: 17
source: dbSNP
start: 73423538
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423546
feature_type: variation
id: rs938781987
seq_region_name: 17
source: dbSNP
start: 73423546
strand: 1
-
alleles:
- ATCCCTAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423555
feature_type: variation
id: rs1235951438
seq_region_name: 17
source: dbSNP
start: 73423548
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423551
feature_type: variation
id: rs1220637477
seq_region_name: 17
source: dbSNP
start: 73423551
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423552
feature_type: variation
id: rs199798771
seq_region_name: 17
source: dbSNP
start: 73423552
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423554
feature_type: variation
id: rs368839366
seq_region_name: 17
source: dbSNP
start: 73423554
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423555
feature_type: variation
id: rs1480853947
seq_region_name: 17
source: dbSNP
start: 73423555
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423556
feature_type: variation
id: rs1234342249
seq_region_name: 17
source: dbSNP
start: 73423556
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423563
feature_type: variation
id: rs2063252376
seq_region_name: 17
source: dbSNP
start: 73423563
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423564
feature_type: variation
id: rs2145589634
seq_region_name: 17
source: dbSNP
start: 73423564
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423572
feature_type: variation
id: rs771031993
seq_region_name: 17
source: dbSNP
start: 73423572
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423575
feature_type: variation
id: rs776096418
seq_region_name: 17
source: dbSNP
start: 73423575
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423576
feature_type: variation
id: rs1441704671
seq_region_name: 17
source: dbSNP
start: 73423576
strand: 1
-
alleles:
- "-"
- TTGCGCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423576
feature_type: variation
id: rs2063252493
seq_region_name: 17
source: dbSNP
start: 73423577
strand: 1
-
alleles:
- "-"
- CCTGGGCGTTCAGTTCGTCGAGGTATTCCTTCGGCAGGTGCGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423579
feature_type: variation
id: rs2063252521
seq_region_name: 17
source: dbSNP
start: 73423580
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423580
feature_type: variation
id: rs2063252554
seq_region_name: 17
source: dbSNP
start: 73423580
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423581
feature_type: variation
id: rs2063252580
seq_region_name: 17
source: dbSNP
start: 73423581
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423582
feature_type: variation
id: rs1490035952
seq_region_name: 17
source: dbSNP
start: 73423582
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423587
feature_type: variation
id: rs2063252612
seq_region_name: 17
source: dbSNP
start: 73423587
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423605
feature_type: variation
id: rs2063252659
seq_region_name: 17
source: dbSNP
start: 73423605
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423606
feature_type: variation
id: rs913398050
seq_region_name: 17
source: dbSNP
start: 73423606
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423609
feature_type: variation
id: rs2063252714
seq_region_name: 17
source: dbSNP
start: 73423609
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423611
feature_type: variation
id: rs6501634
seq_region_name: 17
source: dbSNP
start: 73423611
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423617
feature_type: variation
id: rs181120333
seq_region_name: 17
source: dbSNP
start: 73423617
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423618
feature_type: variation
id: rs1224506926
seq_region_name: 17
source: dbSNP
start: 73423618
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423624
feature_type: variation
id: rs574940157
seq_region_name: 17
source: dbSNP
start: 73423624
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423625
feature_type: variation
id: rs913133572
seq_region_name: 17
source: dbSNP
start: 73423625
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423626
feature_type: variation
id: rs1718101811
seq_region_name: 17
source: dbSNP
start: 73423626
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423629
feature_type: variation
id: rs947315644
seq_region_name: 17
source: dbSNP
start: 73423629
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423630
feature_type: variation
id: rs1313007177
seq_region_name: 17
source: dbSNP
start: 73423630
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423632
feature_type: variation
id: rs2145589761
seq_region_name: 17
source: dbSNP
start: 73423632
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423633
feature_type: variation
id: rs2063252992
seq_region_name: 17
source: dbSNP
start: 73423633
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423636
feature_type: variation
id: rs867326339
seq_region_name: 17
source: dbSNP
start: 73423636
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423637
feature_type: variation
id: rs148828170
seq_region_name: 17
source: dbSNP
start: 73423637
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423639
feature_type: variation
id: rs1599552723
seq_region_name: 17
source: dbSNP
start: 73423639
strand: 1
-
alleles:
- AAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423642
feature_type: variation
id: rs2063253127
seq_region_name: 17
source: dbSNP
start: 73423639
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs889511946
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs557689241
seq_region_name: 17
source: dbSNP
start: 73423644
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145589798
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs143424739
seq_region_name: 17
source: dbSNP
start: 73423648
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs541676738
seq_region_name: 17
source: dbSNP
start: 73423649
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1383495696
seq_region_name: 17
source: dbSNP
start: 73423652
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs762298929
seq_region_name: 17
source: dbSNP
start: 73423653
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1472462065
seq_region_name: 17
source: dbSNP
start: 73423653
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs767577863
seq_region_name: 17
source: dbSNP
start: 73423658
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423660
feature_type: variation
id: rs1019402036
seq_region_name: 17
source: dbSNP
start: 73423660
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1258113782
seq_region_name: 17
source: dbSNP
start: 73423660
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063253406
seq_region_name: 17
source: dbSNP
start: 73423661
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1424043186
seq_region_name: 17
source: dbSNP
start: 73423664
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423665
feature_type: variation
id: rs2063253470
seq_region_name: 17
source: dbSNP
start: 73423665
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145589868
seq_region_name: 17
source: dbSNP
start: 73423671
strand: 1
-
alleles:
- TCTCTCT
- TCTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423681
feature_type: variation
id: rs2063253501
seq_region_name: 17
source: dbSNP
start: 73423675
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1285625699
seq_region_name: 17
source: dbSNP
start: 73423677
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1299036902
seq_region_name: 17
source: dbSNP
start: 73423680
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423682
feature_type: variation
id: rs1362627840
seq_region_name: 17
source: dbSNP
start: 73423682
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423686
feature_type: variation
id: rs1311113109
seq_region_name: 17
source: dbSNP
start: 73423686
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1356702510
seq_region_name: 17
source: dbSNP
start: 73423692
strand: 1
-
alleles:
- CCCTCCTGCTAAAGCCATCCTCACACCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423719
feature_type: variation
id: rs1428871404
seq_region_name: 17
source: dbSNP
start: 73423692
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423694
feature_type: variation
id: rs1288136268
seq_region_name: 17
source: dbSNP
start: 73423694
strand: 1
-
alleles:
- CCTGCTAAAGCCATCCTCACACCCCCCTGCT
- CCTGCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423726
feature_type: variation
id: rs1398640438
seq_region_name: 17
source: dbSNP
start: 73423696
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423699
feature_type: variation
id: rs921732373
seq_region_name: 17
source: dbSNP
start: 73423699
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423700
feature_type: variation
id: rs750662253
seq_region_name: 17
source: dbSNP
start: 73423700
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423708
feature_type: variation
id: rs1454050869
seq_region_name: 17
source: dbSNP
start: 73423708
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423711
feature_type: variation
id: rs8070326
seq_region_name: 17
source: dbSNP
start: 73423711
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423713
feature_type: variation
id: rs1162493659
seq_region_name: 17
source: dbSNP
start: 73423713
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423717
feature_type: variation
id: rs530298638
seq_region_name: 17
source: dbSNP
start: 73423717
strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423722
feature_type: variation
id: rs952629827
seq_region_name: 17
source: dbSNP
start: 73423717
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423718
feature_type: variation
id: rs1240173303
seq_region_name: 17
source: dbSNP
start: 73423718
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423719
feature_type: variation
id: rs890580318
seq_region_name: 17
source: dbSNP
start: 73423719
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423720
feature_type: variation
id: rs1287527841
seq_region_name: 17
source: dbSNP
start: 73423720
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423721
feature_type: variation
id: rs1487006320
seq_region_name: 17
source: dbSNP
start: 73423721
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423722
feature_type: variation
id: rs2063254132
seq_region_name: 17
source: dbSNP
start: 73423722
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423723
feature_type: variation
id: rs1004834428
seq_region_name: 17
source: dbSNP
start: 73423723
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423724
feature_type: variation
id: rs1034364246
seq_region_name: 17
source: dbSNP
start: 73423724
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423725
feature_type: variation
id: rs960117536
seq_region_name: 17
source: dbSNP
start: 73423725
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423727
feature_type: variation
id: rs2063254264
seq_region_name: 17
source: dbSNP
start: 73423727
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423732
feature_type: variation
id: rs1036801921
seq_region_name: 17
source: dbSNP
start: 73423732
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423732
feature_type: variation
id: rs2063254326
seq_region_name: 17
source: dbSNP
start: 73423732
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423733
feature_type: variation
id: rs899398986
seq_region_name: 17
source: dbSNP
start: 73423733
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423739
feature_type: variation
id: rs1185999422
seq_region_name: 17
source: dbSNP
start: 73423739
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423743
feature_type: variation
id: rs79065214
seq_region_name: 17
source: dbSNP
start: 73423743
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423744
feature_type: variation
id: rs1023895175
seq_region_name: 17
source: dbSNP
start: 73423744
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423745
feature_type: variation
id: rs6501635
seq_region_name: 17
source: dbSNP
start: 73423745
strand: 1
-
alleles:
- GAGAGA
- GAGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423756
feature_type: variation
id: rs1382279161
seq_region_name: 17
source: dbSNP
start: 73423751
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423753
feature_type: variation
id: rs2063254602
seq_region_name: 17
source: dbSNP
start: 73423753
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423760
feature_type: variation
id: rs978929903
seq_region_name: 17
source: dbSNP
start: 73423760
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423761
feature_type: variation
id: rs1003751449
seq_region_name: 17
source: dbSNP
start: 73423761
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423765
feature_type: variation
id: rs1035429634
seq_region_name: 17
source: dbSNP
start: 73423765
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423774
feature_type: variation
id: rs2063254711
seq_region_name: 17
source: dbSNP
start: 73423774
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423775
feature_type: variation
id: rs1683293227
seq_region_name: 17
source: dbSNP
start: 73423775
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423776
feature_type: variation
id: rs530996819
seq_region_name: 17
source: dbSNP
start: 73423776
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423777
feature_type: variation
id: rs1049358452
seq_region_name: 17
source: dbSNP
start: 73423777
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423779
feature_type: variation
id: rs1166743851
seq_region_name: 17
source: dbSNP
start: 73423779
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423781
feature_type: variation
id: rs889460432
seq_region_name: 17
source: dbSNP
start: 73423781
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423782
feature_type: variation
id: rs943756043
seq_region_name: 17
source: dbSNP
start: 73423782
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423783
feature_type: variation
id: rs2063254887
seq_region_name: 17
source: dbSNP
start: 73423783
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423786
feature_type: variation
id: rs2063254919
seq_region_name: 17
source: dbSNP
start: 73423786
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423788
feature_type: variation
id: rs552289839
seq_region_name: 17
source: dbSNP
start: 73423788
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423795
feature_type: variation
id: rs2063254973
seq_region_name: 17
source: dbSNP
start: 73423795
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423796
feature_type: variation
id: rs8070370
seq_region_name: 17
source: dbSNP
start: 73423796
strand: 1
-
alleles:
- CAGTTCAG
- CAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423808
feature_type: variation
id: rs2145590184
seq_region_name: 17
source: dbSNP
start: 73423801
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423803
feature_type: variation
id: rs896929847
seq_region_name: 17
source: dbSNP
start: 73423803
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423808
feature_type: variation
id: rs2063255068
seq_region_name: 17
source: dbSNP
start: 73423808
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423815
feature_type: variation
id: rs912865748
seq_region_name: 17
source: dbSNP
start: 73423815
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423816
feature_type: variation
id: rs73347744
seq_region_name: 17
source: dbSNP
start: 73423816
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423819
feature_type: variation
id: rs112527393
seq_region_name: 17
source: dbSNP
start: 73423819
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423820
feature_type: variation
id: rs2063255202
seq_region_name: 17
source: dbSNP
start: 73423820
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423826
feature_type: variation
id: rs979053431
seq_region_name: 17
source: dbSNP
start: 73423826
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423827
feature_type: variation
id: rs2063255259
seq_region_name: 17
source: dbSNP
start: 73423827
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423832
feature_type: variation
id: rs1599552952
seq_region_name: 17
source: dbSNP
start: 73423832
strand: 1
-
alleles:
- AAAAAA
- AAAA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423837
feature_type: variation
id: rs11287411
seq_region_name: 17
source: dbSNP
start: 73423832
strand: 1
-
alleles:
- AAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423838
feature_type: variation
id: rs1197126486
seq_region_name: 17
source: dbSNP
start: 73423836
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423837
feature_type: variation
id: rs1599552973
seq_region_name: 17
source: dbSNP
start: 73423837
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423844
feature_type: variation
id: rs1317884972
seq_region_name: 17
source: dbSNP
start: 73423844
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423845
feature_type: variation
id: rs921854917
seq_region_name: 17
source: dbSNP
start: 73423845
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423850
feature_type: variation
id: rs1599552981
seq_region_name: 17
source: dbSNP
start: 73423850
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423853
feature_type: variation
id: rs2063255521
seq_region_name: 17
source: dbSNP
start: 73423853
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423855
feature_type: variation
id: rs931815240
seq_region_name: 17
source: dbSNP
start: 73423855
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423857
feature_type: variation
id: rs1051582691
seq_region_name: 17
source: dbSNP
start: 73423857
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423859
feature_type: variation
id: rs2063255581
seq_region_name: 17
source: dbSNP
start: 73423859
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423862
feature_type: variation
id: rs8070503
seq_region_name: 17
source: dbSNP
start: 73423862
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423865
feature_type: variation
id: rs1308775315
seq_region_name: 17
source: dbSNP
start: 73423865
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423868
feature_type: variation
id: rs779059574
seq_region_name: 17
source: dbSNP
start: 73423868
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423871
feature_type: variation
id: rs201320246
seq_region_name: 17
source: dbSNP
start: 73423871
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423872
feature_type: variation
id: rs2145590365
seq_region_name: 17
source: dbSNP
start: 73423872
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423876
feature_type: variation
id: rs772417061
seq_region_name: 17
source: dbSNP
start: 73423876
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423878
feature_type: variation
id: rs1263555129
seq_region_name: 17
source: dbSNP
start: 73423878
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423880
feature_type: variation
id: rs1599553014
seq_region_name: 17
source: dbSNP
start: 73423880
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423882
feature_type: variation
id: rs370499803
seq_region_name: 17
source: dbSNP
start: 73423882
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423883
feature_type: variation
id: rs761226672
seq_region_name: 17
source: dbSNP
start: 73423883
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423884
feature_type: variation
id: rs1261979129
seq_region_name: 17
source: dbSNP
start: 73423884
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423885
feature_type: variation
id: rs2063255882
seq_region_name: 17
source: dbSNP
start: 73423885
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423886
feature_type: variation
id: rs769088840
seq_region_name: 17
source: dbSNP
start: 73423886
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423889
feature_type: variation
id: rs776246552
seq_region_name: 17
source: dbSNP
start: 73423889
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423890
feature_type: variation
id: rs761364572
seq_region_name: 17
source: dbSNP
start: 73423890
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423891
feature_type: variation
id: rs764861042
seq_region_name: 17
source: dbSNP
start: 73423891
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423892
feature_type: variation
id: rs772941489
seq_region_name: 17
source: dbSNP
start: 73423892
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423894
feature_type: variation
id: rs762516737
seq_region_name: 17
source: dbSNP
start: 73423894
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423895
feature_type: variation
id: rs751360271
seq_region_name: 17
source: dbSNP
start: 73423895
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423896
feature_type: variation
id: rs6501636
seq_region_name: 17
source: dbSNP
start: 73423896
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423897
feature_type: variation
id: rs1003699276
seq_region_name: 17
source: dbSNP
start: 73423897
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423905
feature_type: variation
id: rs1361521695
seq_region_name: 17
source: dbSNP
start: 73423903
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423904
feature_type: variation
id: rs1402281459
seq_region_name: 17
source: dbSNP
start: 73423904
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423905
feature_type: variation
id: rs745561692
seq_region_name: 17
source: dbSNP
start: 73423905
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73423906
feature_type: variation
id: rs767404435
seq_region_name: 17
source: dbSNP
start: 73423906
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73423911
feature_type: variation
id: rs752656016
seq_region_name: 17
source: dbSNP
start: 73423911
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423921
feature_type: variation
id: rs1870553606
seq_region_name: 17
source: dbSNP
start: 73423921
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423922
feature_type: variation
id: rs1387626922
seq_region_name: 17
source: dbSNP
start: 73423922
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73423923
feature_type: variation
id: rs892657172
seq_region_name: 17
source: dbSNP
start: 73423923
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423924
feature_type: variation
id: rs757273226
seq_region_name: 17
source: dbSNP
start: 73423924
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423926
feature_type: variation
id: rs1232375434
seq_region_name: 17
source: dbSNP
start: 73423926
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423927
feature_type: variation
id: rs778971620
seq_region_name: 17
source: dbSNP
start: 73423927
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423928
feature_type: variation
id: rs1599553095
seq_region_name: 17
source: dbSNP
start: 73423928
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423929
feature_type: variation
id: rs2063256488
seq_region_name: 17
source: dbSNP
start: 73423929
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423931
feature_type: variation
id: rs2145590606
seq_region_name: 17
source: dbSNP
start: 73423931
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423932
feature_type: variation
id: rs1355817633
seq_region_name: 17
source: dbSNP
start: 73423932
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423933
feature_type: variation
id: rs1214147862
seq_region_name: 17
source: dbSNP
start: 73423933
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423935
feature_type: variation
id: rs1437234506
seq_region_name: 17
source: dbSNP
start: 73423935
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73423937
feature_type: variation
id: rs142463427
seq_region_name: 17
source: dbSNP
start: 73423937
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73423938
feature_type: variation
id: rs780439807
seq_region_name: 17
source: dbSNP
start: 73423938
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423940
feature_type: variation
id: rs778093961
seq_region_name: 17
source: dbSNP
start: 73423940
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423942
feature_type: variation
id: rs769623208
seq_region_name: 17
source: dbSNP
start: 73423942
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423944
feature_type: variation
id: rs1192577031
seq_region_name: 17
source: dbSNP
start: 73423944
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423945
feature_type: variation
id: rs148009185
seq_region_name: 17
source: dbSNP
start: 73423945
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423955
feature_type: variation
id: rs1432119755
seq_region_name: 17
source: dbSNP
start: 73423955
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423956
feature_type: variation
id: rs769171123
seq_region_name: 17
source: dbSNP
start: 73423956
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423957
feature_type: variation
id: rs2063256832
seq_region_name: 17
source: dbSNP
start: 73423957
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423961
feature_type: variation
id: rs1253807942
seq_region_name: 17
source: dbSNP
start: 73423961
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423964
feature_type: variation
id: rs1599553153
seq_region_name: 17
source: dbSNP
start: 73423964
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423965
feature_type: variation
id: rs1381442123
seq_region_name: 17
source: dbSNP
start: 73423965
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423966
feature_type: variation
id: rs1422119764
seq_region_name: 17
source: dbSNP
start: 73423966
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73423967
feature_type: variation
id: rs777226549
seq_region_name: 17
source: dbSNP
start: 73423967
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423968
feature_type: variation
id: rs968751107
seq_region_name: 17
source: dbSNP
start: 73423968
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73423973
feature_type: variation
id: rs568863596
seq_region_name: 17
source: dbSNP
start: 73423973
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423974
feature_type: variation
id: rs1599553193
seq_region_name: 17
source: dbSNP
start: 73423974
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423978
feature_type: variation
id: rs769361190
seq_region_name: 17
source: dbSNP
start: 73423978
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423979
feature_type: variation
id: rs139580205
seq_region_name: 17
source: dbSNP
start: 73423979
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423981
feature_type: variation
id: rs762652962
seq_region_name: 17
source: dbSNP
start: 73423981
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423982
feature_type: variation
id: rs1310138435
seq_region_name: 17
source: dbSNP
start: 73423982
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423983
feature_type: variation
id: rs765987719
seq_region_name: 17
source: dbSNP
start: 73423983
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423984
feature_type: variation
id: rs375829412
seq_region_name: 17
source: dbSNP
start: 73423984
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423985
feature_type: variation
id: rs779683600
seq_region_name: 17
source: dbSNP
start: 73423985
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423986
feature_type: variation
id: rs1284964113
seq_region_name: 17
source: dbSNP
start: 73423986
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423988
feature_type: variation
id: rs759204082
seq_region_name: 17
source: dbSNP
start: 73423988
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423991
feature_type: variation
id: rs767314789
seq_region_name: 17
source: dbSNP
start: 73423991
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423993
feature_type: variation
id: rs539492511
seq_region_name: 17
source: dbSNP
start: 73423993
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73423994
feature_type: variation
id: rs1487979285
seq_region_name: 17
source: dbSNP
start: 73423994
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73423999
feature_type: variation
id: rs756114813
seq_region_name: 17
source: dbSNP
start: 73423999
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73424000
feature_type: variation
id: rs1239528340
seq_region_name: 17
source: dbSNP
start: 73424000
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424001
feature_type: variation
id: rs1442011243
seq_region_name: 17
source: dbSNP
start: 73424001
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424002
feature_type: variation
id: rs765291136
seq_region_name: 17
source: dbSNP
start: 73424002
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424003
feature_type: variation
id: rs557484583
seq_region_name: 17
source: dbSNP
start: 73424003
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424009
feature_type: variation
id: rs370368033
seq_region_name: 17
source: dbSNP
start: 73424009
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424010
feature_type: variation
id: rs2063257748
seq_region_name: 17
source: dbSNP
start: 73424010
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424011
feature_type: variation
id: rs2063257780
seq_region_name: 17
source: dbSNP
start: 73424011
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424012
feature_type: variation
id: rs1568397325
seq_region_name: 17
source: dbSNP
start: 73424012
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424013
feature_type: variation
id: rs200915505
seq_region_name: 17
source: dbSNP
start: 73424013
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424016
feature_type: variation
id: rs2063257838
seq_region_name: 17
source: dbSNP
start: 73424016
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424022
feature_type: variation
id: rs370432901
seq_region_name: 17
source: dbSNP
start: 73424022
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424023
feature_type: variation
id: rs1461173741
seq_region_name: 17
source: dbSNP
start: 73424023
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424024
feature_type: variation
id: rs1332121403
seq_region_name: 17
source: dbSNP
start: 73424024
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424025
feature_type: variation
id: rs1402554720
seq_region_name: 17
source: dbSNP
start: 73424025
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424027
feature_type: variation
id: rs920727081
seq_region_name: 17
source: dbSNP
start: 73424027
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424032
feature_type: variation
id: rs373457426
seq_region_name: 17
source: dbSNP
start: 73424032
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424034
feature_type: variation
id: rs75334660
seq_region_name: 17
source: dbSNP
start: 73424034
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: missense_variant
end: 73424036
feature_type: variation
id: rs35867741
seq_region_name: 17
source: dbSNP
start: 73424036
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73424037
feature_type: variation
id: rs748708401
seq_region_name: 17
source: dbSNP
start: 73424037
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424038
feature_type: variation
id: rs1214008736
seq_region_name: 17
source: dbSNP
start: 73424038
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424039
feature_type: variation
id: rs1795578492
seq_region_name: 17
source: dbSNP
start: 73424039
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424041
feature_type: variation
id: rs113489436
seq_region_name: 17
source: dbSNP
start: 73424041
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73424042
feature_type: variation
id: rs770497731
seq_region_name: 17
source: dbSNP
start: 73424042
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424043
feature_type: variation
id: rs2063258357
seq_region_name: 17
source: dbSNP
start: 73424043
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424050
feature_type: variation
id: rs773819582
seq_region_name: 17
source: dbSNP
start: 73424050
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424056
feature_type: variation
id: rs201431110
seq_region_name: 17
source: dbSNP
start: 73424056
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73424057
feature_type: variation
id: rs145662298
seq_region_name: 17
source: dbSNP
start: 73424057
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424059
feature_type: variation
id: rs760588176
seq_region_name: 17
source: dbSNP
start: 73424059
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424061
feature_type: variation
id: rs2063258568
seq_region_name: 17
source: dbSNP
start: 73424061
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424062
feature_type: variation
id: rs763974588
seq_region_name: 17
source: dbSNP
start: 73424062
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424065
feature_type: variation
id: rs1232777549
seq_region_name: 17
source: dbSNP
start: 73424065
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424066
feature_type: variation
id: rs1483892388
seq_region_name: 17
source: dbSNP
start: 73424066
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424068
feature_type: variation
id: rs746230163
seq_region_name: 17
source: dbSNP
start: 73424068
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424069
feature_type: variation
id: rs753841974
seq_region_name: 17
source: dbSNP
start: 73424069
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424070
feature_type: variation
id: rs1474965496
seq_region_name: 17
source: dbSNP
start: 73424070
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424072
feature_type: variation
id: rs2145591284
seq_region_name: 17
source: dbSNP
start: 73424072
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73424073
feature_type: variation
id: rs762889028
seq_region_name: 17
source: dbSNP
start: 73424073
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424074
feature_type: variation
id: rs766491720
seq_region_name: 17
source: dbSNP
start: 73424074
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424075
feature_type: variation
id: rs2063258914
seq_region_name: 17
source: dbSNP
start: 73424075
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424076
feature_type: variation
id: rs1464162399
seq_region_name: 17
source: dbSNP
start: 73424076
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424077
feature_type: variation
id: rs1302208418
seq_region_name: 17
source: dbSNP
start: 73424077
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424080
feature_type: variation
id: rs751663384
seq_region_name: 17
source: dbSNP
start: 73424080
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73424082
feature_type: variation
id: rs1359655167
seq_region_name: 17
source: dbSNP
start: 73424082
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424086
feature_type: variation
id: rs531038577
seq_region_name: 17
source: dbSNP
start: 73424086
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424088
feature_type: variation
id: rs1300864779
seq_region_name: 17
source: dbSNP
start: 73424088
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73424089
feature_type: variation
id: rs1354593084
seq_region_name: 17
source: dbSNP
start: 73424089
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73424092
feature_type: variation
id: rs1368404505
seq_region_name: 17
source: dbSNP
start: 73424092
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73424102
feature_type: variation
id: rs1020451011
seq_region_name: 17
source: dbSNP
start: 73424102
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73424103
feature_type: variation
id: rs1568397444
seq_region_name: 17
source: dbSNP
start: 73424103
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73424106
feature_type: variation
id: rs376706765
seq_region_name: 17
source: dbSNP
start: 73424106
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73424107
feature_type: variation
id: rs1279727611
seq_region_name: 17
source: dbSNP
start: 73424107
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73424109
feature_type: variation
id: rs371286803
seq_region_name: 17
source: dbSNP
start: 73424109
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424110
feature_type: variation
id: rs756579318
seq_region_name: 17
source: dbSNP
start: 73424110
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424111
feature_type: variation
id: rs778094931
seq_region_name: 17
source: dbSNP
start: 73424111
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424112
feature_type: variation
id: rs749817709
seq_region_name: 17
source: dbSNP
start: 73424112
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424113
feature_type: variation
id: rs1259086237
seq_region_name: 17
source: dbSNP
start: 73424113
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424114
feature_type: variation
id: rs374474344
seq_region_name: 17
source: dbSNP
start: 73424114
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424116
feature_type: variation
id: rs1446113666
seq_region_name: 17
source: dbSNP
start: 73424116
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424117
feature_type: variation
id: rs895762865
seq_region_name: 17
source: dbSNP
start: 73424117
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424120
feature_type: variation
id: rs1020304063
seq_region_name: 17
source: dbSNP
start: 73424120
strand: 1
-
alleles:
- AGAGGGAGAGG
- AGAGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424130
feature_type: variation
id: rs2145591462
seq_region_name: 17
source: dbSNP
start: 73424120
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424121
feature_type: variation
id: rs1272252926
seq_region_name: 17
source: dbSNP
start: 73424121
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424123
feature_type: variation
id: rs1485563729
seq_region_name: 17
source: dbSNP
start: 73424123
strand: 1
-
alleles:
- GGGAGAGGAAGGTACCTTGGGAG
- GGGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424145
feature_type: variation
id: rs2063259637
seq_region_name: 17
source: dbSNP
start: 73424123
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424125
feature_type: variation
id: rs778555388
seq_region_name: 17
source: dbSNP
start: 73424125
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424126
feature_type: variation
id: rs2063259682
seq_region_name: 17
source: dbSNP
start: 73424126
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424129
feature_type: variation
id: rs1265570956
seq_region_name: 17
source: dbSNP
start: 73424129
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424130
feature_type: variation
id: rs745503540
seq_region_name: 17
source: dbSNP
start: 73424130
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424131
feature_type: variation
id: rs771757602
seq_region_name: 17
source: dbSNP
start: 73424131
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424133
feature_type: variation
id: rs1656632060
seq_region_name: 17
source: dbSNP
start: 73424133
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424135
feature_type: variation
id: rs1426046825
seq_region_name: 17
source: dbSNP
start: 73424135
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424136
feature_type: variation
id: rs546893353
seq_region_name: 17
source: dbSNP
start: 73424136
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424138
feature_type: variation
id: rs1173893112
seq_region_name: 17
source: dbSNP
start: 73424138
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424139
feature_type: variation
id: rs2145591538
seq_region_name: 17
source: dbSNP
start: 73424139
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424142
feature_type: variation
id: rs563822762
seq_region_name: 17
source: dbSNP
start: 73424142
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424149
feature_type: variation
id: rs953537199
seq_region_name: 17
source: dbSNP
start: 73424149
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424157
feature_type: variation
id: rs2063259907
seq_region_name: 17
source: dbSNP
start: 73424157
strand: 1
-
alleles:
- TG
- TGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424158
feature_type: variation
id: rs2063259925
seq_region_name: 17
source: dbSNP
start: 73424157
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424158
feature_type: variation
id: rs1247363225
seq_region_name: 17
source: dbSNP
start: 73424158
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424162
feature_type: variation
id: rs769275141
seq_region_name: 17
source: dbSNP
start: 73424162
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424164
feature_type: variation
id: rs1394209395
seq_region_name: 17
source: dbSNP
start: 73424164
strand: 1
-
alleles:
- "-"
- GCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424165
feature_type: variation
id: rs1166097786
seq_region_name: 17
source: dbSNP
start: 73424166
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424167
feature_type: variation
id: rs2145591591
seq_region_name: 17
source: dbSNP
start: 73424167
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424168
feature_type: variation
id: rs2063260136
seq_region_name: 17
source: dbSNP
start: 73424168
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424169
feature_type: variation
id: rs575669866
seq_region_name: 17
source: dbSNP
start: 73424169
strand: 1
-
alleles:
- CGAGA
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424173
feature_type: variation
id: rs1463529057
seq_region_name: 17
source: dbSNP
start: 73424169
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424170
feature_type: variation
id: rs2063260210
seq_region_name: 17
source: dbSNP
start: 73424170
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424172
feature_type: variation
id: rs2063260238
seq_region_name: 17
source: dbSNP
start: 73424172
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424177
feature_type: variation
id: rs1165689520
seq_region_name: 17
source: dbSNP
start: 73424177
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424182
feature_type: variation
id: rs1474811341
seq_region_name: 17
source: dbSNP
start: 73424182
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424187
feature_type: variation
id: rs986288768
seq_region_name: 17
source: dbSNP
start: 73424187
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424188
feature_type: variation
id: rs962180884
seq_region_name: 17
source: dbSNP
start: 73424188
strand: 1
-
alleles:
- GGCAGAGGACAACTGCAGGCAACAGCCAGGCAG
- GGCAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424223
feature_type: variation
id: rs1466813148
seq_region_name: 17
source: dbSNP
start: 73424191
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424196
feature_type: variation
id: rs2063260419
seq_region_name: 17
source: dbSNP
start: 73424196
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424197
feature_type: variation
id: rs912110171
seq_region_name: 17
source: dbSNP
start: 73424197
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424201
feature_type: variation
id: rs1214079555
seq_region_name: 17
source: dbSNP
start: 73424201
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424202
feature_type: variation
id: rs2063260524
seq_region_name: 17
source: dbSNP
start: 73424202
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424203
feature_type: variation
id: rs2063260553
seq_region_name: 17
source: dbSNP
start: 73424203
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424209
feature_type: variation
id: rs971955032
seq_region_name: 17
source: dbSNP
start: 73424209
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424210
feature_type: variation
id: rs2063260614
seq_region_name: 17
source: dbSNP
start: 73424210
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424214
feature_type: variation
id: rs774937938
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs2063260678
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
start: 73424221
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063260705
seq_region_name: 17
source: dbSNP
start: 73424225
strand: 1
-
alleles:
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assembly_name: GRCh38
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id: rs762018049
seq_region_name: 17
source: dbSNP
start: 73424226
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73424229
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs141708953
seq_region_name: 17
source: dbSNP
start: 73424232
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs372898024
seq_region_name: 17
source: dbSNP
start: 73424235
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1056691708
seq_region_name: 17
source: dbSNP
start: 73424236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1443524883
seq_region_name: 17
source: dbSNP
start: 73424239
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063260909
seq_region_name: 17
source: dbSNP
start: 73424241
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs138698708
seq_region_name: 17
source: dbSNP
start: 73424242
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1323720801
seq_region_name: 17
source: dbSNP
start: 73424243
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063260958
seq_region_name: 17
source: dbSNP
start: 73424243
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1366859776
seq_region_name: 17
source: dbSNP
start: 73424252
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145591793
seq_region_name: 17
source: dbSNP
start: 73424257
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145591800
seq_region_name: 17
source: dbSNP
start: 73424261
strand: 1
-
alleles:
- AAA
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063261021
seq_region_name: 17
source: dbSNP
start: 73424261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1169140319
seq_region_name: 17
source: dbSNP
start: 73424262
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs6501637
seq_region_name: 17
source: dbSNP
start: 73424263
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063261129
seq_region_name: 17
source: dbSNP
start: 73424264
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063261153
seq_region_name: 17
source: dbSNP
start: 73424265
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1282188157
seq_region_name: 17
source: dbSNP
start: 73424266
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1345307463
seq_region_name: 17
source: dbSNP
start: 73424271
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs909666143
seq_region_name: 17
source: dbSNP
start: 73424272
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1959813744
seq_region_name: 17
source: dbSNP
start: 73424275
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063261281
seq_region_name: 17
source: dbSNP
start: 73424280
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1219554650
seq_region_name: 17
source: dbSNP
start: 73424281
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1272279448
seq_region_name: 17
source: dbSNP
start: 73424288
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063261363
seq_region_name: 17
source: dbSNP
start: 73424289
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063261393
seq_region_name: 17
source: dbSNP
start: 73424290
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063261424
seq_region_name: 17
source: dbSNP
start: 73424292
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1438316835
seq_region_name: 17
source: dbSNP
start: 73424296
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599553630
seq_region_name: 17
source: dbSNP
start: 73424297
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424299
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs766652568
seq_region_name: 17
source: dbSNP
start: 73424300
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs937145635
seq_region_name: 17
source: dbSNP
start: 73424302
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs561637980
seq_region_name: 17
source: dbSNP
start: 73424303
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063261586
seq_region_name: 17
source: dbSNP
start: 73424307
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs776677192
seq_region_name: 17
source: dbSNP
start: 73424309
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145591956
seq_region_name: 17
source: dbSNP
start: 73424313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs759623458
seq_region_name: 17
source: dbSNP
start: 73424315
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1279270136
seq_region_name: 17
source: dbSNP
start: 73424316
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs111715556
seq_region_name: 17
source: dbSNP
start: 73424319
strand: 1
-
alleles:
- G
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- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs529110532
seq_region_name: 17
source: dbSNP
start: 73424320
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424321
feature_type: variation
id: rs866351801
seq_region_name: 17
source: dbSNP
start: 73424321
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424323
feature_type: variation
id: rs2063261700
seq_region_name: 17
source: dbSNP
start: 73424323
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424327
feature_type: variation
id: rs1220578346
seq_region_name: 17
source: dbSNP
start: 73424327
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424334
feature_type: variation
id: rs1599553667
seq_region_name: 17
source: dbSNP
start: 73424334
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1330369453
seq_region_name: 17
source: dbSNP
start: 73424336
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424339
feature_type: variation
id: rs888750215
seq_region_name: 17
source: dbSNP
start: 73424339
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424340
feature_type: variation
id: rs1008554801
seq_region_name: 17
source: dbSNP
start: 73424340
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1173905160
seq_region_name: 17
source: dbSNP
start: 73424343
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424353
feature_type: variation
id: rs1455250841
seq_region_name: 17
source: dbSNP
start: 73424353
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424358
feature_type: variation
id: rs2063261892
seq_region_name: 17
source: dbSNP
start: 73424358
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424361
feature_type: variation
id: rs1488501778
seq_region_name: 17
source: dbSNP
start: 73424361
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424362
feature_type: variation
id: rs2145592073
seq_region_name: 17
source: dbSNP
start: 73424362
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424363
feature_type: variation
id: rs2063261962
seq_region_name: 17
source: dbSNP
start: 73424363
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424365
feature_type: variation
id: rs2063261997
seq_region_name: 17
source: dbSNP
start: 73424365
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424366
feature_type: variation
id: rs7214866
seq_region_name: 17
source: dbSNP
start: 73424366
strand: 1
-
alleles:
- AAA
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424368
feature_type: variation
id: rs1599553697
seq_region_name: 17
source: dbSNP
start: 73424366
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424370
feature_type: variation
id: rs751541784
seq_region_name: 17
source: dbSNP
start: 73424370
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424371
feature_type: variation
id: rs962014880
seq_region_name: 17
source: dbSNP
start: 73424371
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424375
feature_type: variation
id: rs2145592122
seq_region_name: 17
source: dbSNP
start: 73424375
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424377
feature_type: variation
id: rs993717476
seq_region_name: 17
source: dbSNP
start: 73424377
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424381
feature_type: variation
id: rs2063262294
seq_region_name: 17
source: dbSNP
start: 73424381
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424382
feature_type: variation
id: rs1475065098
seq_region_name: 17
source: dbSNP
start: 73424382
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424384
feature_type: variation
id: rs2063262350
seq_region_name: 17
source: dbSNP
start: 73424384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424386
feature_type: variation
id: rs1027465544
seq_region_name: 17
source: dbSNP
start: 73424386
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424390
feature_type: variation
id: rs1281053737
seq_region_name: 17
source: dbSNP
start: 73424390
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424391
feature_type: variation
id: rs2063262426
seq_region_name: 17
source: dbSNP
start: 73424391
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424392
feature_type: variation
id: rs569000991
seq_region_name: 17
source: dbSNP
start: 73424392
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424393
feature_type: variation
id: rs569162793
seq_region_name: 17
source: dbSNP
start: 73424393
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424397
feature_type: variation
id: rs114867088
seq_region_name: 17
source: dbSNP
start: 73424397
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424398
feature_type: variation
id: rs551435767
seq_region_name: 17
source: dbSNP
start: 73424398
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424399
feature_type: variation
id: rs1308975821
seq_region_name: 17
source: dbSNP
start: 73424399
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424402
feature_type: variation
id: rs1599553738
seq_region_name: 17
source: dbSNP
start: 73424402
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424413
feature_type: variation
id: rs7214999
seq_region_name: 17
source: dbSNP
start: 73424413
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424415
feature_type: variation
id: rs1292016258
seq_region_name: 17
source: dbSNP
start: 73424415
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424416
feature_type: variation
id: rs2145592221
seq_region_name: 17
source: dbSNP
start: 73424416
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424417
feature_type: variation
id: rs1599553755
seq_region_name: 17
source: dbSNP
start: 73424417
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424418
feature_type: variation
id: rs953485425
seq_region_name: 17
source: dbSNP
start: 73424418
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424426
feature_type: variation
id: rs533764016
seq_region_name: 17
source: dbSNP
start: 73424426
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424429
feature_type: variation
id: rs2063262703
seq_region_name: 17
source: dbSNP
start: 73424429
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424429
feature_type: variation
id: rs2063262726
seq_region_name: 17
source: dbSNP
start: 73424429
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424430
feature_type: variation
id: rs750228950
seq_region_name: 17
source: dbSNP
start: 73424430
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73424581
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424585
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73424588
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424599
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424601
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424605
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424609
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063264470
seq_region_name: 17
source: dbSNP
start: 73424611
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424612
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424616
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424617
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs897501778
seq_region_name: 17
source: dbSNP
start: 73424620
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424622
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063264601
seq_region_name: 17
source: dbSNP
start: 73424632
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1295248414
seq_region_name: 17
source: dbSNP
start: 73424633
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063264657
seq_region_name: 17
source: dbSNP
start: 73424634
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424636
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1000132543
seq_region_name: 17
source: dbSNP
start: 73424642
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs748666478
seq_region_name: 17
source: dbSNP
start: 73424643
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424650
feature_type: variation
id: rs1244820617
seq_region_name: 17
source: dbSNP
start: 73424650
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424652
feature_type: variation
id: rs2063264764
seq_region_name: 17
source: dbSNP
start: 73424652
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424654
feature_type: variation
id: rs2063264788
seq_region_name: 17
source: dbSNP
start: 73424654
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424655
feature_type: variation
id: rs1442250704
seq_region_name: 17
source: dbSNP
start: 73424655
strand: 1
-
alleles:
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alleles:
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73424772
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424784
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424791
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424796
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424807
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73424808
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424810
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424811
strand: 1
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alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs2145593063
seq_region_name: 17
source: dbSNP
start: 73424816
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063266315
seq_region_name: 17
source: dbSNP
start: 73424818
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs983764646
seq_region_name: 17
source: dbSNP
start: 73424819
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424819
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599554044
seq_region_name: 17
source: dbSNP
start: 73424820
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145593105
seq_region_name: 17
source: dbSNP
start: 73424823
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424825
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063266448
seq_region_name: 17
source: dbSNP
start: 73424826
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424831
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1411522581
seq_region_name: 17
source: dbSNP
start: 73424833
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063266569
seq_region_name: 17
source: dbSNP
start: 73424835
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1312344431
seq_region_name: 17
source: dbSNP
start: 73424836
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1264769476
seq_region_name: 17
source: dbSNP
start: 73424845
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1847164483
seq_region_name: 17
source: dbSNP
start: 73424847
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1016624444
seq_region_name: 17
source: dbSNP
start: 73424851
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs925531224
seq_region_name: 17
source: dbSNP
start: 73424854
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424858
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs762782891
seq_region_name: 17
source: dbSNP
start: 73424858
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424860
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145593200
seq_region_name: 17
source: dbSNP
start: 73424863
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424864
feature_type: variation
id: rs1599554082
seq_region_name: 17
source: dbSNP
start: 73424864
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424865
feature_type: variation
id: rs2063266828
seq_region_name: 17
source: dbSNP
start: 73424865
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424867
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424867
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424868
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424868
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424871
feature_type: variation
id: rs2063266891
seq_region_name: 17
source: dbSNP
start: 73424871
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73424872
feature_type: variation
id: rs56774188
seq_region_name: 17
source: dbSNP
start: 73424872
strand: 1
-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- C
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- T
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
- G
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73424992
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73424994
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425002
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425003
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73425010
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425014
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425018
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425019
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs993662846
seq_region_name: 17
source: dbSNP
start: 73425021
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1481337193
seq_region_name: 17
source: dbSNP
start: 73425022
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425024
feature_type: variation
id: rs1193633173
seq_region_name: 17
source: dbSNP
start: 73425024
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425025
feature_type: variation
id: rs1407509077
seq_region_name: 17
source: dbSNP
start: 73425025
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249205863
seq_region_name: 17
source: dbSNP
start: 73425026
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425028
feature_type: variation
id: rs776841032
seq_region_name: 17
source: dbSNP
start: 73425028
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425030
feature_type: variation
id: rs1165638287
seq_region_name: 17
source: dbSNP
start: 73425030
strand: 1
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alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425034
feature_type: variation
id: rs1724179778
seq_region_name: 17
source: dbSNP
start: 73425034
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425035
feature_type: variation
id: rs555301394
seq_region_name: 17
source: dbSNP
start: 73425035
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425036
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73425037
feature_type: variation
id: rs139177223
seq_region_name: 17
source: dbSNP
start: 73425037
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425040
feature_type: variation
id: rs1452368972
seq_region_name: 17
source: dbSNP
start: 73425040
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1021466630
seq_region_name: 17
source: dbSNP
start: 73425044
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425046
feature_type: variation
id: rs2063268946
seq_region_name: 17
source: dbSNP
start: 73425046
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425048
feature_type: variation
id: rs533827495
seq_region_name: 17
source: dbSNP
start: 73425048
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425049
feature_type: variation
id: rs1006488028
seq_region_name: 17
source: dbSNP
start: 73425049
strand: 1
-
alleles:
- TCTACTAAAAATACAGAAATTTGCCGGGCGTGGTGGCCAGTG
- TCTACTAAAAATACAGAAATTTGCCGGGCGTGGTGGCCAGTGTCTACTAAAAATACAGAAATTTGCCGGGCGTGGTGGCCAGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425093
feature_type: variation
id: rs2063268999
seq_region_name: 17
source: dbSNP
start: 73425052
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063269029
seq_region_name: 17
source: dbSNP
start: 73425055
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425056
feature_type: variation
id: rs1271047819
seq_region_name: 17
source: dbSNP
start: 73425056
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425057
feature_type: variation
id: rs1479636757
seq_region_name: 17
source: dbSNP
start: 73425057
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425059
feature_type: variation
id: rs549019260
seq_region_name: 17
source: dbSNP
start: 73425059
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425063
feature_type: variation
id: rs2063269130
seq_region_name: 17
source: dbSNP
start: 73425063
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425064
feature_type: variation
id: rs2063269169
seq_region_name: 17
source: dbSNP
start: 73425064
strand: 1
-
alleles:
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- "-"
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425192
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425193
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425195
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425196
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425197
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425198
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73425199
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425201
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73425203
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425204
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425206
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs577896361
seq_region_name: 17
source: dbSNP
start: 73425209
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425212
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425215
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425216
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063271115
seq_region_name: 17
source: dbSNP
start: 73425217
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425218
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73425220
strand: 1
-
alleles:
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- AAAA
- AAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425220
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425224
feature_type: variation
id: rs919001207
seq_region_name: 17
source: dbSNP
start: 73425224
strand: 1
-
alleles:
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- ACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425224
strand: 1
-
alleles:
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- AAAA
- AAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425230
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425231
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425235
feature_type: variation
id: rs2063271313
seq_region_name: 17
source: dbSNP
start: 73425235
strand: 1
-
alleles:
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- CCCCCC
- CCCCCCCC
- CCCCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425242
feature_type: variation
id: rs910456937
seq_region_name: 17
source: dbSNP
start: 73425236
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425237
feature_type: variation
id: rs950545369
seq_region_name: 17
source: dbSNP
start: 73425237
strand: 1
-
alleles:
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425273
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425275
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425277
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425281
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425282
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425298
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425299
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73425301
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425305
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425306
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425307
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425309
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425313
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425321
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425323
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs949242512
seq_region_name: 17
source: dbSNP
start: 73425324
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425326
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425327
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425329
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425330
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425332
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73425340
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425342
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145594629
seq_region_name: 17
source: dbSNP
start: 73425343
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425346
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1368189898
seq_region_name: 17
source: dbSNP
start: 73425349
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1001326891
seq_region_name: 17
source: dbSNP
start: 73425352
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs367649415
seq_region_name: 17
source: dbSNP
start: 73425353
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73425357
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1169467577
seq_region_name: 17
source: dbSNP
start: 73425359
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425362
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425364
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425367
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs147688000
seq_region_name: 17
source: dbSNP
start: 73425368
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425370
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425374
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063272982
seq_region_name: 17
source: dbSNP
start: 73425375
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063273018
seq_region_name: 17
source: dbSNP
start: 73425375
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063273063
seq_region_name: 17
source: dbSNP
start: 73425376
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425379
feature_type: variation
id: rs1019816828
seq_region_name: 17
source: dbSNP
start: 73425379
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1193375225
seq_region_name: 17
source: dbSNP
start: 73425386
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425389
feature_type: variation
id: rs1434290235
seq_region_name: 17
source: dbSNP
start: 73425389
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063273179
seq_region_name: 17
source: dbSNP
start: 73425393
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs957147532
seq_region_name: 17
source: dbSNP
start: 73425397
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1428301193
seq_region_name: 17
source: dbSNP
start: 73425398
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1288226938
seq_region_name: 17
source: dbSNP
start: 73425399
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1273200058
seq_region_name: 17
source: dbSNP
start: 73425400
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs966043007
seq_region_name: 17
source: dbSNP
start: 73425401
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1011335365
seq_region_name: 17
source: dbSNP
start: 73425402
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145594784
seq_region_name: 17
source: dbSNP
start: 73425402
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1797108525
seq_region_name: 17
source: dbSNP
start: 73425404
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425405
feature_type: variation
id: rs747678855
seq_region_name: 17
source: dbSNP
start: 73425405
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425406
feature_type: variation
id: rs1232222721
seq_region_name: 17
source: dbSNP
start: 73425406
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425408
feature_type: variation
id: rs1312517660
seq_region_name: 17
source: dbSNP
start: 73425408
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425409
feature_type: variation
id: rs2063273467
seq_region_name: 17
source: dbSNP
start: 73425409
strand: 1
-
alleles:
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- GCACTGCAGCACTGCAGCACTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425427
feature_type: variation
id: rs2063273486
seq_region_name: 17
source: dbSNP
start: 73425413
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425417
feature_type: variation
id: rs186315510
seq_region_name: 17
source: dbSNP
start: 73425417
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425418
feature_type: variation
id: rs2063273541
seq_region_name: 17
source: dbSNP
start: 73425418
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425419
feature_type: variation
id: rs976411218
seq_region_name: 17
source: dbSNP
start: 73425419
strand: 1
-
alleles:
- GCACTGCTGCA
- GCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425431
feature_type: variation
id: rs1350018829
seq_region_name: 17
source: dbSNP
start: 73425421
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425424
feature_type: variation
id: rs1454505057
seq_region_name: 17
source: dbSNP
start: 73425424
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425427
feature_type: variation
id: rs1411955977
seq_region_name: 17
source: dbSNP
start: 73425427
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425431
feature_type: variation
id: rs1026210457
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strand: 1
-
alleles:
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-
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alleles:
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-
alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425587
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425594
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425596
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425600
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425601
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425602
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425603
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063275033
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs934314813
seq_region_name: 17
source: dbSNP
start: 73425610
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063275085
seq_region_name: 17
source: dbSNP
start: 73425611
strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2063275110
seq_region_name: 17
source: dbSNP
start: 73425615
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1396753313
seq_region_name: 17
source: dbSNP
start: 73425616
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1404887086
seq_region_name: 17
source: dbSNP
start: 73425617
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1006827300
seq_region_name: 17
source: dbSNP
start: 73425618
strand: 1
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alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425621
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063275263
seq_region_name: 17
source: dbSNP
start: 73425622
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1041052456
seq_region_name: 17
source: dbSNP
start: 73425628
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425632
feature_type: variation
id: rs1413305190
seq_region_name: 17
source: dbSNP
start: 73425632
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425633
feature_type: variation
id: rs566708568
seq_region_name: 17
source: dbSNP
start: 73425633
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425637
feature_type: variation
id: rs2063275362
seq_region_name: 17
source: dbSNP
start: 73425637
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425640
feature_type: variation
id: rs2063275402
seq_region_name: 17
source: dbSNP
start: 73425640
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063275418
seq_region_name: 17
source: dbSNP
start: 73425646
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs534056872
seq_region_name: 17
source: dbSNP
start: 73425648
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425650
feature_type: variation
id: rs2063275468
seq_region_name: 17
source: dbSNP
start: 73425650
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425652
feature_type: variation
id: rs147959734
seq_region_name: 17
source: dbSNP
start: 73425652
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1025897065
seq_region_name: 17
source: dbSNP
start: 73425653
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425654
feature_type: variation
id: rs1186413428
seq_region_name: 17
source: dbSNP
start: 73425654
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425655
feature_type: variation
id: rs1442625013
seq_region_name: 17
source: dbSNP
start: 73425655
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1258065023
seq_region_name: 17
source: dbSNP
start: 73425656
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063275592
seq_region_name: 17
source: dbSNP
start: 73425658
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063275615
seq_region_name: 17
source: dbSNP
start: 73425661
strand: 1
-
alleles:
- ACGCCCGAC
- AC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425671
feature_type: variation
id: rs1206551613
seq_region_name: 17
source: dbSNP
start: 73425663
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425664
feature_type: variation
id: rs573740842
seq_region_name: 17
source: dbSNP
start: 73425664
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425665
feature_type: variation
id: rs1268716643
seq_region_name: 17
source: dbSNP
start: 73425665
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425666
feature_type: variation
id: rs1005756256
seq_region_name: 17
source: dbSNP
start: 73425666
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73425667
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73425829
strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73425845
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73425876
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425883
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425884
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425886
strand: 1
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-
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- ATTTGTTACAGTAA
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73425980
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73425985
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425987
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425989
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425992
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73425993
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73425995
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426001
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426002
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426005
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426006
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063278778
seq_region_name: 17
source: dbSNP
start: 73426008
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426013
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs989369388
seq_region_name: 17
source: dbSNP
start: 73426015
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1346543496
seq_region_name: 17
source: dbSNP
start: 73426016
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1198513245
seq_region_name: 17
source: dbSNP
start: 73426023
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063278897
seq_region_name: 17
source: dbSNP
start: 73426025
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063278924
seq_region_name: 17
source: dbSNP
start: 73426028
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063278949
seq_region_name: 17
source: dbSNP
start: 73426033
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1358418640
seq_region_name: 17
source: dbSNP
start: 73426036
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs183978445
seq_region_name: 17
source: dbSNP
start: 73426037
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063279037
seq_region_name: 17
source: dbSNP
start: 73426041
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426042
feature_type: variation
id: rs1472963329
seq_region_name: 17
source: dbSNP
start: 73426042
strand: 1
-
alleles:
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- TATTTTATTTT
- TATTTTATTTTATTTT
- TATTTTATTTTATTTTATTTTATTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426062
feature_type: variation
id: rs762591136
seq_region_name: 17
source: dbSNP
start: 73426042
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs187695988
seq_region_name: 17
source: dbSNP
start: 73426043
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063279108
seq_region_name: 17
source: dbSNP
start: 73426044
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs534118912
seq_region_name: 17
source: dbSNP
start: 73426046
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426047
feature_type: variation
id: rs1345002447
seq_region_name: 17
source: dbSNP
start: 73426047
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063279173
seq_region_name: 17
source: dbSNP
start: 73426049
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426050
feature_type: variation
id: rs1238453921
seq_region_name: 17
source: dbSNP
start: 73426050
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426054
feature_type: variation
id: rs1212656849
seq_region_name: 17
source: dbSNP
start: 73426054
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426061
feature_type: variation
id: rs2063279239
seq_region_name: 17
source: dbSNP
start: 73426061
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063279264
seq_region_name: 17
source: dbSNP
start: 73426065
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426069
feature_type: variation
id: rs765952245
seq_region_name: 17
source: dbSNP
start: 73426069
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426070
feature_type: variation
id: rs555502005
seq_region_name: 17
source: dbSNP
start: 73426070
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426071
feature_type: variation
id: rs1329248172
seq_region_name: 17
source: dbSNP
start: 73426071
strand: 1
-
alleles:
- ATCTCA
- ATCTCATCTCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426076
feature_type: variation
id: rs1268084915
seq_region_name: 17
source: dbSNP
start: 73426071
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426072
feature_type: variation
id: rs2063279380
seq_region_name: 17
source: dbSNP
start: 73426072
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426073
feature_type: variation
id: rs368085023
seq_region_name: 17
source: dbSNP
start: 73426073
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426075
feature_type: variation
id: rs1377944751
seq_region_name: 17
source: dbSNP
start: 73426075
strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426080
feature_type: variation
id: rs1275260444
seq_region_name: 17
source: dbSNP
start: 73426077
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426079
feature_type: variation
id: rs922742969
seq_region_name: 17
source: dbSNP
start: 73426079
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426082
feature_type: variation
id: rs564155943
seq_region_name: 17
source: dbSNP
start: 73426080
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426083
feature_type: variation
id: rs1599555246
seq_region_name: 17
source: dbSNP
start: 73426083
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426087
feature_type: variation
id: rs2063279552
seq_region_name: 17
source: dbSNP
start: 73426087
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426091
feature_type: variation
id: rs2063279579
seq_region_name: 17
source: dbSNP
start: 73426091
strand: 1
-
alleles:
- CTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGATTACAGGCCTG
- CTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426192
feature_type: variation
id: rs2063279612
seq_region_name: 17
source: dbSNP
start: 73426091
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063279649
seq_region_name: 17
source: dbSNP
start: 73426092
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs929962917
seq_region_name: 17
source: dbSNP
start: 73426094
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1457693971
seq_region_name: 17
source: dbSNP
start: 73426098
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426106
feature_type: variation
id: rs2063279760
seq_region_name: 17
source: dbSNP
start: 73426106
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs192369668
seq_region_name: 17
source: dbSNP
start: 73426107
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426108
feature_type: variation
id: rs888685840
seq_region_name: 17
source: dbSNP
start: 73426108
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426110
feature_type: variation
id: rs941572764
seq_region_name: 17
source: dbSNP
start: 73426110
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426115
feature_type: variation
id: rs1405041128
seq_region_name: 17
source: dbSNP
start: 73426115
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426116
feature_type: variation
id: rs1056062952
seq_region_name: 17
source: dbSNP
start: 73426116
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426118
feature_type: variation
id: rs2145596527
seq_region_name: 17
source: dbSNP
start: 73426118
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426123
feature_type: variation
id: rs2063279926
seq_region_name: 17
source: dbSNP
start: 73426123
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426125
feature_type: variation
id: rs1599555274
seq_region_name: 17
source: dbSNP
start: 73426125
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426127
feature_type: variation
id: rs2063279978
seq_region_name: 17
source: dbSNP
start: 73426127
strand: 1
-
alleles:
- CCGCCTCCCG
- CCGCCTCCCGCCTCCCG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426138
feature_type: variation
id: rs2063279997
seq_region_name: 17
source: dbSNP
start: 73426129
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426130
feature_type: variation
id: rs1197098739
seq_region_name: 17
source: dbSNP
start: 73426130
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426131
feature_type: variation
id: rs1183776001
seq_region_name: 17
source: dbSNP
start: 73426131
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426132
feature_type: variation
id: rs2145596556
seq_region_name: 17
source: dbSNP
start: 73426132
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426137
feature_type: variation
id: rs560688817
seq_region_name: 17
source: dbSNP
start: 73426137
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426138
feature_type: variation
id: rs894615944
seq_region_name: 17
source: dbSNP
start: 73426138
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426140
feature_type: variation
id: rs2063280124
seq_region_name: 17
source: dbSNP
start: 73426140
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426148
feature_type: variation
id: rs2145596587
seq_region_name: 17
source: dbSNP
start: 73426148
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426149
feature_type: variation
id: rs759206266
seq_region_name: 17
source: dbSNP
start: 73426149
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426150
feature_type: variation
id: rs2063280178
seq_region_name: 17
source: dbSNP
start: 73426150
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426152
feature_type: variation
id: rs9674480
seq_region_name: 17
source: dbSNP
start: 73426152
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426154
feature_type: variation
id: rs2063280224
seq_region_name: 17
source: dbSNP
start: 73426154
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426155
feature_type: variation
id: rs1475729783
seq_region_name: 17
source: dbSNP
start: 73426155
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426156
feature_type: variation
id: rs2063280275
seq_region_name: 17
source: dbSNP
start: 73426156
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426158
feature_type: variation
id: rs2063280297
seq_region_name: 17
source: dbSNP
start: 73426158
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426163
feature_type: variation
id: rs1218710256
seq_region_name: 17
source: dbSNP
start: 73426163
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426166
feature_type: variation
id: rs1169528503
seq_region_name: 17
source: dbSNP
start: 73426166
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426170
feature_type: variation
id: rs2063280363
seq_region_name: 17
source: dbSNP
start: 73426170
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426173
feature_type: variation
id: rs1568398904
seq_region_name: 17
source: dbSNP
start: 73426173
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426174
feature_type: variation
id: rs2063280402
seq_region_name: 17
source: dbSNP
start: 73426174
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426175
feature_type: variation
id: rs1416808108
seq_region_name: 17
source: dbSNP
start: 73426175
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426181
feature_type: variation
id: rs2063280426
seq_region_name: 17
source: dbSNP
start: 73426181
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426182
feature_type: variation
id: rs1290161559
seq_region_name: 17
source: dbSNP
start: 73426182
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426183
feature_type: variation
id: rs1247646180
seq_region_name: 17
source: dbSNP
start: 73426183
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426185
feature_type: variation
id: rs971180302
seq_region_name: 17
source: dbSNP
start: 73426185
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426188
feature_type: variation
id: rs2145596682
seq_region_name: 17
source: dbSNP
start: 73426188
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426190
feature_type: variation
id: rs1428465805
seq_region_name: 17
source: dbSNP
start: 73426190
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426191
feature_type: variation
id: rs1163843531
seq_region_name: 17
source: dbSNP
start: 73426191
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426192
feature_type: variation
id: rs1003638925
seq_region_name: 17
source: dbSNP
start: 73426192
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426195
feature_type: variation
id: rs1402710464
seq_region_name: 17
source: dbSNP
start: 73426195
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426196
feature_type: variation
id: rs2063280618
seq_region_name: 17
source: dbSNP
start: 73426196
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426197
feature_type: variation
id: rs2063280635
seq_region_name: 17
source: dbSNP
start: 73426197
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426198
feature_type: variation
id: rs2063280656
seq_region_name: 17
source: dbSNP
start: 73426198
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426202
feature_type: variation
id: rs1031077752
seq_region_name: 17
source: dbSNP
start: 73426202
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426203
feature_type: variation
id: rs956866102
seq_region_name: 17
source: dbSNP
start: 73426203
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426204
feature_type: variation
id: rs1322027928
seq_region_name: 17
source: dbSNP
start: 73426204
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426206
feature_type: variation
id: rs1457496237
seq_region_name: 17
source: dbSNP
start: 73426206
strand: 1
-
alleles:
- "-"
- A
- T
- TT
- TTTT
- TTTTT
- TTTTTT
- TTTTTTTT
- TTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426207
feature_type: variation
id: rs1432134156
seq_region_name: 17
source: dbSNP
start: 73426208
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426208
feature_type: variation
id: rs1372982690
seq_region_name: 17
source: dbSNP
start: 73426208
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426208
feature_type: variation
id: rs2063280854
seq_region_name: 17
source: dbSNP
start: 73426208
strand: 1
-
alleles:
- CT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426209
feature_type: variation
id: rs2063280880
seq_region_name: 17
source: dbSNP
start: 73426208
strand: 1
-
alleles:
- "-"
- A
- G
- GT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426208
feature_type: variation
id: rs2063280905
seq_region_name: 17
source: dbSNP
start: 73426209
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426209
feature_type: variation
id: rs1434254297
seq_region_name: 17
source: dbSNP
start: 73426209
strand: 1
-
alleles:
- TTT
- TTTGTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426211
feature_type: variation
id: rs2063280945
seq_region_name: 17
source: dbSNP
start: 73426209
strand: 1
-
alleles:
- TTTT
- TTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426212
feature_type: variation
id: rs2063280960
seq_region_name: 17
source: dbSNP
start: 73426209
strand: 1
-
alleles:
- TTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426236
feature_type: variation
id: rs751417057
seq_region_name: 17
source: dbSNP
start: 73426209
strand: 1
-
alleles:
- TTTTTTTTTTTTTTT
- TTTTTTTTTTTTTTTGTTTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426227
feature_type: variation
id: rs2145596841
seq_region_name: 17
source: dbSNP
start: 73426213
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426219
feature_type: variation
id: rs2063281242
seq_region_name: 17
source: dbSNP
start: 73426220
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426220
feature_type: variation
id: rs2063281262
seq_region_name: 17
source: dbSNP
start: 73426220
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426224
feature_type: variation
id: rs2063281293
seq_region_name: 17
source: dbSNP
start: 73426224
strand: 1
-
alleles:
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426236
feature_type: variation
id: rs2063281319
seq_region_name: 17
source: dbSNP
start: 73426224
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426225
feature_type: variation
id: rs1220509533
seq_region_name: 17
source: dbSNP
start: 73426225
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426226
feature_type: variation
id: rs1599555396
seq_region_name: 17
source: dbSNP
start: 73426226
strand: 1
-
alleles:
- TTTTTTTTTTTCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426238
feature_type: variation
id: rs1568398972
seq_region_name: 17
source: dbSNP
start: 73426226
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426226
feature_type: variation
id: rs2063281418
seq_region_name: 17
source: dbSNP
start: 73426227
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426227
feature_type: variation
id: rs1266437607
seq_region_name: 17
source: dbSNP
start: 73426227
strand: 1
-
alleles:
- TTTTTTTTTT
- TTTTTTTTTTTTTTTTTTCTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426236
feature_type: variation
id: rs2145596897
seq_region_name: 17
source: dbSNP
start: 73426227
strand: 1
-
alleles:
- "-"
- CTTTC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426227
feature_type: variation
id: rs2063281461
seq_region_name: 17
source: dbSNP
start: 73426228
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426228
feature_type: variation
id: rs1599555407
seq_region_name: 17
source: dbSNP
start: 73426228
strand: 1
-
alleles:
- TTTTTTTTT
- TTTTTTTTTTGTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426236
feature_type: variation
id: rs2063281503
seq_region_name: 17
source: dbSNP
start: 73426228
strand: 1
-
alleles:
- TTTTTTTTTCT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426238
feature_type: variation
id: rs2063281537
seq_region_name: 17
source: dbSNP
start: 73426228
strand: 1
-
alleles:
- T
- TCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426229
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426232
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426234
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426234
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426235
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426235
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063282136
seq_region_name: 17
source: dbSNP
start: 73426236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426237
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426237
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426237
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs12945964
seq_region_name: 17
source: dbSNP
start: 73426238
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs369071570
seq_region_name: 17
source: dbSNP
start: 73426239
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1386522320
seq_region_name: 17
source: dbSNP
start: 73426239
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426240
strand: 1
-
alleles:
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- TTTTT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426240
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs372505071
seq_region_name: 17
source: dbSNP
start: 73426241
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426242
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426243
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426244
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1171863336
seq_region_name: 17
source: dbSNP
start: 73426245
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426246
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426247
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426247
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426247
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426248
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1555767589
seq_region_name: 17
source: dbSNP
start: 73426249
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1320684186
seq_region_name: 17
source: dbSNP
start: 73426250
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1401593232
seq_region_name: 17
source: dbSNP
start: 73426250
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063283090
seq_region_name: 17
source: dbSNP
start: 73426252
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1393351073
seq_region_name: 17
source: dbSNP
start: 73426253
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs372305277
seq_region_name: 17
source: dbSNP
start: 73426255
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1434972443
seq_region_name: 17
source: dbSNP
start: 73426256
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145597231
seq_region_name: 17
source: dbSNP
start: 73426258
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs974788234
seq_region_name: 17
source: dbSNP
start: 73426265
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145597245
seq_region_name: 17
source: dbSNP
start: 73426267
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs59953817
seq_region_name: 17
source: dbSNP
start: 73426269
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063283232
seq_region_name: 17
source: dbSNP
start: 73426272
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs933017464
seq_region_name: 17
source: dbSNP
start: 73426273
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063283270
seq_region_name: 17
source: dbSNP
start: 73426274
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599555521
seq_region_name: 17
source: dbSNP
start: 73426277
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs577940055
seq_region_name: 17
source: dbSNP
start: 73426278
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1051508147
seq_region_name: 17
source: dbSNP
start: 73426280
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063283364
seq_region_name: 17
source: dbSNP
start: 73426282
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063283387
seq_region_name: 17
source: dbSNP
start: 73426285
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs8067496
seq_region_name: 17
source: dbSNP
start: 73426286
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs554103337
seq_region_name: 17
source: dbSNP
start: 73426287
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599555544
seq_region_name: 17
source: dbSNP
start: 73426289
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063283568
seq_region_name: 17
source: dbSNP
start: 73426290
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145597344
seq_region_name: 17
source: dbSNP
start: 73426296
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1265013850
seq_region_name: 17
source: dbSNP
start: 73426297
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426298
feature_type: variation
id: rs1831480424
seq_region_name: 17
source: dbSNP
start: 73426298
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426300
feature_type: variation
id: rs1483424324
seq_region_name: 17
source: dbSNP
start: 73426300
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1264957804
seq_region_name: 17
source: dbSNP
start: 73426302
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426303
feature_type: variation
id: rs1328654426
seq_region_name: 17
source: dbSNP
start: 73426303
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426304
feature_type: variation
id: rs1599555560
seq_region_name: 17
source: dbSNP
start: 73426304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426308
feature_type: variation
id: rs1289065384
seq_region_name: 17
source: dbSNP
start: 73426308
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426309
feature_type: variation
id: rs957718805
seq_region_name: 17
source: dbSNP
start: 73426309
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426310
feature_type: variation
id: rs1439179508
seq_region_name: 17
source: dbSNP
start: 73426310
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426311
feature_type: variation
id: rs2063283919
seq_region_name: 17
source: dbSNP
start: 73426311
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426312
feature_type: variation
id: rs1312218910
seq_region_name: 17
source: dbSNP
start: 73426312
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426313
feature_type: variation
id: rs1037552815
seq_region_name: 17
source: dbSNP
start: 73426313
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426315
feature_type: variation
id: rs2063283998
seq_region_name: 17
source: dbSNP
start: 73426315
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426317
feature_type: variation
id: rs1206734174
seq_region_name: 17
source: dbSNP
start: 73426317
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426318
feature_type: variation
id: rs1385352186
seq_region_name: 17
source: dbSNP
start: 73426318
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426319
feature_type: variation
id: rs1319145496
seq_region_name: 17
source: dbSNP
start: 73426319
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426321
feature_type: variation
id: rs1281878828
seq_region_name: 17
source: dbSNP
start: 73426321
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426322
feature_type: variation
id: rs572309127
seq_region_name: 17
source: dbSNP
start: 73426322
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73426323
feature_type: variation
id: rs899054481
seq_region_name: 17
source: dbSNP
start: 73426323
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426582
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73426593
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73426818
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426829
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426836
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426839
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73426972
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73426978
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73426978
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73426982
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427000
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427001
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427002
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427008
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427009
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427010
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427011
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427012
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs971806482
seq_region_name: 17
source: dbSNP
start: 73427017
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063289191
seq_region_name: 17
source: dbSNP
start: 73427018
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427025
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73427026
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427027
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427039
feature_type: variation
id: rs2063289274
seq_region_name: 17
source: dbSNP
start: 73427028
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427029
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427033
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs576833900
seq_region_name: 17
source: dbSNP
start: 73427034
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427035
feature_type: variation
id: rs2063289393
seq_region_name: 17
source: dbSNP
start: 73427035
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs939287755
seq_region_name: 17
source: dbSNP
start: 73427040
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427041
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427044
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063289494
seq_region_name: 17
source: dbSNP
start: 73427048
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1052344687
seq_region_name: 17
source: dbSNP
start: 73427051
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427053
feature_type: variation
id: rs1386170922
seq_region_name: 17
source: dbSNP
start: 73427053
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063289572
seq_region_name: 17
source: dbSNP
start: 73427060
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145599002
seq_region_name: 17
source: dbSNP
start: 73427062
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs7215575
seq_region_name: 17
source: dbSNP
start: 73427063
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145599024
seq_region_name: 17
source: dbSNP
start: 73427067
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1308763670
seq_region_name: 17
source: dbSNP
start: 73427068
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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id: rs1171798136
seq_region_name: 17
source: dbSNP
start: 73427070
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs914978309
seq_region_name: 17
source: dbSNP
start: 73427071
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427072
feature_type: variation
id: rs946760317
seq_region_name: 17
source: dbSNP
start: 73427072
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427075
feature_type: variation
id: rs2063289802
seq_region_name: 17
source: dbSNP
start: 73427075
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427076
feature_type: variation
id: rs2063289824
seq_region_name: 17
source: dbSNP
start: 73427076
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427079
feature_type: variation
id: rs946437583
seq_region_name: 17
source: dbSNP
start: 73427079
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427109
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73427112
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427113
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427116
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290258
seq_region_name: 17
source: dbSNP
start: 73427121
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs899946715
seq_region_name: 17
source: dbSNP
start: 73427124
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063290314
seq_region_name: 17
source: dbSNP
start: 73427130
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290341
seq_region_name: 17
source: dbSNP
start: 73427134
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs899465933
seq_region_name: 17
source: dbSNP
start: 73427141
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290393
seq_region_name: 17
source: dbSNP
start: 73427148
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs528558316
seq_region_name: 17
source: dbSNP
start: 73427161
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1479834219
seq_region_name: 17
source: dbSNP
start: 73427168
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063290452
seq_region_name: 17
source: dbSNP
start: 73427170
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290476
seq_region_name: 17
source: dbSNP
start: 73427172
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1429365975
seq_region_name: 17
source: dbSNP
start: 73427173
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs778210961
seq_region_name: 17
source: dbSNP
start: 73427174
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1262970012
seq_region_name: 17
source: dbSNP
start: 73427178
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1201220007
seq_region_name: 17
source: dbSNP
start: 73427183
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290612
seq_region_name: 17
source: dbSNP
start: 73427189
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063290635
seq_region_name: 17
source: dbSNP
start: 73427190
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290654
seq_region_name: 17
source: dbSNP
start: 73427193
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs996996965
seq_region_name: 17
source: dbSNP
start: 73427197
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1249618101
seq_region_name: 17
source: dbSNP
start: 73427205
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063290726
seq_region_name: 17
source: dbSNP
start: 73427209
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427219
feature_type: variation
id: rs752079430
seq_region_name: 17
source: dbSNP
start: 73427219
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427220
feature_type: variation
id: rs2145599327
seq_region_name: 17
source: dbSNP
start: 73427220
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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end: 73427249
feature_type: variation
id: rs1481469636
seq_region_name: 17
source: dbSNP
start: 73427249
strand: 1
-
alleles:
- GG
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145599338
seq_region_name: 17
source: dbSNP
start: 73427249
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427252
feature_type: variation
id: rs6501638
seq_region_name: 17
source: dbSNP
start: 73427252
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1202886510
seq_region_name: 17
source: dbSNP
start: 73427259
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063290877
seq_region_name: 17
source: dbSNP
start: 73427262
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063290894
seq_region_name: 17
source: dbSNP
start: 73427268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427269
feature_type: variation
id: rs1324431209
seq_region_name: 17
source: dbSNP
start: 73427269
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427270
feature_type: variation
id: rs1265072533
seq_region_name: 17
source: dbSNP
start: 73427270
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427273
feature_type: variation
id: rs2063290953
seq_region_name: 17
source: dbSNP
start: 73427273
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427274
feature_type: variation
id: rs2063290974
seq_region_name: 17
source: dbSNP
start: 73427274
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427280
feature_type: variation
id: rs2063291000
seq_region_name: 17
source: dbSNP
start: 73427280
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs887049938
seq_region_name: 17
source: dbSNP
start: 73427283
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427285
feature_type: variation
id: rs1004036240
seq_region_name: 17
source: dbSNP
start: 73427285
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs527997619
seq_region_name: 17
source: dbSNP
start: 73427292
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427293
feature_type: variation
id: rs1016748835
seq_region_name: 17
source: dbSNP
start: 73427293
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427294
feature_type: variation
id: rs549252888
seq_region_name: 17
source: dbSNP
start: 73427294
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427296
feature_type: variation
id: rs1425562974
seq_region_name: 17
source: dbSNP
start: 73427296
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427297
feature_type: variation
id: rs2063291170
seq_region_name: 17
source: dbSNP
start: 73427297
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427301
feature_type: variation
id: rs2063291188
seq_region_name: 17
source: dbSNP
start: 73427301
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427302
feature_type: variation
id: rs2063291209
seq_region_name: 17
source: dbSNP
start: 73427302
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427303
feature_type: variation
id: rs1015887339
seq_region_name: 17
source: dbSNP
start: 73427303
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427314
feature_type: variation
id: rs2063291262
seq_region_name: 17
source: dbSNP
start: 73427314
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427317
feature_type: variation
id: rs1470587368
seq_region_name: 17
source: dbSNP
start: 73427317
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427320
feature_type: variation
id: rs2145599471
seq_region_name: 17
source: dbSNP
start: 73427320
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427330
feature_type: variation
id: rs2063291304
seq_region_name: 17
source: dbSNP
start: 73427330
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427332
feature_type: variation
id: rs2063291338
seq_region_name: 17
source: dbSNP
start: 73427330
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427333
feature_type: variation
id: rs961703164
seq_region_name: 17
source: dbSNP
start: 73427333
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427335
feature_type: variation
id: rs1177942684
seq_region_name: 17
source: dbSNP
start: 73427335
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427336
feature_type: variation
id: rs1165663741
seq_region_name: 17
source: dbSNP
start: 73427336
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427340
feature_type: variation
id: rs1012966450
seq_region_name: 17
source: dbSNP
start: 73427340
strand: 1
-
alleles:
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- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427342
feature_type: variation
id: rs2063291453
seq_region_name: 17
source: dbSNP
start: 73427342
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427343
feature_type: variation
id: rs994528007
seq_region_name: 17
source: dbSNP
start: 73427343
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427345
feature_type: variation
id: rs1457169599
seq_region_name: 17
source: dbSNP
start: 73427345
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427346
feature_type: variation
id: rs1420666866
seq_region_name: 17
source: dbSNP
start: 73427346
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427348
feature_type: variation
id: rs2063291547
seq_region_name: 17
source: dbSNP
start: 73427348
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427353
feature_type: variation
id: rs1023479016
seq_region_name: 17
source: dbSNP
start: 73427353
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427360
feature_type: variation
id: rs969555692
seq_region_name: 17
source: dbSNP
start: 73427360
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427364
feature_type: variation
id: rs1461685184
seq_region_name: 17
source: dbSNP
start: 73427364
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427365
feature_type: variation
id: rs2145599559
seq_region_name: 17
source: dbSNP
start: 73427365
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427368
feature_type: variation
id: rs2063291630
seq_region_name: 17
source: dbSNP
start: 73427368
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427382
feature_type: variation
id: rs980605365
seq_region_name: 17
source: dbSNP
start: 73427382
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427390
feature_type: variation
id: rs8072989
seq_region_name: 17
source: dbSNP
start: 73427390
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427391
feature_type: variation
id: rs1382822924
seq_region_name: 17
source: dbSNP
start: 73427391
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427398
feature_type: variation
id: rs1349966468
seq_region_name: 17
source: dbSNP
start: 73427398
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427402
feature_type: variation
id: rs2063291767
seq_region_name: 17
source: dbSNP
start: 73427402
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427403
feature_type: variation
id: rs1241441987
seq_region_name: 17
source: dbSNP
start: 73427403
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427406
feature_type: variation
id: rs960576196
seq_region_name: 17
source: dbSNP
start: 73427406
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427408
feature_type: variation
id: rs2063291847
seq_region_name: 17
source: dbSNP
start: 73427408
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427409
feature_type: variation
id: rs1314759747
seq_region_name: 17
source: dbSNP
start: 73427409
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427412
feature_type: variation
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427510
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427511
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427512
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73427514
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427517
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs990372032
seq_region_name: 17
source: dbSNP
start: 73427524
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427525
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73427536
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427537
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427540
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427541
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427545
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427557
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427570
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427573
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427584
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427585
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427589
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427590
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427595
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427596
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427602
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427605
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1166160864
seq_region_name: 17
source: dbSNP
start: 73427606
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427607
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427615
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1445247090
seq_region_name: 17
source: dbSNP
start: 73427616
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1183834037
seq_region_name: 17
source: dbSNP
start: 73427617
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1475025585
seq_region_name: 17
source: dbSNP
start: 73427621
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427626
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1373769963
seq_region_name: 17
source: dbSNP
start: 73427627
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427628
feature_type: variation
id: rs1423455761
seq_region_name: 17
source: dbSNP
start: 73427628
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427635
feature_type: variation
id: rs2063293433
seq_region_name: 17
source: dbSNP
start: 73427635
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427638
feature_type: variation
id: rs2063293460
seq_region_name: 17
source: dbSNP
start: 73427638
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427640
feature_type: variation
id: rs1329711999
seq_region_name: 17
source: dbSNP
start: 73427640
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1354338627
seq_region_name: 17
source: dbSNP
start: 73427641
strand: 1
-
alleles:
- GC
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063293533
seq_region_name: 17
source: dbSNP
start: 73427641
strand: 1
-
alleles:
- "-"
- A
- AAA
- AAAA
- AAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427641
feature_type: variation
id: rs2063293549
seq_region_name: 17
source: dbSNP
start: 73427642
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427642
feature_type: variation
id: rs376864409
seq_region_name: 17
source: dbSNP
start: 73427642
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427642
feature_type: variation
id: rs1268449679
seq_region_name: 17
source: dbSNP
start: 73427642
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427643
feature_type: variation
id: rs1491335946
seq_region_name: 17
source: dbSNP
start: 73427642
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs775894423
seq_region_name: 17
source: dbSNP
start: 73427642
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427645
feature_type: variation
id: rs2063293689
seq_region_name: 17
source: dbSNP
start: 73427642
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427643
feature_type: variation
id: rs1346718704
seq_region_name: 17
source: dbSNP
start: 73427643
strand: 1
-
alleles:
- AAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAA
- AAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAGTCTTTTAAAAAAACAGGGCTGAAAAACCTTGACATCCACAAGAAAAAAAAAAAAAAAAAAAAAAAAAA
- AAAAAAAAAAAAAAAAAAAAAAAAAGAAGTCTTTTAAACAAACAGTGCTGAAAACCCTTGACATCCAAATGAAAAAAAAAAAAAAAAAAAAAAAAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427662
feature_type: variation
id: rs9302965
seq_region_name: 17
source: dbSNP
start: 73427643
strand: 1
-
alleles:
- AA
- AACAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73427646
feature_type: variation
id: rs2063293941
seq_region_name: 17
source: dbSNP
start: 73427645
strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73427791
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73427795
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427805
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427809
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427810
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427812
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427814
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427819
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73427823
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73427824
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427825
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427829
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427830
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427834
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427844
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427846
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1358024908
seq_region_name: 17
source: dbSNP
start: 73427852
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427853
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427865
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427866
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427871
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427872
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73427877
strand: 1
-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428029
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73428031
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73428033
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428037
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428040
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428047
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428051
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428054
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73428059
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73428063
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428066
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428070
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs974907483
seq_region_name: 17
source: dbSNP
start: 73428074
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428075
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73428076
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428088
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063297107
seq_region_name: 17
source: dbSNP
start: 73428089
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428092
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428094
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs955271887
seq_region_name: 17
source: dbSNP
start: 73428095
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145601074
seq_region_name: 17
source: dbSNP
start: 73428096
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428101
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428102
feature_type: variation
id: rs773835965
seq_region_name: 17
source: dbSNP
start: 73428102
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428104
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428105
feature_type: variation
id: rs1431515498
seq_region_name: 17
source: dbSNP
start: 73428105
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063297286
seq_region_name: 17
source: dbSNP
start: 73428108
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428110
feature_type: variation
id: rs1362729003
seq_region_name: 17
source: dbSNP
start: 73428110
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1301457142
seq_region_name: 17
source: dbSNP
start: 73428113
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428114
feature_type: variation
id: rs1051612874
seq_region_name: 17
source: dbSNP
start: 73428114
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1366566558
seq_region_name: 17
source: dbSNP
start: 73428118
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1166088234
seq_region_name: 17
source: dbSNP
start: 73428125
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063297419
seq_region_name: 17
source: dbSNP
start: 73428126
strand: 1
-
alleles:
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- AACAAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428136
feature_type: variation
id: rs1427224236
seq_region_name: 17
source: dbSNP
start: 73428128
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428129
feature_type: variation
id: rs771058199
seq_region_name: 17
source: dbSNP
start: 73428129
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428132
feature_type: variation
id: rs1416828076
seq_region_name: 17
source: dbSNP
start: 73428132
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428133
feature_type: variation
id: rs1185453546
seq_region_name: 17
source: dbSNP
start: 73428133
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428136
feature_type: variation
id: rs908164597
seq_region_name: 17
source: dbSNP
start: 73428136
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428138
feature_type: variation
id: rs2063297564
seq_region_name: 17
source: dbSNP
start: 73428138
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428141
feature_type: variation
id: rs912673085
seq_region_name: 17
source: dbSNP
start: 73428141
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs749550367
seq_region_name: 17
source: dbSNP
start: 73428144
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73428148
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1490144868
seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1038285493
seq_region_name: 17
source: dbSNP
start: 73428152
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428157
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1223742136
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063297758
seq_region_name: 17
source: dbSNP
start: 73428167
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1305718354
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
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feature_type: variation
id: rs2145601246
seq_region_name: 17
source: dbSNP
start: 73428169
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs143806432
seq_region_name: 17
source: dbSNP
start: 73428173
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2145601258
seq_region_name: 17
source: dbSNP
start: 73428175
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063297827
seq_region_name: 17
source: dbSNP
start: 73428178
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1272160709
seq_region_name: 17
source: dbSNP
start: 73428182
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2345419
seq_region_name: 17
source: dbSNP
start: 73428183
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063297901
seq_region_name: 17
source: dbSNP
start: 73428183
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063297915
seq_region_name: 17
source: dbSNP
start: 73428185
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs948516375
seq_region_name: 17
source: dbSNP
start: 73428187
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs764876493
seq_region_name: 17
source: dbSNP
start: 73428194
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599556962
seq_region_name: 17
source: dbSNP
start: 73428195
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063298029
seq_region_name: 17
source: dbSNP
start: 73428197
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063298056
seq_region_name: 17
source: dbSNP
start: 73428199
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs147276739
seq_region_name: 17
source: dbSNP
start: 73428202
strand: 1
-
alleles:
- "-"
- G
- GTGGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1346580205
seq_region_name: 17
source: dbSNP
start: 73428203
strand: 1
-
alleles:
- T
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- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063298141
seq_region_name: 17
source: dbSNP
start: 73428203
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1340352864
seq_region_name: 17
source: dbSNP
start: 73428204
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1003344003
seq_region_name: 17
source: dbSNP
start: 73428204
strand: 1
-
alleles:
- CCTAGC
- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1460739430
seq_region_name: 17
source: dbSNP
start: 73428204
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428206
strand: 1
-
alleles:
- AG
- "-"
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1292268854
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- A
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428210
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428211
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1048688682
seq_region_name: 17
source: dbSNP
start: 73428213
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428216
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063298410
seq_region_name: 17
source: dbSNP
start: 73428217
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428218
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1001902412
seq_region_name: 17
source: dbSNP
start: 73428219
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428220
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063298485
seq_region_name: 17
source: dbSNP
start: 73428221
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1196891637
seq_region_name: 17
source: dbSNP
start: 73428223
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428225
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1453047699
seq_region_name: 17
source: dbSNP
start: 73428226
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428227
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1053210106
seq_region_name: 17
source: dbSNP
start: 73428229
strand: 1
-
alleles:
- TTTTTTTT
- TTTTTTT
- TTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1269094664
seq_region_name: 17
source: dbSNP
start: 73428230
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428232
strand: 1
-
alleles:
- TTTTTGTATTTTT
- TTTTT
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063298777
seq_region_name: 17
source: dbSNP
start: 73428233
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428234
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428238
feature_type: variation
id: rs1034719909
seq_region_name: 17
source: dbSNP
start: 73428238
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs140775130
seq_region_name: 17
source: dbSNP
start: 73428241
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428242
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1009334572
seq_region_name: 17
source: dbSNP
start: 73428245
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428247
feature_type: variation
id: rs1320174114
seq_region_name: 17
source: dbSNP
start: 73428247
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1246117331
seq_region_name: 17
source: dbSNP
start: 73428253
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063299023
seq_region_name: 17
source: dbSNP
start: 73428254
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs574069767
seq_region_name: 17
source: dbSNP
start: 73428255
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428257
feature_type: variation
id: rs1223179785
seq_region_name: 17
source: dbSNP
start: 73428257
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428259
feature_type: variation
id: rs1599557047
seq_region_name: 17
source: dbSNP
start: 73428259
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1324560377
seq_region_name: 17
source: dbSNP
start: 73428260
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1303625093
seq_region_name: 17
source: dbSNP
start: 73428262
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs967957541
seq_region_name: 17
source: dbSNP
start: 73428266
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428267
feature_type: variation
id: rs184561651
seq_region_name: 17
source: dbSNP
start: 73428267
strand: 1
-
alleles:
- TGTTG
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063299286
seq_region_name: 17
source: dbSNP
start: 73428267
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063299320
seq_region_name: 17
source: dbSNP
start: 73428268
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428272
feature_type: variation
id: rs2063299351
seq_region_name: 17
source: dbSNP
start: 73428272
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428273
feature_type: variation
id: rs2145601588
seq_region_name: 17
source: dbSNP
start: 73428273
strand: 1
-
alleles:
- AGGA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428278
feature_type: variation
id: rs1189987978
seq_region_name: 17
source: dbSNP
start: 73428275
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428280
feature_type: variation
id: rs1387758542
seq_region_name: 17
source: dbSNP
start: 73428280
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428281
feature_type: variation
id: rs2063299473
seq_region_name: 17
source: dbSNP
start: 73428281
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428289
feature_type: variation
id: rs979751110
seq_region_name: 17
source: dbSNP
start: 73428289
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428294
feature_type: variation
id: rs2063299554
seq_region_name: 17
source: dbSNP
start: 73428294
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428300
feature_type: variation
id: rs545031440
seq_region_name: 17
source: dbSNP
start: 73428300
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428301
feature_type: variation
id: rs1021815340
seq_region_name: 17
source: dbSNP
start: 73428301
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428303
feature_type: variation
id: rs2063299610
seq_region_name: 17
source: dbSNP
start: 73428303
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428304
feature_type: variation
id: rs1599557083
seq_region_name: 17
source: dbSNP
start: 73428304
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428305
feature_type: variation
id: rs1391904188
seq_region_name: 17
source: dbSNP
start: 73428305
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428307
feature_type: variation
id: rs1039368732
seq_region_name: 17
source: dbSNP
start: 73428307
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428308
feature_type: variation
id: rs2063299748
seq_region_name: 17
source: dbSNP
start: 73428308
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428309
feature_type: variation
id: rs2063299779
seq_region_name: 17
source: dbSNP
start: 73428309
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428310
feature_type: variation
id: rs1401909560
seq_region_name: 17
source: dbSNP
start: 73428310
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428311
feature_type: variation
id: rs1407375252
seq_region_name: 17
source: dbSNP
start: 73428311
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428315
feature_type: variation
id: rs752321639
seq_region_name: 17
source: dbSNP
start: 73428315
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428316
feature_type: variation
id: rs542958484
seq_region_name: 17
source: dbSNP
start: 73428316
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428317
feature_type: variation
id: rs2063299981
seq_region_name: 17
source: dbSNP
start: 73428317
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428318
feature_type: variation
id: rs996455893
seq_region_name: 17
source: dbSNP
start: 73428318
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428324
feature_type: variation
id: rs1436420199
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs2063300078
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs2063300099
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063300116
seq_region_name: 17
source: dbSNP
start: 73428331
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599557116
seq_region_name: 17
source: dbSNP
start: 73428339
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1417146641
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- C
assembly_name: GRCh38
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feature_type: variation
id: rs1177748156
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063300238
seq_region_name: 17
source: dbSNP
start: 73428346
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568399868
seq_region_name: 17
source: dbSNP
start: 73428349
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs561411734
seq_region_name: 17
source: dbSNP
start: 73428352
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs78834970
seq_region_name: 17
source: dbSNP
start: 73428353
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1315928137
seq_region_name: 17
source: dbSNP
start: 73428355
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063300369
seq_region_name: 17
source: dbSNP
start: 73428356
strand: 1
-
alleles:
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- A
- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs908325623
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063300435
seq_region_name: 17
source: dbSNP
start: 73428363
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs372982442
seq_region_name: 17
source: dbSNP
start: 73428367
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063300460
seq_region_name: 17
source: dbSNP
start: 73428368
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063300488
seq_region_name: 17
source: dbSNP
start: 73428370
strand: 1
-
alleles:
- TTTTTTT
- TTTTTT
- TTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs912622120
seq_region_name: 17
source: dbSNP
start: 73428370
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063300553
seq_region_name: 17
source: dbSNP
start: 73428372
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs961028950
seq_region_name: 17
source: dbSNP
start: 73428374
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs972854418
seq_region_name: 17
source: dbSNP
start: 73428379
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs920097539
seq_region_name: 17
source: dbSNP
start: 73428380
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428383
feature_type: variation
id: rs1451302763
seq_region_name: 17
source: dbSNP
start: 73428383
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1447566118
seq_region_name: 17
source: dbSNP
start: 73428385
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1304299651
seq_region_name: 17
source: dbSNP
start: 73428388
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs973756261
seq_region_name: 17
source: dbSNP
start: 73428389
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs919828185
seq_region_name: 17
source: dbSNP
start: 73428390
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063300762
seq_region_name: 17
source: dbSNP
start: 73428393
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1363058944
seq_region_name: 17
source: dbSNP
start: 73428394
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1159045671
seq_region_name: 17
source: dbSNP
start: 73428401
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs527824029
seq_region_name: 17
source: dbSNP
start: 73428403
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428404
feature_type: variation
id: rs2145601920
seq_region_name: 17
source: dbSNP
start: 73428404
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145601925
seq_region_name: 17
source: dbSNP
start: 73428405
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428410
feature_type: variation
id: rs1383309576
seq_region_name: 17
source: dbSNP
start: 73428410
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1182850619
seq_region_name: 17
source: dbSNP
start: 73428414
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs543657274
seq_region_name: 17
source: dbSNP
start: 73428416
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1258342445
seq_region_name: 17
source: dbSNP
start: 73428418
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs764064060
seq_region_name: 17
source: dbSNP
start: 73428419
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428420
feature_type: variation
id: rs2063300932
seq_region_name: 17
source: dbSNP
start: 73428420
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428421
feature_type: variation
id: rs1261492979
seq_region_name: 17
source: dbSNP
start: 73428421
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428422
feature_type: variation
id: rs2063300971
seq_region_name: 17
source: dbSNP
start: 73428422
strand: 1
-
alleles:
- CAGGCCCTCACCCCTGCACCTG
- CAGGCCCTCACCCCTGCACCTGCTCAGGCCCTCACCCCTGCACCTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428443
feature_type: variation
id: rs1183833471
seq_region_name: 17
source: dbSNP
start: 73428422
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428426
feature_type: variation
id: rs1219253193
seq_region_name: 17
source: dbSNP
start: 73428426
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1357673422
seq_region_name: 17
source: dbSNP
start: 73428432
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428433
feature_type: variation
id: rs565448023
seq_region_name: 17
source: dbSNP
start: 73428433
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428437
feature_type: variation
id: rs906145654
seq_region_name: 17
source: dbSNP
start: 73428437
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428438
feature_type: variation
id: rs71380179
seq_region_name: 17
source: dbSNP
start: 73428438
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428440
feature_type: variation
id: rs1471603249
seq_region_name: 17
source: dbSNP
start: 73428440
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428442
feature_type: variation
id: rs1379974240
seq_region_name: 17
source: dbSNP
start: 73428442
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428443
feature_type: variation
id: rs1383824173
seq_region_name: 17
source: dbSNP
start: 73428443
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428444
feature_type: variation
id: rs1056077104
seq_region_name: 17
source: dbSNP
start: 73428444
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428448
feature_type: variation
id: rs2063301208
seq_region_name: 17
source: dbSNP
start: 73428448
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428450
feature_type: variation
id: rs547896976
seq_region_name: 17
source: dbSNP
start: 73428450
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428451
feature_type: variation
id: rs2063301287
seq_region_name: 17
source: dbSNP
start: 73428451
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428452
feature_type: variation
id: rs2063301310
seq_region_name: 17
source: dbSNP
start: 73428452
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428454
feature_type: variation
id: rs2063301325
seq_region_name: 17
source: dbSNP
start: 73428454
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428459
feature_type: variation
id: rs1390434730
seq_region_name: 17
source: dbSNP
start: 73428459
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428460
feature_type: variation
id: rs757371609
seq_region_name: 17
source: dbSNP
start: 73428460
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428461
feature_type: variation
id: rs2063301389
seq_region_name: 17
source: dbSNP
start: 73428461
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428465
feature_type: variation
id: rs1458259849
seq_region_name: 17
source: dbSNP
start: 73428465
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428467
feature_type: variation
id: rs2063301429
seq_region_name: 17
source: dbSNP
start: 73428467
strand: 1
-
alleles:
- GG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428471
feature_type: variation
id: rs2063301447
seq_region_name: 17
source: dbSNP
start: 73428470
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428471
feature_type: variation
id: rs2063301463
seq_region_name: 17
source: dbSNP
start: 73428471
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428472
feature_type: variation
id: rs2145602128
seq_region_name: 17
source: dbSNP
start: 73428472
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428474
feature_type: variation
id: rs566126153
seq_region_name: 17
source: dbSNP
start: 73428474
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428475
feature_type: variation
id: rs2063301515
seq_region_name: 17
source: dbSNP
start: 73428475
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428478
feature_type: variation
id: rs1473066827
seq_region_name: 17
source: dbSNP
start: 73428478
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428479
feature_type: variation
id: rs145839224
seq_region_name: 17
source: dbSNP
start: 73428479
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428480
feature_type: variation
id: rs2063301583
seq_region_name: 17
source: dbSNP
start: 73428480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428481
feature_type: variation
id: rs2063301596
seq_region_name: 17
source: dbSNP
start: 73428481
strand: 1
-
alleles:
- CACCAC
- CAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428486
feature_type: variation
id: rs1427927899
seq_region_name: 17
source: dbSNP
start: 73428481
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428486
feature_type: variation
id: rs2063301638
seq_region_name: 17
source: dbSNP
start: 73428486
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428488
feature_type: variation
id: rs1264191802
seq_region_name: 17
source: dbSNP
start: 73428488
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428492
feature_type: variation
id: rs1196105025
seq_region_name: 17
source: dbSNP
start: 73428492
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428494
feature_type: variation
id: rs2063301708
seq_region_name: 17
source: dbSNP
start: 73428494
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428500
feature_type: variation
id: rs2145602210
seq_region_name: 17
source: dbSNP
start: 73428500
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428504
feature_type: variation
id: rs2063301731
seq_region_name: 17
source: dbSNP
start: 73428504
strand: 1
-
alleles:
- GATCCTTTCTATTAGGTTGGTGC
- GATCCTTTCTATTAGGTTGGTGCGATCCTTTCTATTAGGTTGGTGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428531
feature_type: variation
id: rs2063301771
seq_region_name: 17
source: dbSNP
start: 73428509
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428511
feature_type: variation
id: rs891907842
seq_region_name: 17
source: dbSNP
start: 73428511
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428512
feature_type: variation
id: rs1386563308
seq_region_name: 17
source: dbSNP
start: 73428512
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428513
feature_type: variation
id: rs2063301835
seq_region_name: 17
source: dbSNP
start: 73428513
strand: 1
-
alleles:
- CTTTCT
- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428518
feature_type: variation
id: rs2063301855
seq_region_name: 17
source: dbSNP
start: 73428513
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428517
feature_type: variation
id: rs2063301879
seq_region_name: 17
source: dbSNP
start: 73428517
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- ACCGCAGTTACGTTTGCACCCACCACCGCAGTTACGTTTGCACCCACC
assembly_name: GRCh38
clinical_significance: []
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id: rs1242857720
seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
- CCACC
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73428622
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73428625
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428634
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428636
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428637
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428643
strand: 1
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alleles:
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- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428656
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428659
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428660
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428666
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428667
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428668
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428669
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428679
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428682
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428692
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063303190
seq_region_name: 17
source: dbSNP
start: 73428693
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs938497439
seq_region_name: 17
source: dbSNP
start: 73428700
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063303240
seq_region_name: 17
source: dbSNP
start: 73428705
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428713
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428718
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428719
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs769048644
seq_region_name: 17
source: dbSNP
start: 73428726
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1282174228
seq_region_name: 17
source: dbSNP
start: 73428728
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1436950554
seq_region_name: 17
source: dbSNP
start: 73428732
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428734
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428739
feature_type: variation
id: rs180846474
seq_region_name: 17
source: dbSNP
start: 73428739
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs927515523
seq_region_name: 17
source: dbSNP
start: 73428740
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428741
feature_type: variation
id: rs2063303449
seq_region_name: 17
source: dbSNP
start: 73428741
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428743
feature_type: variation
id: rs1401190283
seq_region_name: 17
source: dbSNP
start: 73428743
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428748
feature_type: variation
id: rs938951178
seq_region_name: 17
source: dbSNP
start: 73428748
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063303522
seq_region_name: 17
source: dbSNP
start: 73428749
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428751
feature_type: variation
id: rs2063303546
seq_region_name: 17
source: dbSNP
start: 73428751
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428752
feature_type: variation
id: rs2063303567
seq_region_name: 17
source: dbSNP
start: 73428752
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428753
feature_type: variation
id: rs2063303583
seq_region_name: 17
source: dbSNP
start: 73428753
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428754
feature_type: variation
id: rs2063303605
seq_region_name: 17
source: dbSNP
start: 73428754
strand: 1
-
alleles:
- TGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428757
feature_type: variation
id: rs773151992
seq_region_name: 17
source: dbSNP
start: 73428755
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428756
feature_type: variation
id: rs376125422
seq_region_name: 17
source: dbSNP
start: 73428756
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428758
feature_type: variation
id: rs1173318118
seq_region_name: 17
source: dbSNP
start: 73428758
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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start: 73428892
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428895
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428910
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428911
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73428912
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73428918
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428919
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73428920
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428921
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73428926
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73428928
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428929
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428932
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73428934
strand: 1
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alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428935
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73428939
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428941
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428945
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428946
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428950
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428951
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428961
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428962
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428963
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428964
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id: rs79412140
seq_region_name: 17
source: dbSNP
start: 73428964
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428965
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73428965
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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end: 73428967
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seq_region_name: 17
source: dbSNP
start: 73428967
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73428971
feature_type: variation
id: rs2063305503
seq_region_name: 17
source: dbSNP
start: 73428971
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1036615556
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429015
strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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feature_type: variation
id: rs755491754
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429033
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs77764850
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429037
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73429043
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429050
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429052
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429061
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429065
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429068
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063306217
seq_region_name: 17
source: dbSNP
start: 73429072
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429082
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429082
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429090
strand: 1
-
alleles:
- TAAGTAAGT
- TAAGT
assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429103
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429104
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1231977096
seq_region_name: 17
source: dbSNP
start: 73429105
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1599557743
seq_region_name: 17
source: dbSNP
start: 73429111
strand: 1
-
alleles:
- TTTTTT
- TTTTT
- TTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1477929841
seq_region_name: 17
source: dbSNP
start: 73429111
strand: 1
-
alleles:
- TT
- TTATAAAGATGACATT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs113509026
seq_region_name: 17
source: dbSNP
start: 73429112
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429114
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063306540
seq_region_name: 17
source: dbSNP
start: 73429117
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145603584
seq_region_name: 17
source: dbSNP
start: 73429118
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063306565
seq_region_name: 17
source: dbSNP
start: 73429120
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063306585
seq_region_name: 17
source: dbSNP
start: 73429121
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429122
feature_type: variation
id: rs2063306605
seq_region_name: 17
source: dbSNP
start: 73429122
strand: 1
-
alleles:
- AAAG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063306625
seq_region_name: 17
source: dbSNP
start: 73429123
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429126
feature_type: variation
id: rs1026992127
seq_region_name: 17
source: dbSNP
start: 73429126
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs905642586
seq_region_name: 17
source: dbSNP
start: 73429130
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063306689
seq_region_name: 17
source: dbSNP
start: 73429139
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1488002935
seq_region_name: 17
source: dbSNP
start: 73429140
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063306737
seq_region_name: 17
source: dbSNP
start: 73429142
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429147
feature_type: variation
id: rs2063306755
seq_region_name: 17
source: dbSNP
start: 73429147
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145603640
seq_region_name: 17
source: dbSNP
start: 73429161
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429163
feature_type: variation
id: rs1343925701
seq_region_name: 17
source: dbSNP
start: 73429163
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429165
feature_type: variation
id: rs1202531614
seq_region_name: 17
source: dbSNP
start: 73429165
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429169
feature_type: variation
id: rs1747736960
seq_region_name: 17
source: dbSNP
start: 73429169
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429171
feature_type: variation
id: rs952875384
seq_region_name: 17
source: dbSNP
start: 73429171
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429174
feature_type: variation
id: rs1305879670
seq_region_name: 17
source: dbSNP
start: 73429174
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063306856
seq_region_name: 17
source: dbSNP
start: 73429177
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145603675
seq_region_name: 17
source: dbSNP
start: 73429178
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429183
feature_type: variation
id: rs1257483654
seq_region_name: 17
source: dbSNP
start: 73429183
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429184
feature_type: variation
id: rs2063306896
seq_region_name: 17
source: dbSNP
start: 73429184
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429188
feature_type: variation
id: rs2063306921
seq_region_name: 17
source: dbSNP
start: 73429188
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429190
feature_type: variation
id: rs2063306937
seq_region_name: 17
source: dbSNP
start: 73429190
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429194
feature_type: variation
id: rs1001619425
seq_region_name: 17
source: dbSNP
start: 73429194
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429197
feature_type: variation
id: rs1599557784
seq_region_name: 17
source: dbSNP
start: 73429197
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429200
feature_type: variation
id: rs1320315865
seq_region_name: 17
source: dbSNP
start: 73429200
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429203
feature_type: variation
id: rs2063307021
seq_region_name: 17
source: dbSNP
start: 73429203
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429204
feature_type: variation
id: rs2063307042
seq_region_name: 17
source: dbSNP
start: 73429204
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429207
feature_type: variation
id: rs144569722
seq_region_name: 17
source: dbSNP
start: 73429207
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429208
feature_type: variation
id: rs548315412
seq_region_name: 17
source: dbSNP
start: 73429208
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429211
feature_type: variation
id: rs1368726672
seq_region_name: 17
source: dbSNP
start: 73429211
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429215
feature_type: variation
id: rs2063307129
seq_region_name: 17
source: dbSNP
start: 73429215
strand: 1
-
alleles:
- CAGCAG
- CAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429221
feature_type: variation
id: rs2063307155
seq_region_name: 17
source: dbSNP
start: 73429216
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429226
feature_type: variation
id: rs2063307176
seq_region_name: 17
source: dbSNP
start: 73429226
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429227
feature_type: variation
id: rs2063307203
seq_region_name: 17
source: dbSNP
start: 73429227
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429228
feature_type: variation
id: rs1192295858
seq_region_name: 17
source: dbSNP
start: 73429228
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429237
feature_type: variation
id: rs1295867894
seq_region_name: 17
source: dbSNP
start: 73429237
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429281
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429303
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429316
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429318
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429322
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429329
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429336
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429336
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429341
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1166901791
seq_region_name: 17
source: dbSNP
start: 73429348
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429353
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429354
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs874707
seq_region_name: 17
source: dbSNP
start: 73429355
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429356
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429359
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429367
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429371
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429373
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs773842881
seq_region_name: 17
source: dbSNP
start: 73429376
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063308401
seq_region_name: 17
source: dbSNP
start: 73429377
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429379
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429380
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429384
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs911856090
seq_region_name: 17
source: dbSNP
start: 73429386
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs940678338
seq_region_name: 17
source: dbSNP
start: 73429393
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1036607532
seq_region_name: 17
source: dbSNP
start: 73429402
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063308542
seq_region_name: 17
source: dbSNP
start: 73429404
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429405
feature_type: variation
id: rs2063308566
seq_region_name: 17
source: dbSNP
start: 73429405
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599557931
seq_region_name: 17
source: dbSNP
start: 73429407
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429411
feature_type: variation
id: rs2063308601
seq_region_name: 17
source: dbSNP
start: 73429411
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429415
feature_type: variation
id: rs2063308628
seq_region_name: 17
source: dbSNP
start: 73429415
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1257937964
seq_region_name: 17
source: dbSNP
start: 73429419
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429421
feature_type: variation
id: rs1214094747
seq_region_name: 17
source: dbSNP
start: 73429421
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429425
feature_type: variation
id: rs140313158
seq_region_name: 17
source: dbSNP
start: 73429425
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429428
feature_type: variation
id: rs1225729973
seq_region_name: 17
source: dbSNP
start: 73429428
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429435
feature_type: variation
id: rs2145604193
seq_region_name: 17
source: dbSNP
start: 73429435
strand: 1
-
alleles:
- CC
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429439
feature_type: variation
id: rs1599557949
seq_region_name: 17
source: dbSNP
start: 73429438
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429439
feature_type: variation
id: rs1599557952
seq_region_name: 17
source: dbSNP
start: 73429439
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429440
feature_type: variation
id: rs145336086
seq_region_name: 17
source: dbSNP
start: 73429440
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429442
feature_type: variation
id: rs2145604227
seq_region_name: 17
source: dbSNP
start: 73429442
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429444
feature_type: variation
id: rs888451978
seq_region_name: 17
source: dbSNP
start: 73429444
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429447
feature_type: variation
id: rs1001965487
seq_region_name: 17
source: dbSNP
start: 73429447
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429454
feature_type: variation
id: rs1321930485
seq_region_name: 17
source: dbSNP
start: 73429454
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429462
feature_type: variation
id: rs1309984912
seq_region_name: 17
source: dbSNP
start: 73429462
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429466
feature_type: variation
id: rs1034427535
seq_region_name: 17
source: dbSNP
start: 73429466
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429481
feature_type: variation
id: rs1045208274
seq_region_name: 17
source: dbSNP
start: 73429481
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429484
feature_type: variation
id: rs2063308875
seq_region_name: 17
source: dbSNP
start: 73429484
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429485
feature_type: variation
id: rs1222852173
seq_region_name: 17
source: dbSNP
start: 73429485
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429487
feature_type: variation
id: rs1394908620
seq_region_name: 17
source: dbSNP
start: 73429487
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429496
feature_type: variation
id: rs2063308941
seq_region_name: 17
source: dbSNP
start: 73429496
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429497
feature_type: variation
id: rs181253101
seq_region_name: 17
source: dbSNP
start: 73429497
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429498
feature_type: variation
id: rs1417690453
seq_region_name: 17
source: dbSNP
start: 73429498
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429508
feature_type: variation
id: rs1568400465
seq_region_name: 17
source: dbSNP
start: 73429505
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429508
feature_type: variation
id: rs1001254254
seq_region_name: 17
source: dbSNP
start: 73429508
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429509
feature_type: variation
id: rs1159217981
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73429599
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73429600
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73429601
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429603
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429604
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429606
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73429613
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063310184
seq_region_name: 17
source: dbSNP
start: 73429617
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1488542416
seq_region_name: 17
source: dbSNP
start: 73429618
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429619
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1320247728
seq_region_name: 17
source: dbSNP
start: 73429622
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429623
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1266671106
seq_region_name: 17
source: dbSNP
start: 73429624
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429625
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429626
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs537372097
seq_region_name: 17
source: dbSNP
start: 73429627
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429629
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1568400564
seq_region_name: 17
source: dbSNP
start: 73429630
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73429630
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429631
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429634
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1387257539
seq_region_name: 17
source: dbSNP
start: 73429635
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429638
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1568400576
seq_region_name: 17
source: dbSNP
start: 73429642
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs577573446
seq_region_name: 17
source: dbSNP
start: 73429645
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs541648569
seq_region_name: 17
source: dbSNP
start: 73429646
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs962034923
seq_region_name: 17
source: dbSNP
start: 73429647
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs888391706
seq_region_name: 17
source: dbSNP
start: 73429651
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs11650519
seq_region_name: 17
source: dbSNP
start: 73429654
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs575003788
seq_region_name: 17
source: dbSNP
start: 73429661
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs930860498
seq_region_name: 17
source: dbSNP
start: 73429664
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429666
feature_type: variation
id: rs1377390481
seq_region_name: 17
source: dbSNP
start: 73429666
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429668
feature_type: variation
id: rs1200253959
seq_region_name: 17
source: dbSNP
start: 73429668
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429671
feature_type: variation
id: rs1253829721
seq_region_name: 17
source: dbSNP
start: 73429671
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429672
feature_type: variation
id: rs2063310978
seq_region_name: 17
source: dbSNP
start: 73429672
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429676
feature_type: variation
id: rs2063311004
seq_region_name: 17
source: dbSNP
start: 73429676
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
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strand: 1
-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- CTCCTCCT
- CTCCT
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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consequence_type: intron_variant
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429807
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
- GGGGG
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429812
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs945701704
seq_region_name: 17
source: dbSNP
start: 73429813
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063311833
seq_region_name: 17
source: dbSNP
start: 73429816
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1013802048
seq_region_name: 17
source: dbSNP
start: 73429819
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429820
strand: 1
-
alleles:
- GG
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063311897
seq_region_name: 17
source: dbSNP
start: 73429825
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429826
strand: 1
-
alleles:
- "-"
- AAGCTAAAACCAGGAGGAGATTGTCCCTGCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429827
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1289344778
seq_region_name: 17
source: dbSNP
start: 73429828
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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seq_region_name: 17
source: dbSNP
start: 73429830
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429835
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429840
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429841
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429845
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73429846
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73429848
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs183904357
seq_region_name: 17
source: dbSNP
start: 73429849
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1000029940
seq_region_name: 17
source: dbSNP
start: 73429852
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1311590548
seq_region_name: 17
source: dbSNP
start: 73429853
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429856
feature_type: variation
id: rs2063312227
seq_region_name: 17
source: dbSNP
start: 73429856
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429858
feature_type: variation
id: rs1029331844
seq_region_name: 17
source: dbSNP
start: 73429858
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429859
feature_type: variation
id: rs1227047904
seq_region_name: 17
source: dbSNP
start: 73429859
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063312281
seq_region_name: 17
source: dbSNP
start: 73429861
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063312294
seq_region_name: 17
source: dbSNP
start: 73429862
strand: 1
-
alleles:
- C
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- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1017963118
seq_region_name: 17
source: dbSNP
start: 73429870
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429876
feature_type: variation
id: rs965078092
seq_region_name: 17
source: dbSNP
start: 73429876
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429879
feature_type: variation
id: rs2063312376
seq_region_name: 17
source: dbSNP
start: 73429879
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063312397
seq_region_name: 17
source: dbSNP
start: 73429880
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429882
feature_type: variation
id: rs2063312415
seq_region_name: 17
source: dbSNP
start: 73429882
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429883
feature_type: variation
id: rs2063312435
seq_region_name: 17
source: dbSNP
start: 73429883
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs976496054
seq_region_name: 17
source: dbSNP
start: 73429885
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429887
feature_type: variation
id: rs2063312472
seq_region_name: 17
source: dbSNP
start: 73429887
strand: 1
-
alleles:
- TTTT
- TTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429890
feature_type: variation
id: rs201989798
seq_region_name: 17
source: dbSNP
start: 73429887
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429890
feature_type: variation
id: rs2063312524
seq_region_name: 17
source: dbSNP
start: 73429890
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429895
feature_type: variation
id: rs1158615919
seq_region_name: 17
source: dbSNP
start: 73429895
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429902
feature_type: variation
id: rs2063312544
seq_region_name: 17
source: dbSNP
start: 73429902
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429905
feature_type: variation
id: rs1212532968
seq_region_name: 17
source: dbSNP
start: 73429905
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429907
feature_type: variation
id: rs1420861065
seq_region_name: 17
source: dbSNP
start: 73429907
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429908
feature_type: variation
id: rs888945049
seq_region_name: 17
source: dbSNP
start: 73429908
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429909
feature_type: variation
id: rs1009183607
seq_region_name: 17
source: dbSNP
start: 73429909
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429922
feature_type: variation
id: rs1568400689
seq_region_name: 17
source: dbSNP
start: 73429922
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429925
feature_type: variation
id: rs2063312632
seq_region_name: 17
source: dbSNP
start: 73429925
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429926
feature_type: variation
id: rs2063312653
seq_region_name: 17
source: dbSNP
start: 73429926
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429932
feature_type: variation
id: rs2063312675
seq_region_name: 17
source: dbSNP
start: 73429932
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429933
feature_type: variation
id: rs1471489455
seq_region_name: 17
source: dbSNP
start: 73429933
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73429940
feature_type: variation
id: rs2145605292
seq_region_name: 17
source: dbSNP
start: 73429940
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73430171
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73430174
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73430177
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
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-
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73430253
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73430301
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430315
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73430317
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73430323
strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
start: 73430325
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73430328
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73430330
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73430335
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs188751064
seq_region_name: 17
source: dbSNP
start: 73430345
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430345
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430346
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1599558770
seq_region_name: 17
source: dbSNP
start: 73430346
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430347
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430348
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1049156267
seq_region_name: 17
source: dbSNP
start: 73430349
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430350
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1765025614
seq_region_name: 17
source: dbSNP
start: 73430353
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063316402
seq_region_name: 17
source: dbSNP
start: 73430360
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063316423
seq_region_name: 17
source: dbSNP
start: 73430361
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430362
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73430367
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430368
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1300698705
seq_region_name: 17
source: dbSNP
start: 73430368
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063316521
seq_region_name: 17
source: dbSNP
start: 73430369
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063316546
seq_region_name: 17
source: dbSNP
start: 73430370
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs889283061
seq_region_name: 17
source: dbSNP
start: 73430376
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430379
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1175491528
seq_region_name: 17
source: dbSNP
start: 73430383
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs774000225
seq_region_name: 17
source: dbSNP
start: 73430384
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063316656
seq_region_name: 17
source: dbSNP
start: 73430386
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1417807061
seq_region_name: 17
source: dbSNP
start: 73430387
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73430388
feature_type: variation
id: rs2063316714
seq_region_name: 17
source: dbSNP
start: 73430388
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430389
feature_type: variation
id: rs2063316740
seq_region_name: 17
source: dbSNP
start: 73430388
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145606294
seq_region_name: 17
source: dbSNP
start: 73430391
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063316764
seq_region_name: 17
source: dbSNP
start: 73430394
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1002306682
seq_region_name: 17
source: dbSNP
start: 73430396
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430399
feature_type: variation
id: rs2063316809
seq_region_name: 17
source: dbSNP
start: 73430399
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430403
feature_type: variation
id: rs1034071998
seq_region_name: 17
source: dbSNP
start: 73430403
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430404
feature_type: variation
id: rs374113891
seq_region_name: 17
source: dbSNP
start: 73430404
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430406
feature_type: variation
id: rs1007755909
seq_region_name: 17
source: dbSNP
start: 73430406
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430410
feature_type: variation
id: rs1599558819
seq_region_name: 17
source: dbSNP
start: 73430410
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430413
feature_type: variation
id: rs1972764296
seq_region_name: 17
source: dbSNP
start: 73430413
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430414
feature_type: variation
id: rs1254408479
seq_region_name: 17
source: dbSNP
start: 73430414
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430416
feature_type: variation
id: rs960740389
seq_region_name: 17
source: dbSNP
start: 73430416
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430418
feature_type: variation
id: rs1013756151
seq_region_name: 17
source: dbSNP
start: 73430418
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430427
feature_type: variation
id: rs1181496181
seq_region_name: 17
source: dbSNP
start: 73430427
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430433
feature_type: variation
id: rs1483807202
seq_region_name: 17
source: dbSNP
start: 73430433
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430436
feature_type: variation
id: rs2063317073
seq_region_name: 17
source: dbSNP
start: 73430436
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430437
feature_type: variation
id: rs2063317093
seq_region_name: 17
source: dbSNP
start: 73430437
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430439
feature_type: variation
id: rs2063317122
seq_region_name: 17
source: dbSNP
start: 73430439
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430441
feature_type: variation
id: rs140713113
seq_region_name: 17
source: dbSNP
start: 73430441
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430442
feature_type: variation
id: rs1021196221
seq_region_name: 17
source: dbSNP
start: 73430442
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430445
feature_type: variation
id: rs2063317204
seq_region_name: 17
source: dbSNP
start: 73430445
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430449
feature_type: variation
id: rs1599558845
seq_region_name: 17
source: dbSNP
start: 73430449
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430451
feature_type: variation
id: rs902110463
seq_region_name: 17
source: dbSNP
start: 73430451
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430452
feature_type: variation
id: rs1881332121
seq_region_name: 17
source: dbSNP
start: 73430452
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430454
feature_type: variation
id: rs2145606415
seq_region_name: 17
source: dbSNP
start: 73430454
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430457
feature_type: variation
id: rs1318191792
seq_region_name: 17
source: dbSNP
start: 73430457
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430458
feature_type: variation
id: rs2063317297
seq_region_name: 17
source: dbSNP
start: 73430458
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430461
feature_type: variation
id: rs1310188586
seq_region_name: 17
source: dbSNP
start: 73430461
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430467
feature_type: variation
id: rs143153761
seq_region_name: 17
source: dbSNP
start: 73430467
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430468
feature_type: variation
id: rs1299858470
seq_region_name: 17
source: dbSNP
start: 73430468
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430470
feature_type: variation
id: rs2063317356
seq_region_name: 17
source: dbSNP
start: 73430470
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430472
feature_type: variation
id: rs776377647
seq_region_name: 17
source: dbSNP
start: 73430472
strand: 1
-
alleles:
- CCCTCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430478
feature_type: variation
id: rs1337943082
seq_region_name: 17
source: dbSNP
start: 73430472
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430474
feature_type: variation
id: rs767036752
seq_region_name: 17
source: dbSNP
start: 73430474
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430475
feature_type: variation
id: rs752063958
seq_region_name: 17
source: dbSNP
start: 73430475
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430475
feature_type: variation
id: rs766366293
seq_region_name: 17
source: dbSNP
start: 73430475
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430476
feature_type: variation
id: rs1369121533
seq_region_name: 17
source: dbSNP
start: 73430476
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430477
feature_type: variation
id: rs371761550
seq_region_name: 17
source: dbSNP
start: 73430477
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430480
feature_type: variation
id: rs759810908
seq_region_name: 17
source: dbSNP
start: 73430480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430481
feature_type: variation
id: rs2063317588
seq_region_name: 17
source: dbSNP
start: 73430481
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430482
feature_type: variation
id: rs1599558891
seq_region_name: 17
source: dbSNP
start: 73430482
strand: 1
-
alleles:
- CC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430486
feature_type: variation
id: rs2063317621
seq_region_name: 17
source: dbSNP
start: 73430485
strand: 1
-
alleles:
- "-"
- CTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430486
feature_type: variation
id: rs1347843749
seq_region_name: 17
source: dbSNP
start: 73430487
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430487
feature_type: variation
id: rs1568400932
seq_region_name: 17
source: dbSNP
start: 73430487
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430488
feature_type: variation
id: rs541151030
seq_region_name: 17
source: dbSNP
start: 73430488
strand: 1
-
alleles:
- GGAG
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430491
feature_type: variation
id: rs1568400942
seq_region_name: 17
source: dbSNP
start: 73430488
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430489
feature_type: variation
id: rs2063317717
seq_region_name: 17
source: dbSNP
start: 73430489
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430490
feature_type: variation
id: rs2063317740
seq_region_name: 17
source: dbSNP
start: 73430490
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430493
feature_type: variation
id: rs1288676841
seq_region_name: 17
source: dbSNP
start: 73430493
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430496
feature_type: variation
id: rs752989741
seq_region_name: 17
source: dbSNP
start: 73430496
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430499
feature_type: variation
id: rs374925795
seq_region_name: 17
source: dbSNP
start: 73430499
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73430504
feature_type: variation
id: rs368560811
seq_region_name: 17
source: dbSNP
start: 73430504
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73430506
feature_type: variation
id: rs1479063828
seq_region_name: 17
source: dbSNP
start: 73430506
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_variant
end: 73430510
feature_type: variation
id: rs2063317889
seq_region_name: 17
source: dbSNP
start: 73430510
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430513
feature_type: variation
id: rs756487634
seq_region_name: 17
source: dbSNP
start: 73430513
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430515
feature_type: variation
id: rs2063317956
seq_region_name: 17
source: dbSNP
start: 73430515
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430516
feature_type: variation
id: rs2063317991
seq_region_name: 17
source: dbSNP
start: 73430516
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: missense_variant
end: 73430517
feature_type: variation
id: rs1105353
seq_region_name: 17
source: dbSNP
start: 73430517
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430518
feature_type: variation
id: rs1420242384
seq_region_name: 17
source: dbSNP
start: 73430518
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430519
feature_type: variation
id: rs2145606662
seq_region_name: 17
source: dbSNP
start: 73430519
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430521
feature_type: variation
id: rs1420291734
seq_region_name: 17
source: dbSNP
start: 73430521
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430522
feature_type: variation
id: rs2145606680
seq_region_name: 17
source: dbSNP
start: 73430522
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430523
feature_type: variation
id: rs144668928
seq_region_name: 17
source: dbSNP
start: 73430523
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73430524
feature_type: variation
id: rs958763262
seq_region_name: 17
source: dbSNP
start: 73430524
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430525
feature_type: variation
id: rs757837217
seq_region_name: 17
source: dbSNP
start: 73430525
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430526
feature_type: variation
id: rs778260753
seq_region_name: 17
source: dbSNP
start: 73430526
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430527
feature_type: variation
id: rs1323834138
seq_region_name: 17
source: dbSNP
start: 73430527
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430528
feature_type: variation
id: rs546473839
seq_region_name: 17
source: dbSNP
start: 73430528
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430530
feature_type: variation
id: rs866880614
seq_region_name: 17
source: dbSNP
start: 73430530
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance:
- benign
consequence_type: missense_variant
end: 73430531
feature_type: variation
id: rs1105354
seq_region_name: 17
source: dbSNP
start: 73430531
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430533
feature_type: variation
id: rs779637691
seq_region_name: 17
source: dbSNP
start: 73430533
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430535
feature_type: variation
id: rs2063318444
seq_region_name: 17
source: dbSNP
start: 73430535
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance:
- likely benign
consequence_type: synonymous_variant
end: 73430540
feature_type: variation
id: rs746680495
seq_region_name: 17
source: dbSNP
start: 73430540
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430541
feature_type: variation
id: rs1311839083
seq_region_name: 17
source: dbSNP
start: 73430541
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430542
feature_type: variation
id: rs768271261
seq_region_name: 17
source: dbSNP
start: 73430542
strand: 1
-
alleles:
- CGC
- CGCGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73430544
feature_type: variation
id: rs759992478
seq_region_name: 17
source: dbSNP
start: 73430542
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430543
feature_type: variation
id: rs776557649
seq_region_name: 17
source: dbSNP
start: 73430543
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430546
feature_type: variation
id: rs748023781
seq_region_name: 17
source: dbSNP
start: 73430546
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430548
feature_type: variation
id: rs2063318671
seq_region_name: 17
source: dbSNP
start: 73430548
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430549
feature_type: variation
id: rs1453586603
seq_region_name: 17
source: dbSNP
start: 73430549
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430552
feature_type: variation
id: rs769819217
seq_region_name: 17
source: dbSNP
start: 73430552
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430553
feature_type: variation
id: rs1252526289
seq_region_name: 17
source: dbSNP
start: 73430553
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430557
feature_type: variation
id: rs1440165607
seq_region_name: 17
source: dbSNP
start: 73430557
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430559
feature_type: variation
id: rs2063318790
seq_region_name: 17
source: dbSNP
start: 73430559
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430564
feature_type: variation
id: rs1180444956
seq_region_name: 17
source: dbSNP
start: 73430564
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430567
feature_type: variation
id: rs774542428
seq_region_name: 17
source: dbSNP
start: 73430567
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73430577
feature_type: variation
id: rs1469466746
seq_region_name: 17
source: dbSNP
start: 73430577
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430579
feature_type: variation
id: rs1163669036
seq_region_name: 17
source: dbSNP
start: 73430579
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430583
feature_type: variation
id: rs2063318881
seq_region_name: 17
source: dbSNP
start: 73430583
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73430587
feature_type: variation
id: rs529082600
seq_region_name: 17
source: dbSNP
start: 73430587
strand: 1
-
alleles:
- GGGGGGG
- GGGGGG
- GGGGGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73430593
feature_type: variation
id: rs753108327
seq_region_name: 17
source: dbSNP
start: 73430587
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73430588
feature_type: variation
id: rs1403308362
seq_region_name: 17
source: dbSNP
start: 73430588
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430589
feature_type: variation
id: rs1323830193
seq_region_name: 17
source: dbSNP
start: 73430589
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73430590
feature_type: variation
id: rs1324632270
seq_region_name: 17
source: dbSNP
start: 73430590
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
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feature_type: variation
id: rs1448096849
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source: dbSNP
start: 73430597
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1333984804
seq_region_name: 17
source: dbSNP
start: 73430601
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs919200073
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source: dbSNP
start: 73430603
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs775786137
seq_region_name: 17
source: dbSNP
start: 73430604
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance:
- uncertain significance
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feature_type: variation
id: rs1285212622
seq_region_name: 17
source: dbSNP
start: 73430605
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1358729984
seq_region_name: 17
source: dbSNP
start: 73430606
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
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id: rs192403239
seq_region_name: 17
source: dbSNP
start: 73430609
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs142879513
seq_region_name: 17
source: dbSNP
start: 73430610
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1458289398
seq_region_name: 17
source: dbSNP
start: 73430611
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063319324
seq_region_name: 17
source: dbSNP
start: 73430613
strand: 1
-
alleles:
- AGATACAGCGGAGACAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs2145607062
seq_region_name: 17
source: dbSNP
start: 73430619
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs2145607075
seq_region_name: 17
source: dbSNP
start: 73430620
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
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feature_type: variation
id: rs2063319364
seq_region_name: 17
source: dbSNP
start: 73430621
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs199972374
seq_region_name: 17
source: dbSNP
start: 73430623
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs887634530
seq_region_name: 17
source: dbSNP
start: 73430625
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs532860570
seq_region_name: 17
source: dbSNP
start: 73430627
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs549573235
seq_region_name: 17
source: dbSNP
start: 73430628
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
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feature_type: variation
id: rs2063319455
seq_region_name: 17
source: dbSNP
start: 73430629
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430631
feature_type: variation
id: rs1431976791
seq_region_name: 17
source: dbSNP
start: 73430631
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430638
feature_type: variation
id: rs750954130
seq_region_name: 17
source: dbSNP
start: 73430638
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430639
feature_type: variation
id: rs1370046344
seq_region_name: 17
source: dbSNP
start: 73430639
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430640
feature_type: variation
id: rs757849775
seq_region_name: 17
source: dbSNP
start: 73430640
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430643
feature_type: variation
id: rs2063319565
seq_region_name: 17
source: dbSNP
start: 73430643
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430647
feature_type: variation
id: rs1163783561
seq_region_name: 17
source: dbSNP
start: 73430647
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430648
feature_type: variation
id: rs550060753
seq_region_name: 17
source: dbSNP
start: 73430648
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1466700555
seq_region_name: 17
source: dbSNP
start: 73430649
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430653
feature_type: variation
id: rs2063319661
seq_region_name: 17
source: dbSNP
start: 73430653
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1167975242
seq_region_name: 17
source: dbSNP
start: 73430654
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430657
feature_type: variation
id: rs936057877
seq_region_name: 17
source: dbSNP
start: 73430657
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430659
feature_type: variation
id: rs377609014
seq_region_name: 17
source: dbSNP
start: 73430659
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430660
feature_type: variation
id: rs746662086
seq_region_name: 17
source: dbSNP
start: 73430660
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs896471018
seq_region_name: 17
source: dbSNP
start: 73430661
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430662
feature_type: variation
id: rs754719353
seq_region_name: 17
source: dbSNP
start: 73430662
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430667
feature_type: variation
id: rs1196334246
seq_region_name: 17
source: dbSNP
start: 73430667
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1226911901
seq_region_name: 17
source: dbSNP
start: 73430668
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1270577067
seq_region_name: 17
source: dbSNP
start: 73430669
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063319913
seq_region_name: 17
source: dbSNP
start: 73430671
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73430672
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063319951
seq_region_name: 17
source: dbSNP
start: 73430674
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063319973
seq_region_name: 17
source: dbSNP
start: 73430677
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs551412617
seq_region_name: 17
source: dbSNP
start: 73430678
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430679
feature_type: variation
id: rs1599559172
seq_region_name: 17
source: dbSNP
start: 73430679
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430685
feature_type: variation
id: rs2063320026
seq_region_name: 17
source: dbSNP
start: 73430685
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs990623529
seq_region_name: 17
source: dbSNP
start: 73430686
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430687
feature_type: variation
id: rs1013577557
seq_region_name: 17
source: dbSNP
start: 73430687
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063320094
seq_region_name: 17
source: dbSNP
start: 73430689
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430700
feature_type: variation
id: rs1441823253
seq_region_name: 17
source: dbSNP
start: 73430696
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430702
feature_type: variation
id: rs754091168
seq_region_name: 17
source: dbSNP
start: 73430702
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430703
feature_type: variation
id: rs1040583984
seq_region_name: 17
source: dbSNP
start: 73430703
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430705
feature_type: variation
id: rs902058209
seq_region_name: 17
source: dbSNP
start: 73430705
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430706
feature_type: variation
id: rs2063320216
seq_region_name: 17
source: dbSNP
start: 73430706
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430711
feature_type: variation
id: rs2063320241
seq_region_name: 17
source: dbSNP
start: 73430711
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430713
feature_type: variation
id: rs2063320260
seq_region_name: 17
source: dbSNP
start: 73430713
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430717
feature_type: variation
id: rs1397428009
seq_region_name: 17
source: dbSNP
start: 73430717
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430720
feature_type: variation
id: rs2063320304
seq_region_name: 17
source: dbSNP
start: 73430720
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430724
feature_type: variation
id: rs1021142220
seq_region_name: 17
source: dbSNP
start: 73430724
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430725
feature_type: variation
id: rs1464804463
seq_region_name: 17
source: dbSNP
start: 73430725
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430726
feature_type: variation
id: rs566462648
seq_region_name: 17
source: dbSNP
start: 73430726
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430728
feature_type: variation
id: rs1377618281
seq_region_name: 17
source: dbSNP
start: 73430728
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430732
feature_type: variation
id: rs2063320396
seq_region_name: 17
source: dbSNP
start: 73430732
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430740
feature_type: variation
id: rs1599559214
seq_region_name: 17
source: dbSNP
start: 73430740
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430743
feature_type: variation
id: rs1790001109
seq_region_name: 17
source: dbSNP
start: 73430743
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430749
feature_type: variation
id: rs2063320427
seq_region_name: 17
source: dbSNP
start: 73430749
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430752
feature_type: variation
id: rs1272537824
seq_region_name: 17
source: dbSNP
start: 73430752
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430753
feature_type: variation
id: rs535370054
seq_region_name: 17
source: dbSNP
start: 73430753
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430754
feature_type: variation
id: rs755398570
seq_region_name: 17
source: dbSNP
start: 73430754
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430760
feature_type: variation
id: rs2063320525
seq_region_name: 17
source: dbSNP
start: 73430760
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430761
feature_type: variation
id: rs2063320549
seq_region_name: 17
source: dbSNP
start: 73430761
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430762
feature_type: variation
id: rs2145607411
seq_region_name: 17
source: dbSNP
start: 73430762
strand: 1
-
alleles:
- GGGG
- GGGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430766
feature_type: variation
id: rs2063320584
seq_region_name: 17
source: dbSNP
start: 73430763
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430766
feature_type: variation
id: rs751946432
seq_region_name: 17
source: dbSNP
start: 73430766
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430769
feature_type: variation
id: rs2063320622
seq_region_name: 17
source: dbSNP
start: 73430769
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430771
feature_type: variation
id: rs1436896563
seq_region_name: 17
source: dbSNP
start: 73430771
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430779
feature_type: variation
id: rs2063320669
seq_region_name: 17
source: dbSNP
start: 73430779
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430791
feature_type: variation
id: rs2063320689
seq_region_name: 17
source: dbSNP
start: 73430791
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430792
feature_type: variation
id: rs2063320712
seq_region_name: 17
source: dbSNP
start: 73430792
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430798
feature_type: variation
id: rs1048008933
seq_region_name: 17
source: dbSNP
start: 73430798
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430803
feature_type: variation
id: rs954246627
seq_region_name: 17
source: dbSNP
start: 73430803
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430805
feature_type: variation
id: rs1197354195
seq_region_name: 17
source: dbSNP
start: 73430805
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430811
feature_type: variation
id: rs2063320775
seq_region_name: 17
source: dbSNP
start: 73430811
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430812
feature_type: variation
id: rs2063320800
seq_region_name: 17
source: dbSNP
start: 73430812
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430816
feature_type: variation
id: rs1342605425
seq_region_name: 17
source: dbSNP
start: 73430816
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430818
feature_type: variation
id: rs2063320835
seq_region_name: 17
source: dbSNP
start: 73430818
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73430819
feature_type: variation
id: rs2063320859
seq_region_name: 17
source: dbSNP
start: 73430819
strand: 1
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73431042
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73431044
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73431045
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73431076
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73431085
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431089
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431096
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73431098
strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431102
strand: 1
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alleles:
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- T
assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431105
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431108
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431111
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431116
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431121
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431125
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73431129
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431126
strand: 1
-
alleles:
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- G
- T
assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs777681323
seq_region_name: 17
source: dbSNP
start: 73431130
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs575713340
seq_region_name: 17
source: dbSNP
start: 73431131
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs888063910
seq_region_name: 17
source: dbSNP
start: 73431140
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1032631434
seq_region_name: 17
source: dbSNP
start: 73431143
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063322764
seq_region_name: 17
source: dbSNP
start: 73431144
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1280369636
seq_region_name: 17
source: dbSNP
start: 73431146
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs370231780
seq_region_name: 17
source: dbSNP
start: 73431147
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063322836
seq_region_name: 17
source: dbSNP
start: 73431150
strand: 1
-
alleles:
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- AGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1403035472
seq_region_name: 17
source: dbSNP
start: 73431155
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063322853
seq_region_name: 17
source: dbSNP
start: 73431160
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs115298444
seq_region_name: 17
source: dbSNP
start: 73431161
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs557763518
seq_region_name: 17
source: dbSNP
start: 73431162
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063322919
seq_region_name: 17
source: dbSNP
start: 73431167
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063322937
seq_region_name: 17
source: dbSNP
start: 73431168
strand: 1
-
alleles:
- CACACA
- CACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431175
feature_type: variation
id: rs2063322956
seq_region_name: 17
source: dbSNP
start: 73431170
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431171
feature_type: variation
id: rs2063322972
seq_region_name: 17
source: dbSNP
start: 73431171
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063322991
seq_region_name: 17
source: dbSNP
start: 73431172
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431173
feature_type: variation
id: rs2063323007
seq_region_name: 17
source: dbSNP
start: 73431173
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs965757564
seq_region_name: 17
source: dbSNP
start: 73431174
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431175
feature_type: variation
id: rs2063323045
seq_region_name: 17
source: dbSNP
start: 73431175
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431176
feature_type: variation
id: rs373377092
seq_region_name: 17
source: dbSNP
start: 73431176
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431186
feature_type: variation
id: rs2063323095
seq_region_name: 17
source: dbSNP
start: 73431186
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063323116
seq_region_name: 17
source: dbSNP
start: 73431197
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431200
feature_type: variation
id: rs1185669757
seq_region_name: 17
source: dbSNP
start: 73431200
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431202
feature_type: variation
id: rs1475720775
seq_region_name: 17
source: dbSNP
start: 73431202
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431204
feature_type: variation
id: rs2063323189
seq_region_name: 17
source: dbSNP
start: 73431204
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431212
feature_type: variation
id: rs2063323216
seq_region_name: 17
source: dbSNP
start: 73431212
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431216
feature_type: variation
id: rs1243710274
seq_region_name: 17
source: dbSNP
start: 73431216
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431217
feature_type: variation
id: rs563904167
seq_region_name: 17
source: dbSNP
start: 73431217
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431219
feature_type: variation
id: rs139374314
seq_region_name: 17
source: dbSNP
start: 73431219
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431220
feature_type: variation
id: rs561639848
seq_region_name: 17
source: dbSNP
start: 73431220
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431228
feature_type: variation
id: rs1274117289
seq_region_name: 17
source: dbSNP
start: 73431228
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431232
feature_type: variation
id: rs1012613280
seq_region_name: 17
source: dbSNP
start: 73431232
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431233
feature_type: variation
id: rs950370381
seq_region_name: 17
source: dbSNP
start: 73431233
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431235
feature_type: variation
id: rs2063323379
seq_region_name: 17
source: dbSNP
start: 73431235
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431236
feature_type: variation
id: rs2063323395
seq_region_name: 17
source: dbSNP
start: 73431236
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431237
feature_type: variation
id: rs985105018
seq_region_name: 17
source: dbSNP
start: 73431237
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431238
feature_type: variation
id: rs909170988
seq_region_name: 17
source: dbSNP
start: 73431238
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431239
feature_type: variation
id: rs1364710262
seq_region_name: 17
source: dbSNP
start: 73431239
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431243
feature_type: variation
id: rs529128743
seq_region_name: 17
source: dbSNP
start: 73431243
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431246
feature_type: variation
id: rs998727822
seq_region_name: 17
source: dbSNP
start: 73431246
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431248
feature_type: variation
id: rs2145608253
seq_region_name: 17
source: dbSNP
start: 73431248
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431254
feature_type: variation
id: rs2063323511
seq_region_name: 17
source: dbSNP
start: 73431254
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431257
feature_type: variation
id: rs544417622
seq_region_name: 17
source: dbSNP
start: 73431257
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431260
feature_type: variation
id: rs937822204
seq_region_name: 17
source: dbSNP
start: 73431260
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431261
feature_type: variation
id: rs112530467
seq_region_name: 17
source: dbSNP
start: 73431261
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431265
feature_type: variation
id: rs75879140
seq_region_name: 17
source: dbSNP
start: 73431265
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431276
feature_type: variation
id: rs372082706
seq_region_name: 17
source: dbSNP
start: 73431276
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431279
feature_type: variation
id: rs1042461562
seq_region_name: 17
source: dbSNP
start: 73431279
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431280
feature_type: variation
id: rs976161041
seq_region_name: 17
source: dbSNP
start: 73431280
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431284
feature_type: variation
id: rs1350836896
seq_region_name: 17
source: dbSNP
start: 73431284
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431286
feature_type: variation
id: rs2063323718
seq_region_name: 17
source: dbSNP
start: 73431286
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431288
feature_type: variation
id: rs781694099
seq_region_name: 17
source: dbSNP
start: 73431288
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431291
feature_type: variation
id: rs191677381
seq_region_name: 17
source: dbSNP
start: 73431291
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431292
feature_type: variation
id: rs2063323776
seq_region_name: 17
source: dbSNP
start: 73431292
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431293
feature_type: variation
id: rs1599559586
seq_region_name: 17
source: dbSNP
start: 73431293
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431296
feature_type: variation
id: rs923937295
seq_region_name: 17
source: dbSNP
start: 73431296
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431298
feature_type: variation
id: rs150026168
seq_region_name: 17
source: dbSNP
start: 73431298
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431299
feature_type: variation
id: rs145410943
seq_region_name: 17
source: dbSNP
start: 73431299
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431300
feature_type: variation
id: rs2063323892
seq_region_name: 17
source: dbSNP
start: 73431300
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431302
feature_type: variation
id: rs1599559604
seq_region_name: 17
source: dbSNP
start: 73431302
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431315
feature_type: variation
id: rs2063323943
seq_region_name: 17
source: dbSNP
start: 73431315
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431318
feature_type: variation
id: rs1599559609
seq_region_name: 17
source: dbSNP
start: 73431318
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431319
feature_type: variation
id: rs890072593
seq_region_name: 17
source: dbSNP
start: 73431319
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431321
feature_type: variation
id: rs2063324005
seq_region_name: 17
source: dbSNP
start: 73431321
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431322
feature_type: variation
id: rs1233423424
seq_region_name: 17
source: dbSNP
start: 73431322
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431323
feature_type: variation
id: rs2063324045
seq_region_name: 17
source: dbSNP
start: 73431323
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431325
feature_type: variation
id: rs1276074738
seq_region_name: 17
source: dbSNP
start: 73431325
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431327
feature_type: variation
id: rs2063324070
seq_region_name: 17
source: dbSNP
start: 73431327
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431329
feature_type: variation
id: rs1195534475
seq_region_name: 17
source: dbSNP
start: 73431329
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431331
feature_type: variation
id: rs1345323955
seq_region_name: 17
source: dbSNP
start: 73431331
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431333
feature_type: variation
id: rs2063324134
seq_region_name: 17
source: dbSNP
start: 73431333
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431340
feature_type: variation
id: rs2063324149
seq_region_name: 17
source: dbSNP
start: 73431340
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431354
feature_type: variation
id: rs2063324169
seq_region_name: 17
source: dbSNP
start: 73431354
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431362
feature_type: variation
id: rs1456612677
seq_region_name: 17
source: dbSNP
start: 73431362
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431364
feature_type: variation
id: rs2063324208
seq_region_name: 17
source: dbSNP
start: 73431364
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431365
feature_type: variation
id: rs2063324234
seq_region_name: 17
source: dbSNP
start: 73431365
strand: 1
-
alleles:
- GACTGGGACAGAC
- GAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431378
feature_type: variation
id: rs1232454051
seq_region_name: 17
source: dbSNP
start: 73431366
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431369
feature_type: variation
id: rs1205728290
seq_region_name: 17
source: dbSNP
start: 73431369
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431372
feature_type: variation
id: rs1209658338
seq_region_name: 17
source: dbSNP
start: 73431372
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431373
feature_type: variation
id: rs2063324334
seq_region_name: 17
source: dbSNP
start: 73431373
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431379
feature_type: variation
id: rs2063324353
seq_region_name: 17
source: dbSNP
start: 73431379
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431386
feature_type: variation
id: rs2145608493
seq_region_name: 17
source: dbSNP
start: 73431386
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431388
feature_type: variation
id: rs1309625446
seq_region_name: 17
source: dbSNP
start: 73431388
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431394
feature_type: variation
id: rs1280072778
seq_region_name: 17
source: dbSNP
start: 73431394
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431396
feature_type: variation
id: rs2063324416
seq_region_name: 17
source: dbSNP
start: 73431396
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431397
feature_type: variation
id: rs1599559641
seq_region_name: 17
source: dbSNP
start: 73431397
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431401
feature_type: variation
id: rs140156617
seq_region_name: 17
source: dbSNP
start: 73431401
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431402
feature_type: variation
id: rs1451610262
seq_region_name: 17
source: dbSNP
start: 73431402
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431404
feature_type: variation
id: rs2063324495
seq_region_name: 17
source: dbSNP
start: 73431404
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431405
feature_type: variation
id: rs1349173767
seq_region_name: 17
source: dbSNP
start: 73431405
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431412
feature_type: variation
id: rs2063324543
seq_region_name: 17
source: dbSNP
start: 73431412
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431415
feature_type: variation
id: rs568742295
seq_region_name: 17
source: dbSNP
start: 73431415
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431416
feature_type: variation
id: rs1599559658
seq_region_name: 17
source: dbSNP
start: 73431416
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431417
feature_type: variation
id: rs1041195505
seq_region_name: 17
source: dbSNP
start: 73431417
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431418
feature_type: variation
id: rs535747861
seq_region_name: 17
source: dbSNP
start: 73431418
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431422
feature_type: variation
id: rs2063324631
seq_region_name: 17
source: dbSNP
start: 73431422
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431429
feature_type: variation
id: rs1055820530
seq_region_name: 17
source: dbSNP
start: 73431429
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431438
feature_type: variation
id: rs75873846
seq_region_name: 17
source: dbSNP
start: 73431438
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431440
feature_type: variation
id: rs749020665
seq_region_name: 17
source: dbSNP
start: 73431440
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431445
feature_type: variation
id: rs1026102107
seq_region_name: 17
source: dbSNP
start: 73431445
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431447
feature_type: variation
id: rs950357907
seq_region_name: 17
source: dbSNP
start: 73431447
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431451
feature_type: variation
id: rs2063324772
seq_region_name: 17
source: dbSNP
start: 73431451
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431455
feature_type: variation
id: rs367822976
seq_region_name: 17
source: dbSNP
start: 73431455
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431456
feature_type: variation
id: rs2063324818
seq_region_name: 17
source: dbSNP
start: 73431456
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431457
feature_type: variation
id: rs1292942377
seq_region_name: 17
source: dbSNP
start: 73431457
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431459
feature_type: variation
id: rs371659065
seq_region_name: 17
source: dbSNP
start: 73431459
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431460
feature_type: variation
id: rs769499426
seq_region_name: 17
source: dbSNP
start: 73431460
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431463
feature_type: variation
id: rs2063324908
seq_region_name: 17
source: dbSNP
start: 73431463
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431467
feature_type: variation
id: rs773225709
seq_region_name: 17
source: dbSNP
start: 73431467
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431469
feature_type: variation
id: rs1338666982
seq_region_name: 17
source: dbSNP
start: 73431469
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431472
feature_type: variation
id: rs749241011
seq_region_name: 17
source: dbSNP
start: 73431472
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431473
feature_type: variation
id: rs1257946682
seq_region_name: 17
source: dbSNP
start: 73431473
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431474
feature_type: variation
id: rs772272331
seq_region_name: 17
source: dbSNP
start: 73431474
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431475
feature_type: variation
id: rs1798920704
seq_region_name: 17
source: dbSNP
start: 73431475
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431479
feature_type: variation
id: rs775767743
seq_region_name: 17
source: dbSNP
start: 73431479
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431480
feature_type: variation
id: rs1426404079
seq_region_name: 17
source: dbSNP
start: 73431480
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431481
feature_type: variation
id: rs764413908
seq_region_name: 17
source: dbSNP
start: 73431481
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431487
feature_type: variation
id: rs776745161
seq_region_name: 17
source: dbSNP
start: 73431487
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431488
feature_type: variation
id: rs762192843
seq_region_name: 17
source: dbSNP
start: 73431488
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431492
feature_type: variation
id: rs1372004193
seq_region_name: 17
source: dbSNP
start: 73431492
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431493
feature_type: variation
id: rs906977164
seq_region_name: 17
source: dbSNP
start: 73431493
strand: 1
-
alleles:
- CACAC
- CAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73431497
feature_type: variation
id: rs1164850702
seq_region_name: 17
source: dbSNP
start: 73431493
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73431497
feature_type: variation
id: rs1250155531
seq_region_name: 17
source: dbSNP
start: 73431497
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73431504
feature_type: variation
id: rs2063325284
seq_region_name: 17
source: dbSNP
start: 73431504
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431506
feature_type: variation
id: rs2063325316
seq_region_name: 17
source: dbSNP
start: 73431506
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73431508
feature_type: variation
id: rs376227214
seq_region_name: 17
source: dbSNP
start: 73431508
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431509
feature_type: variation
id: rs151082679
seq_region_name: 17
source: dbSNP
start: 73431509
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431510
feature_type: variation
id: rs1163442687
seq_region_name: 17
source: dbSNP
start: 73431510
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431511
feature_type: variation
id: rs758973579
seq_region_name: 17
source: dbSNP
start: 73431511
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431513
feature_type: variation
id: rs2063325452
seq_region_name: 17
source: dbSNP
start: 73431513
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431516
feature_type: variation
id: rs2063325482
seq_region_name: 17
source: dbSNP
start: 73431516
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431525
feature_type: variation
id: rs1383847340
seq_region_name: 17
source: dbSNP
start: 73431525
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431526
feature_type: variation
id: rs2063325536
seq_region_name: 17
source: dbSNP
start: 73431526
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431527
feature_type: variation
id: rs141061660
seq_region_name: 17
source: dbSNP
start: 73431527
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431532
feature_type: variation
id: rs199755742
seq_region_name: 17
source: dbSNP
start: 73431532
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431533
feature_type: variation
id: rs754556933
seq_region_name: 17
source: dbSNP
start: 73431533
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431535
feature_type: variation
id: rs747769635
seq_region_name: 17
source: dbSNP
start: 73431535
strand: 1
-
alleles:
- CCCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73431540
feature_type: variation
id: rs1402156566
seq_region_name: 17
source: dbSNP
start: 73431535
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431536
feature_type: variation
id: rs1325947872
seq_region_name: 17
source: dbSNP
start: 73431536
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73431540
feature_type: variation
id: rs755870843
seq_region_name: 17
source: dbSNP
start: 73431540
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431541
feature_type: variation
id: rs756850845
seq_region_name: 17
source: dbSNP
start: 73431541
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431543
feature_type: variation
id: rs2063325856
seq_region_name: 17
source: dbSNP
start: 73431543
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431545
feature_type: variation
id: rs2063325882
seq_region_name: 17
source: dbSNP
start: 73431545
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431549
feature_type: variation
id: rs917708678
seq_region_name: 17
source: dbSNP
start: 73431549
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431550
feature_type: variation
id: rs557827176
seq_region_name: 17
source: dbSNP
start: 73431550
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431555
feature_type: variation
id: rs749222687
seq_region_name: 17
source: dbSNP
start: 73431555
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431556
feature_type: variation
id: rs1286552658
seq_region_name: 17
source: dbSNP
start: 73431556
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431557
feature_type: variation
id: rs771037981
seq_region_name: 17
source: dbSNP
start: 73431557
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431561
feature_type: variation
id: rs978145571
seq_region_name: 17
source: dbSNP
start: 73431561
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431568
feature_type: variation
id: rs780248259
seq_region_name: 17
source: dbSNP
start: 73431568
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431570
feature_type: variation
id: rs1260373231
seq_region_name: 17
source: dbSNP
start: 73431570
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431572
feature_type: variation
id: rs747066948
seq_region_name: 17
source: dbSNP
start: 73431572
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431573
feature_type: variation
id: rs572942777
seq_region_name: 17
source: dbSNP
start: 73431573
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431575
feature_type: variation
id: rs1017570552
seq_region_name: 17
source: dbSNP
start: 73431575
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431577
feature_type: variation
id: rs776859124
seq_region_name: 17
source: dbSNP
start: 73431577
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431578
feature_type: variation
id: rs201337697
seq_region_name: 17
source: dbSNP
start: 73431578
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73431585
feature_type: variation
id: rs997544833
seq_region_name: 17
source: dbSNP
start: 73431585
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431587
feature_type: variation
id: rs2063326301
seq_region_name: 17
source: dbSNP
start: 73431587
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431590
feature_type: variation
id: rs2063326336
seq_region_name: 17
source: dbSNP
start: 73431590
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431592
feature_type: variation
id: rs2063326357
seq_region_name: 17
source: dbSNP
start: 73431592
strand: 1
-
alleles:
- TGATGA
- TGA
assembly_name: GRCh38
clinical_significance: []
consequence_type: inframe_deletion
end: 73431600
feature_type: variation
id: rs1361581803
seq_region_name: 17
source: dbSNP
start: 73431595
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431598
feature_type: variation
id: rs2063326397
seq_region_name: 17
source: dbSNP
start: 73431598
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431599
feature_type: variation
id: rs770142927
seq_region_name: 17
source: dbSNP
start: 73431599
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431601
feature_type: variation
id: rs555447629
seq_region_name: 17
source: dbSNP
start: 73431601
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431611
feature_type: variation
id: rs573893514
seq_region_name: 17
source: dbSNP
start: 73431611
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431612
feature_type: variation
id: rs766912066
seq_region_name: 17
source: dbSNP
start: 73431612
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
- likely benign
consequence_type: missense_variant
end: 73431613
feature_type: variation
id: rs200185560
seq_region_name: 17
source: dbSNP
start: 73431613
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431615
feature_type: variation
id: rs766939997
seq_region_name: 17
source: dbSNP
start: 73431615
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431619
feature_type: variation
id: rs909389141
seq_region_name: 17
source: dbSNP
start: 73431619
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431623
feature_type: variation
id: rs1599559917
seq_region_name: 17
source: dbSNP
start: 73431623
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431624
feature_type: variation
id: rs752387979
seq_region_name: 17
source: dbSNP
start: 73431624
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431626
feature_type: variation
id: rs1309639234
seq_region_name: 17
source: dbSNP
start: 73431626
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431628
feature_type: variation
id: rs755887368
seq_region_name: 17
source: dbSNP
start: 73431628
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431629
feature_type: variation
id: rs1214729319
seq_region_name: 17
source: dbSNP
start: 73431629
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73431630
feature_type: variation
id: rs200893218
seq_region_name: 17
source: dbSNP
start: 73431630
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431631
feature_type: variation
id: rs1259749348
seq_region_name: 17
source: dbSNP
start: 73431631
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431632
feature_type: variation
id: rs1567768585
seq_region_name: 17
source: dbSNP
start: 73431632
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431633
feature_type: variation
id: rs753723834
seq_region_name: 17
source: dbSNP
start: 73431633
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431635
feature_type: variation
id: rs1211095737
seq_region_name: 17
source: dbSNP
start: 73431635
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431637
feature_type: variation
id: rs1215048956
seq_region_name: 17
source: dbSNP
start: 73431637
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431638
feature_type: variation
id: rs1250672842
seq_region_name: 17
source: dbSNP
start: 73431638
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431641
feature_type: variation
id: rs1259661257
seq_region_name: 17
source: dbSNP
start: 73431641
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431644
feature_type: variation
id: rs139041166
seq_region_name: 17
source: dbSNP
start: 73431644
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431645
feature_type: variation
id: rs1567768620
seq_region_name: 17
source: dbSNP
start: 73431645
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431646
feature_type: variation
id: rs1567768623
seq_region_name: 17
source: dbSNP
start: 73431646
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431653
feature_type: variation
id: rs757145368
seq_region_name: 17
source: dbSNP
start: 73431653
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431654
feature_type: variation
id: rs1381259130
seq_region_name: 17
source: dbSNP
start: 73431654
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431661
feature_type: variation
id: rs1567768629
seq_region_name: 17
source: dbSNP
start: 73431661
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73431663
feature_type: variation
id: rs778857817
seq_region_name: 17
source: dbSNP
start: 73431663
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431664
feature_type: variation
id: rs145196996
seq_region_name: 17
source: dbSNP
start: 73431664
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73431665
feature_type: variation
id: rs768718345
seq_region_name: 17
source: dbSNP
start: 73431665
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431667
feature_type: variation
id: rs2063327187
seq_region_name: 17
source: dbSNP
start: 73431667
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73431668
feature_type: variation
id: rs781199730
seq_region_name: 17
source: dbSNP
start: 73431668
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73431669
feature_type: variation
id: rs748390913
seq_region_name: 17
source: dbSNP
start: 73431669
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73431675
feature_type: variation
id: rs372370744
seq_region_name: 17
source: dbSNP
start: 73431675
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73431677
feature_type: variation
id: rs1291042973
seq_region_name: 17
source: dbSNP
start: 73431677
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73431684
feature_type: variation
id: rs2063327314
seq_region_name: 17
source: dbSNP
start: 73431684
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73431685
feature_type: variation
id: rs1392389259
seq_region_name: 17
source: dbSNP
start: 73431685
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73431686
feature_type: variation
id: rs770052929
seq_region_name: 17
source: dbSNP
start: 73431686
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431687
feature_type: variation
id: rs1599560009
seq_region_name: 17
source: dbSNP
start: 73431687
strand: 1
-
alleles:
- GGGGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431692
feature_type: variation
id: rs2063327405
seq_region_name: 17
source: dbSNP
start: 73431688
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431690
feature_type: variation
id: rs2063327421
seq_region_name: 17
source: dbSNP
start: 73431690
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431691
feature_type: variation
id: rs2063327446
seq_region_name: 17
source: dbSNP
start: 73431691
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431693
feature_type: variation
id: rs1599560015
seq_region_name: 17
source: dbSNP
start: 73431693
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431700
feature_type: variation
id: rs763265302
seq_region_name: 17
source: dbSNP
start: 73431700
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431703
feature_type: variation
id: rs1567768669
seq_region_name: 17
source: dbSNP
start: 73431703
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431704
feature_type: variation
id: rs942928064
seq_region_name: 17
source: dbSNP
start: 73431704
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431705
feature_type: variation
id: rs771307960
seq_region_name: 17
source: dbSNP
start: 73431705
strand: 1
-
alleles:
- C
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431706
feature_type: variation
id: rs774854436
seq_region_name: 17
source: dbSNP
start: 73431706
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431710
feature_type: variation
id: rs2145609448
seq_region_name: 17
source: dbSNP
start: 73431710
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431711
feature_type: variation
id: rs760027709
seq_region_name: 17
source: dbSNP
start: 73431711
strand: 1
-
alleles:
- GGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431713
feature_type: variation
id: rs2063327619
seq_region_name: 17
source: dbSNP
start: 73431711
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431713
feature_type: variation
id: rs1380478275
seq_region_name: 17
source: dbSNP
start: 73431713
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431716
feature_type: variation
id: rs1599560041
seq_region_name: 17
source: dbSNP
start: 73431716
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431717
feature_type: variation
id: rs1599560045
seq_region_name: 17
source: dbSNP
start: 73431717
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431718
feature_type: variation
id: rs2063327696
seq_region_name: 17
source: dbSNP
start: 73431718
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431719
feature_type: variation
id: rs767039623
seq_region_name: 17
source: dbSNP
start: 73431719
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431722
feature_type: variation
id: rs562729165
seq_region_name: 17
source: dbSNP
start: 73431722
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431723
feature_type: variation
id: rs375363469
seq_region_name: 17
source: dbSNP
start: 73431723
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431724
feature_type: variation
id: rs901331897
seq_region_name: 17
source: dbSNP
start: 73431724
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431725
feature_type: variation
id: rs1168116307
seq_region_name: 17
source: dbSNP
start: 73431725
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431730
feature_type: variation
id: rs545161564
seq_region_name: 17
source: dbSNP
start: 73431730
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431732
feature_type: variation
id: rs2063327841
seq_region_name: 17
source: dbSNP
start: 73431732
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431733
feature_type: variation
id: rs994374536
seq_region_name: 17
source: dbSNP
start: 73431733
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431734
feature_type: variation
id: rs2063327863
seq_region_name: 17
source: dbSNP
start: 73431734
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431735
feature_type: variation
id: rs1191425902
seq_region_name: 17
source: dbSNP
start: 73431735
strand: 1
-
alleles:
- "-"
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431735
feature_type: variation
id: rs1420446811
seq_region_name: 17
source: dbSNP
start: 73431736
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431736
feature_type: variation
id: rs879724368
seq_region_name: 17
source: dbSNP
start: 73431736
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431739
feature_type: variation
id: rs1047492793
seq_region_name: 17
source: dbSNP
start: 73431739
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431742
feature_type: variation
id: rs2063327979
seq_region_name: 17
source: dbSNP
start: 73431742
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431747
feature_type: variation
id: rs778489152
seq_region_name: 17
source: dbSNP
start: 73431747
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431748
feature_type: variation
id: rs2063328024
seq_region_name: 17
source: dbSNP
start: 73431748
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431754
feature_type: variation
id: rs1186657252
seq_region_name: 17
source: dbSNP
start: 73431754
strand: 1
-
alleles:
- CCCCCC
- CCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431759
feature_type: variation
id: rs2063328054
seq_region_name: 17
source: dbSNP
start: 73431754
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431757
feature_type: variation
id: rs916859550
seq_region_name: 17
source: dbSNP
start: 73431757
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431759
feature_type: variation
id: rs1270924641
seq_region_name: 17
source: dbSNP
start: 73431759
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431762
feature_type: variation
id: rs2063328127
seq_region_name: 17
source: dbSNP
start: 73431762
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431763
feature_type: variation
id: rs1212654273
seq_region_name: 17
source: dbSNP
start: 73431763
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431764
feature_type: variation
id: rs2063328167
seq_region_name: 17
source: dbSNP
start: 73431764
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431765
feature_type: variation
id: rs2063328194
seq_region_name: 17
source: dbSNP
start: 73431765
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431766
feature_type: variation
id: rs886218664
seq_region_name: 17
source: dbSNP
start: 73431766
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431767
feature_type: variation
id: rs2063328261
seq_region_name: 17
source: dbSNP
start: 73431767
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431768
feature_type: variation
id: rs2063328279
seq_region_name: 17
source: dbSNP
start: 73431768
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431781
feature_type: variation
id: rs2063328301
seq_region_name: 17
source: dbSNP
start: 73431781
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431783
feature_type: variation
id: rs571648636
seq_region_name: 17
source: dbSNP
start: 73431783
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431787
feature_type: variation
id: rs369088111
seq_region_name: 17
source: dbSNP
start: 73431787
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431790
feature_type: variation
id: rs2063328356
seq_region_name: 17
source: dbSNP
start: 73431790
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431797
feature_type: variation
id: rs2063328377
seq_region_name: 17
source: dbSNP
start: 73431797
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431801
feature_type: variation
id: rs2063328396
seq_region_name: 17
source: dbSNP
start: 73431801
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431806
feature_type: variation
id: rs527336831
seq_region_name: 17
source: dbSNP
start: 73431806
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431807
feature_type: variation
id: rs373361066
seq_region_name: 17
source: dbSNP
start: 73431807
strand: 1
-
alleles:
- GGTGG
- GG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431811
feature_type: variation
id: rs2063328454
seq_region_name: 17
source: dbSNP
start: 73431807
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431810
feature_type: variation
id: rs2063328477
seq_region_name: 17
source: dbSNP
start: 73431810
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431817
feature_type: variation
id: rs1384062477
seq_region_name: 17
source: dbSNP
start: 73431817
strand: 1
-
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73431823
strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431831
strand: 1
-
alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73431839
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73431844
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431846
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431854
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73431859
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431860
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431875
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431877
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063328985
seq_region_name: 17
source: dbSNP
start: 73431882
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73431883
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431886
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431887
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1338505984
seq_region_name: 17
source: dbSNP
start: 73431896
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431907
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431908
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73431909
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431910
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431915
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431916
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73431918
feature_type: variation
id: rs1302811627
seq_region_name: 17
source: dbSNP
start: 73431918
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063329273
seq_region_name: 17
source: dbSNP
start: 73431920
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431923
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1373537220
seq_region_name: 17
source: dbSNP
start: 73431926
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431927
feature_type: variation
id: rs958126682
seq_region_name: 17
source: dbSNP
start: 73431927
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs867969339
seq_region_name: 17
source: dbSNP
start: 73431934
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431935
feature_type: variation
id: rs2145609984
seq_region_name: 17
source: dbSNP
start: 73431935
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431936
feature_type: variation
id: rs571290663
seq_region_name: 17
source: dbSNP
start: 73431936
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431937
feature_type: variation
id: rs1030339371
seq_region_name: 17
source: dbSNP
start: 73431937
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431940
feature_type: variation
id: rs1433433921
seq_region_name: 17
source: dbSNP
start: 73431940
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431942
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73431942
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431947
feature_type: variation
id: rs2145610021
seq_region_name: 17
source: dbSNP
start: 73431947
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431954
feature_type: variation
id: rs370704716
seq_region_name: 17
source: dbSNP
start: 73431954
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431955
feature_type: variation
id: rs1004967754
seq_region_name: 17
source: dbSNP
start: 73431955
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431959
feature_type: variation
id: rs2063329529
seq_region_name: 17
source: dbSNP
start: 73431955
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431956
feature_type: variation
id: rs2145610048
seq_region_name: 17
source: dbSNP
start: 73431956
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431960
feature_type: variation
id: rs772595082
seq_region_name: 17
source: dbSNP
start: 73431960
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431961
feature_type: variation
id: rs1179192652
seq_region_name: 17
source: dbSNP
start: 73431961
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431963
feature_type: variation
id: rs963565580
seq_region_name: 17
source: dbSNP
start: 73431963
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431964
feature_type: variation
id: rs59498343
seq_region_name: 17
source: dbSNP
start: 73431964
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431973
feature_type: variation
id: rs911192407
seq_region_name: 17
source: dbSNP
start: 73431973
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431976
feature_type: variation
id: rs1023820901
seq_region_name: 17
source: dbSNP
start: 73431976
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431977
feature_type: variation
id: rs1275662571
seq_region_name: 17
source: dbSNP
start: 73431977
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431980
feature_type: variation
id: rs569113282
seq_region_name: 17
source: dbSNP
start: 73431980
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431982
feature_type: variation
id: rs1347171091
seq_region_name: 17
source: dbSNP
start: 73431982
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431986
feature_type: variation
id: rs1278049818
seq_region_name: 17
source: dbSNP
start: 73431986
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431987
feature_type: variation
id: rs182685948
seq_region_name: 17
source: dbSNP
start: 73431987
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431989
feature_type: variation
id: rs539637334
seq_region_name: 17
source: dbSNP
start: 73431989
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431990
feature_type: variation
id: rs879887374
seq_region_name: 17
source: dbSNP
start: 73431990
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431991
feature_type: variation
id: rs930112786
seq_region_name: 17
source: dbSNP
start: 73431991
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431992
feature_type: variation
id: rs143896009
seq_region_name: 17
source: dbSNP
start: 73431992
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431996
feature_type: variation
id: rs1314018945
seq_region_name: 17
source: dbSNP
start: 73431996
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73431999
feature_type: variation
id: rs2063329889
seq_region_name: 17
source: dbSNP
start: 73431999
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432003
feature_type: variation
id: rs1260794432
seq_region_name: 17
source: dbSNP
start: 73432003
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432008
feature_type: variation
id: rs2145610176
seq_region_name: 17
source: dbSNP
start: 73432008
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432014
feature_type: variation
id: rs376377454
seq_region_name: 17
source: dbSNP
start: 73432014
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432017
feature_type: variation
id: rs1599560306
seq_region_name: 17
source: dbSNP
start: 73432017
strand: 1
-
alleles:
- CCC
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432020
feature_type: variation
id: rs2063329998
seq_region_name: 17
source: dbSNP
start: 73432018
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432019
feature_type: variation
id: rs1753349076
seq_region_name: 17
source: dbSNP
start: 73432019
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432020
feature_type: variation
id: rs1166648230
seq_region_name: 17
source: dbSNP
start: 73432020
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432021
feature_type: variation
id: rs988558320
seq_region_name: 17
source: dbSNP
start: 73432021
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432023
feature_type: variation
id: rs2063330065
seq_region_name: 17
source: dbSNP
start: 73432023
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432024
feature_type: variation
id: rs1599560315
seq_region_name: 17
source: dbSNP
start: 73432024
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432025
feature_type: variation
id: rs371496809
seq_region_name: 17
source: dbSNP
start: 73432024
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432025
feature_type: variation
id: rs111864336
seq_region_name: 17
source: dbSNP
start: 73432025
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432028
feature_type: variation
id: rs1390146010
seq_region_name: 17
source: dbSNP
start: 73432028
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432029
feature_type: variation
id: rs1444018158
seq_region_name: 17
source: dbSNP
start: 73432029
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432032
feature_type: variation
id: rs1282281897
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-
alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1599560429
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source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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id: rs2145610525
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73432171
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73432187
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73432197
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73432204
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs964057599
seq_region_name: 17
source: dbSNP
start: 73432205
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1167229979
seq_region_name: 17
source: dbSNP
start: 73432213
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs556172476
seq_region_name: 17
source: dbSNP
start: 73432217
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs765670387
seq_region_name: 17
source: dbSNP
start: 73432220
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73432222
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063331459
seq_region_name: 17
source: dbSNP
start: 73432225
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063331485
seq_region_name: 17
source: dbSNP
start: 73432226
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063331508
seq_region_name: 17
source: dbSNP
start: 73432232
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432234
feature_type: variation
id: rs976775805
seq_region_name: 17
source: dbSNP
start: 73432234
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432236
feature_type: variation
id: rs2145610670
seq_region_name: 17
source: dbSNP
start: 73432236
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432239
feature_type: variation
id: rs1599560488
seq_region_name: 17
source: dbSNP
start: 73432239
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1031692079
seq_region_name: 17
source: dbSNP
start: 73432241
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1755549705
seq_region_name: 17
source: dbSNP
start: 73432248
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1191789014
seq_region_name: 17
source: dbSNP
start: 73432253
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1468210424
seq_region_name: 17
source: dbSNP
start: 73432254
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432255
feature_type: variation
id: rs1253804408
seq_region_name: 17
source: dbSNP
start: 73432255
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432256
feature_type: variation
id: rs2063331621
seq_region_name: 17
source: dbSNP
start: 73432256
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432261
feature_type: variation
id: rs1224322618
seq_region_name: 17
source: dbSNP
start: 73432261
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73432262
feature_type: variation
id: rs567326532
seq_region_name: 17
source: dbSNP
start: 73432262
strand: 1
-
alleles:
- AAA
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432264
feature_type: variation
id: rs2063331668
seq_region_name: 17
source: dbSNP
start: 73432262
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432267
feature_type: variation
id: rs1740520635
seq_region_name: 17
source: dbSNP
start: 73432264
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432266
feature_type: variation
id: rs1272980480
seq_region_name: 17
source: dbSNP
start: 73432266
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432267
feature_type: variation
id: rs955718804
seq_region_name: 17
source: dbSNP
start: 73432267
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432271
feature_type: variation
id: rs2063331732
seq_region_name: 17
source: dbSNP
start: 73432267
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432268
feature_type: variation
id: rs1344885704
seq_region_name: 17
source: dbSNP
start: 73432268
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432271
feature_type: variation
id: rs1299181508
seq_region_name: 17
source: dbSNP
start: 73432271
strand: 1
-
alleles:
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- AGAGAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432283
feature_type: variation
id: rs2145610763
seq_region_name: 17
source: dbSNP
start: 73432276
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1231361647
seq_region_name: 17
source: dbSNP
start: 73432279
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1369861490
seq_region_name: 17
source: dbSNP
start: 73432285
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063331809
seq_region_name: 17
source: dbSNP
start: 73432286
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063331829
seq_region_name: 17
source: dbSNP
start: 73432289
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1293750124
seq_region_name: 17
source: dbSNP
start: 73432291
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063331883
seq_region_name: 17
source: dbSNP
start: 73432293
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432294
feature_type: variation
id: rs2063331900
seq_region_name: 17
source: dbSNP
start: 73432294
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145610808
seq_region_name: 17
source: dbSNP
start: 73432295
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1438396717
seq_region_name: 17
source: dbSNP
start: 73432301
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063331935
seq_region_name: 17
source: dbSNP
start: 73432302
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1474855537
seq_region_name: 17
source: dbSNP
start: 73432304
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063331983
seq_region_name: 17
source: dbSNP
start: 73432307
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332002
seq_region_name: 17
source: dbSNP
start: 73432310
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1352523600
seq_region_name: 17
source: dbSNP
start: 73432311
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332047
seq_region_name: 17
source: dbSNP
start: 73432313
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332070
seq_region_name: 17
source: dbSNP
start: 73432317
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332090
seq_region_name: 17
source: dbSNP
start: 73432318
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1327884244
seq_region_name: 17
source: dbSNP
start: 73432321
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432331
feature_type: variation
id: rs1430372200
seq_region_name: 17
source: dbSNP
start: 73432331
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs922610772
seq_region_name: 17
source: dbSNP
start: 73432334
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332186
seq_region_name: 17
source: dbSNP
start: 73432339
strand: 1
-
alleles:
- AA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332208
seq_region_name: 17
source: dbSNP
start: 73432348
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1395960579
seq_region_name: 17
source: dbSNP
start: 73432350
strand: 1
-
alleles:
- CCCCCC
- CCCCC
- CCCCCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs775987779
seq_region_name: 17
source: dbSNP
start: 73432350
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332262
seq_region_name: 17
source: dbSNP
start: 73432351
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1398511952
seq_region_name: 17
source: dbSNP
start: 73432352
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432353
feature_type: variation
id: rs930187902
seq_region_name: 17
source: dbSNP
start: 73432353
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1157730766
seq_region_name: 17
source: dbSNP
start: 73432355
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063332346
seq_region_name: 17
source: dbSNP
start: 73432357
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs983034318
seq_region_name: 17
source: dbSNP
start: 73432358
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432359
feature_type: variation
id: rs1359423041
seq_region_name: 17
source: dbSNP
start: 73432359
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs536447235
seq_region_name: 17
source: dbSNP
start: 73432361
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs914301832
seq_region_name: 17
source: dbSNP
start: 73432362
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432364
feature_type: variation
id: rs1437617255
seq_region_name: 17
source: dbSNP
start: 73432364
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs753147310
seq_region_name: 17
source: dbSNP
start: 73432367
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432371
feature_type: variation
id: rs2063332496
seq_region_name: 17
source: dbSNP
start: 73432371
strand: 1
-
alleles:
- A
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432374
feature_type: variation
id: rs1278796315
seq_region_name: 17
source: dbSNP
start: 73432374
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432377
feature_type: variation
id: rs1156987689
seq_region_name: 17
source: dbSNP
start: 73432377
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432378
feature_type: variation
id: rs2063332554
seq_region_name: 17
source: dbSNP
start: 73432378
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432379
feature_type: variation
id: rs2063332572
seq_region_name: 17
source: dbSNP
start: 73432379
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432380
feature_type: variation
id: rs1231531085
seq_region_name: 17
source: dbSNP
start: 73432380
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432384
feature_type: variation
id: rs947122979
seq_region_name: 17
source: dbSNP
start: 73432384
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432387
feature_type: variation
id: rs2145611026
seq_region_name: 17
source: dbSNP
start: 73432387
strand: 1
-
alleles:
- C
- CC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432390
feature_type: variation
id: rs2063332626
seq_region_name: 17
source: dbSNP
start: 73432390
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432393
feature_type: variation
id: rs1373955992
seq_region_name: 17
source: dbSNP
start: 73432393
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432394
feature_type: variation
id: rs2063332670
seq_region_name: 17
source: dbSNP
start: 73432394
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432398
feature_type: variation
id: rs974539201
seq_region_name: 17
source: dbSNP
start: 73432398
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432399
feature_type: variation
id: rs2063332709
seq_region_name: 17
source: dbSNP
start: 73432399
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432406
feature_type: variation
id: rs1220621389
seq_region_name: 17
source: dbSNP
start: 73432406
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432407
feature_type: variation
id: rs1037437660
seq_region_name: 17
source: dbSNP
start: 73432407
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432414
feature_type: variation
id: rs1278749361
seq_region_name: 17
source: dbSNP
start: 73432414
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432418
feature_type: variation
id: rs894918476
seq_region_name: 17
source: dbSNP
start: 73432418
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432419
feature_type: variation
id: rs577966696
seq_region_name: 17
source: dbSNP
start: 73432419
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432420
feature_type: variation
id: rs1222176377
seq_region_name: 17
source: dbSNP
start: 73432420
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432424
feature_type: variation
id: rs2145611127
seq_region_name: 17
source: dbSNP
start: 73432424
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432425
feature_type: variation
id: rs187380745
seq_region_name: 17
source: dbSNP
start: 73432425
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432426
feature_type: variation
id: rs1434235575
seq_region_name: 17
source: dbSNP
start: 73432426
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432428
feature_type: variation
id: rs2063332929
seq_region_name: 17
source: dbSNP
start: 73432428
strand: 1
-
alleles:
- ACTGAGTG
- ACTGAGTGACTGAGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432441
feature_type: variation
id: rs1359834884
seq_region_name: 17
source: dbSNP
start: 73432434
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432435
feature_type: variation
id: rs1178272467
seq_region_name: 17
source: dbSNP
start: 73432435
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432439
feature_type: variation
id: rs560363978
seq_region_name: 17
source: dbSNP
start: 73432439
strand: 1
-
alleles:
- TGGATGTGTTTATTTCCATG
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432468
feature_type: variation
id: rs950885107
seq_region_name: 17
source: dbSNP
start: 73432449
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432450
feature_type: variation
id: rs2063333014
seq_region_name: 17
source: dbSNP
start: 73432450
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432452
feature_type: variation
id: rs940678848
seq_region_name: 17
source: dbSNP
start: 73432452
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432454
feature_type: variation
id: rs534013340
seq_region_name: 17
source: dbSNP
start: 73432454
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432455
feature_type: variation
id: rs1256072921
seq_region_name: 17
source: dbSNP
start: 73432455
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432458
feature_type: variation
id: rs999366300
seq_region_name: 17
source: dbSNP
start: 73432458
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432465
feature_type: variation
id: rs2063333138
seq_region_name: 17
source: dbSNP
start: 73432465
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432466
feature_type: variation
id: rs2063333161
seq_region_name: 17
source: dbSNP
start: 73432466
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432470
feature_type: variation
id: rs899217189
seq_region_name: 17
source: dbSNP
start: 73432470
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432474
feature_type: variation
id: rs556127586
seq_region_name: 17
source: dbSNP
start: 73432474
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432477
feature_type: variation
id: rs2063333234
seq_region_name: 17
source: dbSNP
start: 73432477
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432478
feature_type: variation
id: rs1314782957
seq_region_name: 17
source: dbSNP
start: 73432478
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432486
feature_type: variation
id: rs1228854567
seq_region_name: 17
source: dbSNP
start: 73432486
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432488
feature_type: variation
id: rs2063333289
seq_region_name: 17
source: dbSNP
start: 73432488
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432489
feature_type: variation
id: rs560969373
seq_region_name: 17
source: dbSNP
start: 73432489
strand: 1
-
alleles:
- CCT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432495
feature_type: variation
id: rs1352069642
seq_region_name: 17
source: dbSNP
start: 73432493
strand: 1
-
alleles:
- T
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432495
feature_type: variation
id: rs1291154923
seq_region_name: 17
source: dbSNP
start: 73432495
strand: 1
-
alleles:
- A
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432496
feature_type: variation
id: rs146677356
seq_region_name: 17
source: dbSNP
start: 73432496
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432499
feature_type: variation
id: rs2063333399
seq_region_name: 17
source: dbSNP
start: 73432499
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432500
feature_type: variation
id: rs1234600067
seq_region_name: 17
source: dbSNP
start: 73432500
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432501
feature_type: variation
id: rs1011178742
seq_region_name: 17
source: dbSNP
start: 73432501
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432503
feature_type: variation
id: rs2063333429
seq_region_name: 17
source: dbSNP
start: 73432503
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432506
feature_type: variation
id: rs2145611306
seq_region_name: 17
source: dbSNP
start: 73432506
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432509
feature_type: variation
id: rs1468509378
seq_region_name: 17
source: dbSNP
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73432685
strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73432694
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73432702
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73432706
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73432713
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73432716
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432717
feature_type: variation
id: rs1393353292
seq_region_name: 17
source: dbSNP
start: 73432717
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432722
feature_type: variation
id: rs2145611851
seq_region_name: 17
source: dbSNP
start: 73432722
strand: 1
-
alleles:
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- CT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432725
feature_type: variation
id: rs2145611858
seq_region_name: 17
source: dbSNP
start: 73432722
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432724
feature_type: variation
id: rs2063335562
seq_region_name: 17
source: dbSNP
start: 73432724
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432726
feature_type: variation
id: rs200959640
seq_region_name: 17
source: dbSNP
start: 73432726
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432729
feature_type: variation
id: rs1461920770
seq_region_name: 17
source: dbSNP
start: 73432729
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432730
feature_type: variation
id: rs1046140437
seq_region_name: 17
source: dbSNP
start: 73432730
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432731
feature_type: variation
id: rs2063335719
seq_region_name: 17
source: dbSNP
start: 73432731
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432732
feature_type: variation
id: rs2063335754
seq_region_name: 17
source: dbSNP
start: 73432732
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432733
feature_type: variation
id: rs73347758
seq_region_name: 17
source: dbSNP
start: 73432733
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432735
feature_type: variation
id: rs2063335818
seq_region_name: 17
source: dbSNP
start: 73432735
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432738
feature_type: variation
id: rs2063335858
seq_region_name: 17
source: dbSNP
start: 73432738
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432740
feature_type: variation
id: rs754958164
seq_region_name: 17
source: dbSNP
start: 73432740
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432741
feature_type: variation
id: rs1052342555
seq_region_name: 17
source: dbSNP
start: 73432741
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432742
feature_type: variation
id: rs534054575
seq_region_name: 17
source: dbSNP
start: 73432742
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432744
feature_type: variation
id: rs1451771307
seq_region_name: 17
source: dbSNP
start: 73432744
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432745
feature_type: variation
id: rs1269240526
seq_region_name: 17
source: dbSNP
start: 73432745
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432746
feature_type: variation
id: rs1599560911
seq_region_name: 17
source: dbSNP
start: 73432746
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432752
feature_type: variation
id: rs1022584520
seq_region_name: 17
source: dbSNP
start: 73432752
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432753
feature_type: variation
id: rs2063336208
seq_region_name: 17
source: dbSNP
start: 73432753
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432756
feature_type: variation
id: rs2063336238
seq_region_name: 17
source: dbSNP
start: 73432756
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432757
feature_type: variation
id: rs1191199460
seq_region_name: 17
source: dbSNP
start: 73432757
strand: 1
-
alleles:
- TGTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432761
feature_type: variation
id: rs1567769250
seq_region_name: 17
source: dbSNP
start: 73432757
strand: 1
-
alleles:
- TGTTTGT
- TGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432765
feature_type: variation
id: rs553932055
seq_region_name: 17
source: dbSNP
start: 73432759
strand: 1
-
alleles:
- T
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432762
feature_type: variation
id: rs1010833913
seq_region_name: 17
source: dbSNP
start: 73432762
strand: 1
-
alleles:
- TGTACGTGTGTGTGCACATGTGTATGTAC
- TGTACGTGTGTGTGCACATGTGTATGTACGTGTGTGTGCACATGTGTATGTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432791
feature_type: variation
id: rs1449706311
seq_region_name: 17
source: dbSNP
start: 73432763
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432764
feature_type: variation
id: rs1599560928
seq_region_name: 17
source: dbSNP
start: 73432764
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432767
feature_type: variation
id: rs1345779749
seq_region_name: 17
source: dbSNP
start: 73432767
strand: 1
-
alleles:
- CG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432768
feature_type: variation
id: rs2063336425
seq_region_name: 17
source: dbSNP
start: 73432767
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432768
feature_type: variation
id: rs1039918662
seq_region_name: 17
source: dbSNP
start: 73432768
strand: 1
-
alleles:
- GTGTGTGTG
- GTGTGTG
- GTGTGTGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432776
feature_type: variation
id: rs66464388
seq_region_name: 17
source: dbSNP
start: 73432768
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432769
feature_type: variation
id: rs778648467
seq_region_name: 17
source: dbSNP
start: 73432769
strand: 1
-
alleles:
- TGTGTGTGCACATGTGTATGTACATGTGTGTGCA
- TGTGTGTGCA
- TGTGTGTGCACATGTGTATGTACATGTGTGTGCACATGTGTATGTACATGTGTGTGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432802
feature_type: variation
id: rs2063336603
seq_region_name: 17
source: dbSNP
start: 73432769
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432770
feature_type: variation
id: rs2063336639
seq_region_name: 17
source: dbSNP
start: 73432770
strand: 1
-
alleles:
- GTGTG
- GTGTGCACATGTGTTTGTACGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432774
feature_type: variation
id: rs2063336673
seq_region_name: 17
source: dbSNP
start: 73432770
strand: 1
-
alleles:
- TGTG
- TGTGCACATGTGTATGTACATGTGTGTGCATATGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432774
feature_type: variation
id: rs2063336709
seq_region_name: 17
source: dbSNP
start: 73432771
strand: 1
-
alleles:
- TGTGTGCACATGTGTATGTACATGTGTGTGCATATGTGTGCACATGTGTATGTAC
- TGTGTGCACATGTGTATGTAC
- TGTGTGCACATGTGTATGTACATGTGTGTGCATATGTGTGCACATGTGTATGTACATGTGTGTGCATATGTGTGCACATGTGTATGTAC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432825
feature_type: variation
id: rs1305322782
seq_region_name: 17
source: dbSNP
start: 73432771
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432772
feature_type: variation
id: rs2063336791
seq_region_name: 17
source: dbSNP
start: 73432772
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432773
feature_type: variation
id: rs1028723760
seq_region_name: 17
source: dbSNP
start: 73432773
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432775
feature_type: variation
id: rs899666797
seq_region_name: 17
source: dbSNP
start: 73432775
strand: 1
-
alleles:
- "-"
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432776
feature_type: variation
id: rs2063336894
seq_region_name: 17
source: dbSNP
start: 73432777
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432777
feature_type: variation
id: rs1310354082
seq_region_name: 17
source: dbSNP
start: 73432777
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432781
feature_type: variation
id: rs1431155940
seq_region_name: 17
source: dbSNP
start: 73432780
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432781
feature_type: variation
id: rs2063336960
seq_region_name: 17
source: dbSNP
start: 73432781
strand: 1
-
alleles:
- TGTGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432785
feature_type: variation
id: rs1373116424
seq_region_name: 17
source: dbSNP
start: 73432781
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432782
feature_type: variation
id: rs2063337023
seq_region_name: 17
source: dbSNP
start: 73432782
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432783
feature_type: variation
id: rs2063337037
seq_region_name: 17
source: dbSNP
start: 73432783
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432785
feature_type: variation
id: rs2063337058
seq_region_name: 17
source: dbSNP
start: 73432785
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432786
feature_type: variation
id: rs2063337079
seq_region_name: 17
source: dbSNP
start: 73432786
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432787
feature_type: variation
id: rs1171442833
seq_region_name: 17
source: dbSNP
start: 73432787
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432789
feature_type: variation
id: rs1599560987
seq_region_name: 17
source: dbSNP
start: 73432789
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432790
feature_type: variation
id: rs2063337120
seq_region_name: 17
source: dbSNP
start: 73432790
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432791
feature_type: variation
id: rs1478155719
seq_region_name: 17
source: dbSNP
start: 73432791
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432792
feature_type: variation
id: rs998235775
seq_region_name: 17
source: dbSNP
start: 73432792
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432793
feature_type: variation
id: rs1422040477
seq_region_name: 17
source: dbSNP
start: 73432792
strand: 1
-
alleles:
- ATGT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432795
feature_type: variation
id: rs1834993235
seq_region_name: 17
source: dbSNP
start: 73432792
strand: 1
-
alleles:
- "-"
- CG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432792
feature_type: variation
id: rs2063337201
seq_region_name: 17
source: dbSNP
start: 73432793
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432793
feature_type: variation
id: rs117043974
seq_region_name: 17
source: dbSNP
start: 73432793
strand: 1
-
alleles:
- TGTGTGTG
- TGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432800
feature_type: variation
id: rs1472141349
seq_region_name: 17
source: dbSNP
start: 73432793
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432794
feature_type: variation
id: rs2063337251
seq_region_name: 17
source: dbSNP
start: 73432794
strand: 1
-
alleles:
- GTGTG
- GTGTGCATATGTGTGCACATGTGTATGTACACGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432798
feature_type: variation
id: rs2063337273
seq_region_name: 17
source: dbSNP
start: 73432794
strand: 1
-
alleles:
- TGTGTGCATATGTGTGCA
- TGTGTGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432812
feature_type: variation
id: rs1445026811
seq_region_name: 17
source: dbSNP
start: 73432795
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432796
feature_type: variation
id: rs2063337324
seq_region_name: 17
source: dbSNP
start: 73432796
strand: 1
-
alleles:
- GTGTGCATATGTGTGCACATGTGTATGTACGTGTGCAT
- GTGTGCATATGTGTGCACATGTGTATGTACGTGTGCATATGTGTGCACATGTGTATGTACGTGTGCAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432833
feature_type: variation
id: rs2063337348
seq_region_name: 17
source: dbSNP
start: 73432796
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432799
feature_type: variation
id: rs951343483
seq_region_name: 17
source: dbSNP
start: 73432799
strand: 1
-
alleles:
- ATAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432805
feature_type: variation
id: rs139667695
seq_region_name: 17
source: dbSNP
start: 73432802
strand: 1
-
alleles:
- T
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432803
feature_type: variation
id: rs192883805
seq_region_name: 17
source: dbSNP
start: 73432803
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432804
feature_type: variation
id: rs1599561027
seq_region_name: 17
source: dbSNP
start: 73432804
strand: 1
-
alleles:
- ATGTGTGCACATGTGT
- ATGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432819
feature_type: variation
id: rs2063337472
seq_region_name: 17
source: dbSNP
start: 73432804
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432805
feature_type: variation
id: rs2063337489
seq_region_name: 17
source: dbSNP
start: 73432805
strand: 1
-
alleles:
- TGTGT
- TGTGTATGTACACGTGTGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432809
feature_type: variation
id: rs1567769307
seq_region_name: 17
source: dbSNP
start: 73432805
strand: 1
-
alleles:
- TGTGTG
- TGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432810
feature_type: variation
id: rs2063337530
seq_region_name: 17
source: dbSNP
start: 73432805
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432806
feature_type: variation
id: rs1347469720
seq_region_name: 17
source: dbSNP
start: 73432806
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432808
feature_type: variation
id: rs1259179611
seq_region_name: 17
source: dbSNP
start: 73432808
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432809
feature_type: variation
id: rs2063337582
seq_region_name: 17
source: dbSNP
start: 73432809
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432810
feature_type: variation
id: rs2063337602
seq_region_name: 17
source: dbSNP
start: 73432810
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432812
feature_type: variation
id: rs567690293
seq_region_name: 17
source: dbSNP
start: 73432812
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432813
feature_type: variation
id: rs2063337635
seq_region_name: 17
source: dbSNP
start: 73432813
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432814
feature_type: variation
id: rs1351464157
seq_region_name: 17
source: dbSNP
start: 73432814
strand: 1
-
alleles:
- AT
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432815
feature_type: variation
id: rs1395844858
seq_region_name: 17
source: dbSNP
start: 73432814
strand: 1
-
alleles:
- T
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432815
feature_type: variation
id: rs1290543018
seq_region_name: 17
source: dbSNP
start: 73432815
strand: 1
-
alleles:
- TGTGT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432819
feature_type: variation
id: rs2063337704
seq_region_name: 17
source: dbSNP
start: 73432815
strand: 1
-
alleles:
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- TGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432844
feature_type: variation
id: rs2063337728
seq_region_name: 17
source: dbSNP
start: 73432815
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063337747
seq_region_name: 17
source: dbSNP
start: 73432816
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063337765
seq_region_name: 17
source: dbSNP
start: 73432817
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1443288071
seq_region_name: 17
source: dbSNP
start: 73432818
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1355308223
seq_region_name: 17
source: dbSNP
start: 73432819
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432821
feature_type: variation
id: rs2145612387
seq_region_name: 17
source: dbSNP
start: 73432821
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1414532020
seq_region_name: 17
source: dbSNP
start: 73432822
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432823
feature_type: variation
id: rs2063337827
seq_region_name: 17
source: dbSNP
start: 73432823
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432824
feature_type: variation
id: rs1599561076
seq_region_name: 17
source: dbSNP
start: 73432824
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432825
feature_type: variation
id: rs537859076
seq_region_name: 17
source: dbSNP
start: 73432825
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432826
feature_type: variation
id: rs539287126
seq_region_name: 17
source: dbSNP
start: 73432826
strand: 1
-
alleles:
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- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432835
feature_type: variation
id: rs1156419844
seq_region_name: 17
source: dbSNP
start: 73432826
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432842
feature_type: variation
id: rs1599561090
seq_region_name: 17
source: dbSNP
start: 73432826
strand: 1
-
alleles:
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- GTGTGCATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1456556493
seq_region_name: 17
source: dbSNP
start: 73432826
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432827
feature_type: variation
id: rs143512878
seq_region_name: 17
source: dbSNP
start: 73432827
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs973712390
seq_region_name: 17
source: dbSNP
start: 73432829
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432831
feature_type: variation
id: rs370156552
seq_region_name: 17
source: dbSNP
start: 73432831
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs373528186
seq_region_name: 17
source: dbSNP
start: 73432832
strand: 1
-
alleles:
- ATGTATGT
- ATGT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs375895640
seq_region_name: 17
source: dbSNP
start: 73432832
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1208369513
seq_region_name: 17
source: dbSNP
start: 73432833
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432835
feature_type: variation
id: rs2145612500
seq_region_name: 17
source: dbSNP
start: 73432833
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs948026863
seq_region_name: 17
source: dbSNP
start: 73432834
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs746460665
seq_region_name: 17
source: dbSNP
start: 73432835
strand: 1
-
alleles:
- TAT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432837
feature_type: variation
id: rs1045061682
seq_region_name: 17
source: dbSNP
start: 73432835
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432836
feature_type: variation
id: rs1285300836
seq_region_name: 17
source: dbSNP
start: 73432836
strand: 1
-
alleles:
- ATGTGTGTGCATGTGTGTGCA
- ATGTGTGTGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432856
feature_type: variation
id: rs1337126811
seq_region_name: 17
source: dbSNP
start: 73432836
strand: 1
-
alleles:
- TGTGTGTG
- TGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432844
feature_type: variation
id: rs939440190
seq_region_name: 17
source: dbSNP
start: 73432837
strand: 1
-
alleles:
- TGTGTGTGCATGTGTGTGCACATGCGTGTGTGTGCAT
- TGTGTGTGCAT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432873
feature_type: variation
id: rs1341723473
seq_region_name: 17
source: dbSNP
start: 73432837
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432838
feature_type: variation
id: rs1599561161
seq_region_name: 17
source: dbSNP
start: 73432838
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432839
feature_type: variation
id: rs2063338328
seq_region_name: 17
source: dbSNP
start: 73432839
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432841
feature_type: variation
id: rs150950054
seq_region_name: 17
source: dbSNP
start: 73432841
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432843
feature_type: variation
id: rs770495659
seq_region_name: 17
source: dbSNP
start: 73432843
strand: 1
-
alleles:
- TGCATGTGTGTGCACATGC
- TGC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063338393
seq_region_name: 17
source: dbSNP
start: 73432843
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432844
feature_type: variation
id: rs1213759294
seq_region_name: 17
source: dbSNP
start: 73432844
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432846
feature_type: variation
id: rs1433905307
seq_region_name: 17
source: dbSNP
start: 73432846
strand: 1
-
alleles:
- AT
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432847
feature_type: variation
id: rs1315554048
seq_region_name: 17
source: dbSNP
start: 73432846
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432847
feature_type: variation
id: rs776326172
seq_region_name: 17
source: dbSNP
start: 73432847
strand: 1
-
alleles:
- TGTGTGTG
- TGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432854
feature_type: variation
id: rs577653025
seq_region_name: 17
source: dbSNP
start: 73432847
strand: 1
-
alleles:
- TGTGTGTGCACATGCGTGTGTGTGCA
- TGTGTGTGCA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432872
feature_type: variation
id: rs1161172533
seq_region_name: 17
source: dbSNP
start: 73432847
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432848
feature_type: variation
id: rs1413029525
seq_region_name: 17
source: dbSNP
start: 73432848
strand: 1
-
alleles:
- T
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432851
feature_type: variation
id: rs892624132
seq_region_name: 17
source: dbSNP
start: 73432851
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432853
feature_type: variation
id: rs2063338570
seq_region_name: 17
source: dbSNP
start: 73432853
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432854
feature_type: variation
id: rs1163747902
seq_region_name: 17
source: dbSNP
start: 73432854
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432855
feature_type: variation
id: rs1851434070
seq_region_name: 17
source: dbSNP
start: 73432855
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432856
feature_type: variation
id: rs2063338601
seq_region_name: 17
source: dbSNP
start: 73432856
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432857
feature_type: variation
id: rs2063338623
seq_region_name: 17
source: dbSNP
start: 73432857
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432860
feature_type: variation
id: rs373862082
seq_region_name: 17
source: dbSNP
start: 73432860
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432861
feature_type: variation
id: rs377489131
seq_region_name: 17
source: dbSNP
start: 73432861
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432862
feature_type: variation
id: rs1211330938
seq_region_name: 17
source: dbSNP
start: 73432862
strand: 1
-
alleles:
- GTGTGTGTG
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432870
feature_type: variation
id: rs781747018
seq_region_name: 17
source: dbSNP
start: 73432862
strand: 1
-
alleles:
- TGTGTGTGCATATGTGTGTG
- TGTGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432882
feature_type: variation
id: rs1250121821
seq_region_name: 17
source: dbSNP
start: 73432863
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432869
feature_type: variation
id: rs2063338776
seq_region_name: 17
source: dbSNP
start: 73432869
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432870
feature_type: variation
id: rs1212285572
seq_region_name: 17
source: dbSNP
start: 73432870
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432872
feature_type: variation
id: rs1599561235
seq_region_name: 17
source: dbSNP
start: 73432872
strand: 1
-
alleles:
- ATAT
- AT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432875
feature_type: variation
id: rs900105122
seq_region_name: 17
source: dbSNP
start: 73432872
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432873
feature_type: variation
id: rs1291288268
seq_region_name: 17
source: dbSNP
start: 73432873
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432874
feature_type: variation
id: rs1465090564
seq_region_name: 17
source: dbSNP
start: 73432874
strand: 1
-
alleles:
- TGTGTGTGTGTG
- TGTGTGTG
- TGTGTGTGTG
- TGTGTGTGTGTGTG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432886
feature_type: variation
id: rs995803749
seq_region_name: 17
source: dbSNP
start: 73432875
strand: 1
-
alleles:
- T
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432877
feature_type: variation
id: rs1599561253
seq_region_name: 17
source: dbSNP
start: 73432877
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432880
feature_type: variation
id: rs2063338935
seq_region_name: 17
source: dbSNP
start: 73432880
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432881
feature_type: variation
id: rs1227004335
seq_region_name: 17
source: dbSNP
start: 73432881
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432886
feature_type: variation
id: rs2063338974
seq_region_name: 17
source: dbSNP
start: 73432886
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432890
feature_type: variation
id: rs2063338995
seq_region_name: 17
source: dbSNP
start: 73432890
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432892
feature_type: variation
id: rs1599561257
seq_region_name: 17
source: dbSNP
start: 73432892
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432895
feature_type: variation
id: rs2063339012
seq_region_name: 17
source: dbSNP
start: 73432895
strand: 1
-
alleles:
- AG
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432904
feature_type: variation
id: rs1365555499
seq_region_name: 17
source: dbSNP
start: 73432903
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432904
feature_type: variation
id: rs2063339054
seq_region_name: 17
source: dbSNP
start: 73432904
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432906
feature_type: variation
id: rs1028671588
seq_region_name: 17
source: dbSNP
start: 73432906
strand: 1
-
alleles:
- G
- GCACACACAG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432907
feature_type: variation
id: rs2063339090
seq_region_name: 17
source: dbSNP
start: 73432907
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432912
feature_type: variation
id: rs2063339109
seq_region_name: 17
source: dbSNP
start: 73432912
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432913
feature_type: variation
id: rs1434090210
seq_region_name: 17
source: dbSNP
start: 73432913
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432914
feature_type: variation
id: rs927739348
seq_region_name: 17
source: dbSNP
start: 73432914
strand: 1
-
alleles:
- CACACACA
- CACACA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432921
feature_type: variation
id: rs1349111036
seq_region_name: 17
source: dbSNP
start: 73432914
strand: 1
-
alleles:
- ACAGA
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432923
feature_type: variation
id: rs2145612835
seq_region_name: 17
source: dbSNP
start: 73432919
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432920
feature_type: variation
id: rs1599561271
seq_region_name: 17
source: dbSNP
start: 73432920
strand: 1
-
alleles:
- AGAG
- AG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432924
feature_type: variation
id: rs1407019300
seq_region_name: 17
source: dbSNP
start: 73432921
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432922
feature_type: variation
id: rs572249892
seq_region_name: 17
source: dbSNP
start: 73432922
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432924
feature_type: variation
id: rs1168105723
seq_region_name: 17
source: dbSNP
start: 73432924
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432925
feature_type: variation
id: rs1450164894
seq_region_name: 17
source: dbSNP
start: 73432925
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432930
feature_type: variation
id: rs934982808
seq_region_name: 17
source: dbSNP
start: 73432930
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432933
feature_type: variation
id: rs2063339368
seq_region_name: 17
source: dbSNP
start: 73432933
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432935
feature_type: variation
id: rs1191963804
seq_region_name: 17
source: dbSNP
start: 73432935
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73432936
feature_type: variation
id: rs2063339414
seq_region_name: 17
source: dbSNP
start: 73432936
strand: 1
-
alleles:
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- T
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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alleles:
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73433060
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73433070
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433072
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433074
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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start: 73433074
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73433076
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73433077
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73433078
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433080
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73433083
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433084
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73433085
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433087
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433088
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433089
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs1360005367
seq_region_name: 17
source: dbSNP
start: 73433092
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433095
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433097
strand: 1
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alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433108
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433109
strand: 1
-
alleles:
- "-"
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433115
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433120
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433125
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1473865743
seq_region_name: 17
source: dbSNP
start: 73433125
strand: 1
-
alleles:
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- TCTCTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs141946835
seq_region_name: 17
source: dbSNP
start: 73433128
strand: 1
-
alleles:
- TCTAGTCT
- TCTAGTCTCTAGTCT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433135
feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433128
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433130
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433133
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433148
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433149
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs900051335
seq_region_name: 17
source: dbSNP
start: 73433150
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063340966
seq_region_name: 17
source: dbSNP
start: 73433151
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433154
feature_type: variation
id: rs2063340988
seq_region_name: 17
source: dbSNP
start: 73433154
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433156
feature_type: variation
id: rs2063341012
seq_region_name: 17
source: dbSNP
start: 73433156
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433160
feature_type: variation
id: rs1267266462
seq_region_name: 17
source: dbSNP
start: 73433160
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1228723453
seq_region_name: 17
source: dbSNP
start: 73433162
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063341071
seq_region_name: 17
source: dbSNP
start: 73433166
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs574882275
seq_region_name: 17
source: dbSNP
start: 73433167
strand: 1
-
alleles:
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- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs914858148
seq_region_name: 17
source: dbSNP
start: 73433177
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs543889419
seq_region_name: 17
source: dbSNP
start: 73433180
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1395571922
seq_region_name: 17
source: dbSNP
start: 73433184
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063341156
seq_region_name: 17
source: dbSNP
start: 73433185
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433187
feature_type: variation
id: rs1313291617
seq_region_name: 17
source: dbSNP
start: 73433187
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433188
feature_type: variation
id: rs1237506594
seq_region_name: 17
source: dbSNP
start: 73433188
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433189
feature_type: variation
id: rs2063341224
seq_region_name: 17
source: dbSNP
start: 73433188
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433203
feature_type: variation
id: rs1304617821
seq_region_name: 17
source: dbSNP
start: 73433203
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433210
feature_type: variation
id: rs2145613516
seq_region_name: 17
source: dbSNP
start: 73433204
strand: 1
-
alleles:
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433205
feature_type: variation
id: rs2049473170
seq_region_name: 17
source: dbSNP
start: 73433205
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063341243
seq_region_name: 17
source: dbSNP
start: 73433209
strand: 1
-
alleles:
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433218
feature_type: variation
id: rs2063341260
seq_region_name: 17
source: dbSNP
start: 73433218
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433220
feature_type: variation
id: rs2145613541
seq_region_name: 17
source: dbSNP
start: 73433220
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433221
feature_type: variation
id: rs1376975475
seq_region_name: 17
source: dbSNP
start: 73433221
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433222
feature_type: variation
id: rs12601153
seq_region_name: 17
source: dbSNP
start: 73433222
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1388106742
seq_region_name: 17
source: dbSNP
start: 73433226
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433228
feature_type: variation
id: rs1292655046
seq_region_name: 17
source: dbSNP
start: 73433228
strand: 1
-
alleles:
- G
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433229
feature_type: variation
id: rs1321711980
seq_region_name: 17
source: dbSNP
start: 73433229
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433231
feature_type: variation
id: rs2063341405
seq_region_name: 17
source: dbSNP
start: 73433231
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433235
feature_type: variation
id: rs2063341422
seq_region_name: 17
source: dbSNP
start: 73433235
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433236
feature_type: variation
id: rs1336277724
seq_region_name: 17
source: dbSNP
start: 73433236
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433247
feature_type: variation
id: rs1240616113
seq_region_name: 17
source: dbSNP
start: 73433247
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433248
feature_type: variation
id: rs890100685
seq_region_name: 17
source: dbSNP
start: 73433248
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433249
feature_type: variation
id: rs975732508
seq_region_name: 17
source: dbSNP
start: 73433249
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433250
feature_type: variation
id: rs921211721
seq_region_name: 17
source: dbSNP
start: 73433250
strand: 1
-
alleles:
- A
- AA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433251
feature_type: variation
id: rs1349536352
seq_region_name: 17
source: dbSNP
start: 73433251
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433252
feature_type: variation
id: rs2063341547
seq_region_name: 17
source: dbSNP
start: 73433252
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433253
feature_type: variation
id: rs117730567
seq_region_name: 17
source: dbSNP
start: 73433253
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433255
feature_type: variation
id: rs2145613648
seq_region_name: 17
source: dbSNP
start: 73433255
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433258
feature_type: variation
id: rs1239418895
seq_region_name: 17
source: dbSNP
start: 73433258
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433262
feature_type: variation
id: rs2040043807
seq_region_name: 17
source: dbSNP
start: 73433262
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433263
feature_type: variation
id: rs549925779
seq_region_name: 17
source: dbSNP
start: 73433263
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433268
feature_type: variation
id: rs2063341632
seq_region_name: 17
source: dbSNP
start: 73433268
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433270
feature_type: variation
id: rs2063341649
seq_region_name: 17
source: dbSNP
start: 73433270
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433274
feature_type: variation
id: rs1599561599
seq_region_name: 17
source: dbSNP
start: 73433274
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433275
feature_type: variation
id: rs1281502049
seq_region_name: 17
source: dbSNP
start: 73433275
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433280
feature_type: variation
id: rs2063341710
seq_region_name: 17
source: dbSNP
start: 73433280
strand: 1
-
alleles:
- G
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- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433281
feature_type: variation
id: rs1050893095
seq_region_name: 17
source: dbSNP
start: 73433281
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433284
feature_type: variation
id: rs897590879
seq_region_name: 17
source: dbSNP
start: 73433284
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433286
feature_type: variation
id: rs994587925
seq_region_name: 17
source: dbSNP
start: 73433286
strand: 1
-
alleles:
- TCTTT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433291
feature_type: variation
id: rs1209171444
seq_region_name: 17
source: dbSNP
start: 73433287
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433288
feature_type: variation
id: rs76837067
seq_region_name: 17
source: dbSNP
start: 73433288
strand: 1
-
alleles:
- C
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433288
feature_type: variation
id: rs2063341873
seq_region_name: 17
source: dbSNP
start: 73433288
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433289
feature_type: variation
id: rs1599561627
seq_region_name: 17
source: dbSNP
start: 73433289
strand: 1
-
alleles:
- TTTTTTTTTTTT
- TTTTTTTTTT
- TTTTTTTTTTT
- TTTTTTTTTTTTT
- TTTTTTTTTTTTTT
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433300
feature_type: variation
id: rs71157015
seq_region_name: 17
source: dbSNP
start: 73433289
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433290
feature_type: variation
id: rs1263402301
seq_region_name: 17
source: dbSNP
start: 73433290
strand: 1
-
alleles:
- "-"
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433290
feature_type: variation
id: rs2063341994
seq_region_name: 17
source: dbSNP
start: 73433291
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433294
feature_type: variation
id: rs1567769702
seq_region_name: 17
source: dbSNP
start: 73433294
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433300
feature_type: variation
id: rs2063342038
seq_region_name: 17
source: dbSNP
start: 73433300
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433301
feature_type: variation
id: rs2063342056
seq_region_name: 17
source: dbSNP
start: 73433301
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433304
feature_type: variation
id: rs969227619
seq_region_name: 17
source: dbSNP
start: 73433304
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433305
feature_type: variation
id: rs1257479969
seq_region_name: 17
source: dbSNP
start: 73433305
strand: 1
-
alleles:
- G
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433306
feature_type: variation
id: rs138646968
seq_region_name: 17
source: dbSNP
start: 73433306
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433311
feature_type: variation
id: rs2063342143
seq_region_name: 17
source: dbSNP
start: 73433311
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433313
feature_type: variation
id: rs1364822410
seq_region_name: 17
source: dbSNP
start: 73433313
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433314
feature_type: variation
id: rs1034922942
seq_region_name: 17
source: dbSNP
start: 73433314
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433317
feature_type: variation
id: rs2063342187
seq_region_name: 17
source: dbSNP
start: 73433317
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433319
feature_type: variation
id: rs2063342207
seq_region_name: 17
source: dbSNP
start: 73433319
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433323
feature_type: variation
id: rs1828337761
seq_region_name: 17
source: dbSNP
start: 73433323
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433324
feature_type: variation
id: rs2063342228
seq_region_name: 17
source: dbSNP
start: 73433324
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433326
feature_type: variation
id: rs773181334
seq_region_name: 17
source: dbSNP
start: 73433326
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433329
feature_type: variation
id: rs886944640
seq_region_name: 17
source: dbSNP
start: 73433329
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433331
feature_type: variation
id: rs2063342296
seq_region_name: 17
source: dbSNP
start: 73433331
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433334
feature_type: variation
id: rs1293264837
seq_region_name: 17
source: dbSNP
start: 73433334
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433335
feature_type: variation
id: rs1599561685
seq_region_name: 17
source: dbSNP
start: 73433335
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433339
feature_type: variation
id: rs1944505382
seq_region_name: 17
source: dbSNP
start: 73433339
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433345
feature_type: variation
id: rs1362091081
seq_region_name: 17
source: dbSNP
start: 73433345
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433346
feature_type: variation
id: rs1599561701
seq_region_name: 17
source: dbSNP
start: 73433346
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433347
feature_type: variation
id: rs2063342378
seq_region_name: 17
source: dbSNP
start: 73433347
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433349
feature_type: variation
id: rs1567769734
seq_region_name: 17
source: dbSNP
start: 73433349
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433351
feature_type: variation
id: rs2063342415
seq_region_name: 17
source: dbSNP
start: 73433351
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433352
feature_type: variation
id: rs2145613938
seq_region_name: 17
source: dbSNP
start: 73433352
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433353
feature_type: variation
id: rs2063342433
seq_region_name: 17
source: dbSNP
start: 73433353
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433358
feature_type: variation
id: rs1458873882
seq_region_name: 17
source: dbSNP
start: 73433358
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433362
feature_type: variation
id: rs2063342477
seq_region_name: 17
source: dbSNP
start: 73433362
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433364
feature_type: variation
id: rs1599561706
seq_region_name: 17
source: dbSNP
start: 73433364
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433365
feature_type: variation
id: rs1352069936
seq_region_name: 17
source: dbSNP
start: 73433365
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433367
feature_type: variation
id: rs2063342536
seq_region_name: 17
source: dbSNP
start: 73433367
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433371
feature_type: variation
id: rs2063342549
seq_region_name: 17
source: dbSNP
start: 73433371
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433374
feature_type: variation
id: rs1415719875
seq_region_name: 17
source: dbSNP
start: 73433374
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433376
feature_type: variation
id: rs1447094600
seq_region_name: 17
source: dbSNP
start: 73433376
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433377
feature_type: variation
id: rs2063342613
seq_region_name: 17
source: dbSNP
start: 73433377
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
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alleles:
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alleles:
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-
alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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strand: 1
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alleles:
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assembly_name: GRCh38
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs2063342989
seq_region_name: 17
source: dbSNP
start: 73433445
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433447
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433453
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73433456
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1393019103
seq_region_name: 17
source: dbSNP
start: 73433459
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433461
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73433468
strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
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start: 73433474
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
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start: 73433475
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
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strand: 1
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alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73433477
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433478
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433479
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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seq_region_name: 17
source: dbSNP
start: 73433484
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1022082595
seq_region_name: 17
source: dbSNP
start: 73433488
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433490
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs1343215112
seq_region_name: 17
source: dbSNP
start: 73433493
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433495
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73433496
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2145614293
seq_region_name: 17
source: dbSNP
start: 73433508
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063343478
seq_region_name: 17
source: dbSNP
start: 73433510
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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end: 73433514
feature_type: variation
id: rs2063343502
seq_region_name: 17
source: dbSNP
start: 73433514
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433521
feature_type: variation
id: rs552924164
seq_region_name: 17
source: dbSNP
start: 73433521
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433524
feature_type: variation
id: rs968099618
seq_region_name: 17
source: dbSNP
start: 73433524
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063343536
seq_region_name: 17
source: dbSNP
start: 73433528
strand: 1
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alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs975078529
seq_region_name: 17
source: dbSNP
start: 73433532
strand: 1
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alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1314326936
seq_region_name: 17
source: dbSNP
start: 73433534
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433535
feature_type: variation
id: rs11652365
seq_region_name: 17
source: dbSNP
start: 73433535
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433546
feature_type: variation
id: rs2063343593
seq_region_name: 17
source: dbSNP
start: 73433536
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433542
feature_type: variation
id: rs751754088
seq_region_name: 17
source: dbSNP
start: 73433542
strand: 1
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alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433545
feature_type: variation
id: rs1248521507
seq_region_name: 17
source: dbSNP
start: 73433545
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433547
feature_type: variation
id: rs1351591357
seq_region_name: 17
source: dbSNP
start: 73433547
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433550
feature_type: variation
id: rs1437372031
seq_region_name: 17
source: dbSNP
start: 73433550
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433552
feature_type: variation
id: rs2063343684
seq_region_name: 17
source: dbSNP
start: 73433552
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433553
feature_type: variation
id: rs944345648
seq_region_name: 17
source: dbSNP
start: 73433553
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433554
feature_type: variation
id: rs933857334
seq_region_name: 17
source: dbSNP
start: 73433554
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433555
feature_type: variation
id: rs1171626263
seq_region_name: 17
source: dbSNP
start: 73433555
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433558
feature_type: variation
id: rs986723368
seq_region_name: 17
source: dbSNP
start: 73433558
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433564
feature_type: variation
id: rs1431162129
seq_region_name: 17
source: dbSNP
start: 73433564
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433569
feature_type: variation
id: rs527291509
seq_region_name: 17
source: dbSNP
start: 73433569
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433571
feature_type: variation
id: rs1472235452
seq_region_name: 17
source: dbSNP
start: 73433571
strand: 1
-
alleles:
- G
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433571
feature_type: variation
id: rs2145614454
seq_region_name: 17
source: dbSNP
start: 73433571
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433575
feature_type: variation
id: rs2063343832
seq_region_name: 17
source: dbSNP
start: 73433575
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433578
feature_type: variation
id: rs939910042
seq_region_name: 17
source: dbSNP
start: 73433578
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433579
feature_type: variation
id: rs543487930
seq_region_name: 17
source: dbSNP
start: 73433579
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433580
feature_type: variation
id: rs1440762634
seq_region_name: 17
source: dbSNP
start: 73433580
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433581
feature_type: variation
id: rs898606989
seq_region_name: 17
source: dbSNP
start: 73433581
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433584
feature_type: variation
id: rs1201255301
seq_region_name: 17
source: dbSNP
start: 73433584
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433585
feature_type: variation
id: rs948827313
seq_region_name: 17
source: dbSNP
start: 73433585
strand: 1
-
alleles:
- C
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- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433588
feature_type: variation
id: rs1044349265
seq_region_name: 17
source: dbSNP
start: 73433588
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433589
feature_type: variation
id: rs907212920
seq_region_name: 17
source: dbSNP
start: 73433589
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433592
feature_type: variation
id: rs960659695
seq_region_name: 17
source: dbSNP
start: 73433592
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433596
feature_type: variation
id: rs117482004
seq_region_name: 17
source: dbSNP
start: 73433596
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433597
feature_type: variation
id: rs2063344043
seq_region_name: 17
source: dbSNP
start: 73433597
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433598
feature_type: variation
id: rs2063344065
seq_region_name: 17
source: dbSNP
start: 73433598
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433599
feature_type: variation
id: rs74766034
seq_region_name: 17
source: dbSNP
start: 73433599
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433601
feature_type: variation
id: rs1338206023
seq_region_name: 17
source: dbSNP
start: 73433601
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433605
feature_type: variation
id: rs2063344149
seq_region_name: 17
source: dbSNP
start: 73433605
strand: 1
-
alleles:
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- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433606
feature_type: variation
id: rs891955707
seq_region_name: 17
source: dbSNP
start: 73433606
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1011770165
seq_region_name: 17
source: dbSNP
start: 73433607
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433627
feature_type: variation
id: rs1599561957
seq_region_name: 17
source: dbSNP
start: 73433627
strand: 1
-
alleles:
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- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433629
feature_type: variation
id: rs2063344228
seq_region_name: 17
source: dbSNP
start: 73433629
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433631
feature_type: variation
id: rs1022224995
seq_region_name: 17
source: dbSNP
start: 73433631
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433636
feature_type: variation
id: rs2063344271
seq_region_name: 17
source: dbSNP
start: 73433636
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433637
feature_type: variation
id: rs8071524
seq_region_name: 17
source: dbSNP
start: 73433637
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433638
feature_type: variation
id: rs560420810
seq_region_name: 17
source: dbSNP
start: 73433638
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433639
feature_type: variation
id: rs1456477939
seq_region_name: 17
source: dbSNP
start: 73433639
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433641
feature_type: variation
id: rs1412697068
seq_region_name: 17
source: dbSNP
start: 73433641
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433642
feature_type: variation
id: rs921381142
seq_region_name: 17
source: dbSNP
start: 73433642
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433648
feature_type: variation
id: rs2063344420
seq_region_name: 17
source: dbSNP
start: 73433648
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433649
feature_type: variation
id: rs2063344445
seq_region_name: 17
source: dbSNP
start: 73433649
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433650
feature_type: variation
id: rs954167341
seq_region_name: 17
source: dbSNP
start: 73433650
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433653
feature_type: variation
id: rs1368002710
seq_region_name: 17
source: dbSNP
start: 73433653
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433658
feature_type: variation
id: rs1599561989
seq_region_name: 17
source: dbSNP
start: 73433658
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433661
feature_type: variation
id: rs1027958322
seq_region_name: 17
source: dbSNP
start: 73433661
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433662
feature_type: variation
id: rs955061489
seq_region_name: 17
source: dbSNP
start: 73433662
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433664
feature_type: variation
id: rs2063344561
seq_region_name: 17
source: dbSNP
start: 73433664
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433666
feature_type: variation
id: rs986716461
seq_region_name: 17
source: dbSNP
start: 73433666
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433667
feature_type: variation
id: rs1439654805
seq_region_name: 17
source: dbSNP
start: 73433667
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433670
feature_type: variation
id: rs185517257
seq_region_name: 17
source: dbSNP
start: 73433670
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433674
feature_type: variation
id: rs2063344655
seq_region_name: 17
source: dbSNP
start: 73433674
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433675
feature_type: variation
id: rs908484434
seq_region_name: 17
source: dbSNP
start: 73433675
strand: 1
-
alleles:
- A
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433680
feature_type: variation
id: rs542871506
seq_region_name: 17
source: dbSNP
start: 73433680
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433681
feature_type: variation
id: rs2145614735
seq_region_name: 17
source: dbSNP
start: 73433681
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433683
feature_type: variation
id: rs1208568236
seq_region_name: 17
source: dbSNP
start: 73433683
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433686
feature_type: variation
id: rs1270670526
seq_region_name: 17
source: dbSNP
start: 73433686
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433687
feature_type: variation
id: rs752499468
seq_region_name: 17
source: dbSNP
start: 73433687
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433690
feature_type: variation
id: rs758241886
seq_region_name: 17
source: dbSNP
start: 73433690
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433691
feature_type: variation
id: rs760370351
seq_region_name: 17
source: dbSNP
start: 73433691
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433693
feature_type: variation
id: rs1239293561
seq_region_name: 17
source: dbSNP
start: 73433693
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433696
feature_type: variation
id: rs1599562035
seq_region_name: 17
source: dbSNP
start: 73433696
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433697
feature_type: variation
id: rs1286712234
seq_region_name: 17
source: dbSNP
start: 73433697
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433698
feature_type: variation
id: rs199937330
seq_region_name: 17
source: dbSNP
start: 73433698
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433699
feature_type: variation
id: rs912764665
seq_region_name: 17
source: dbSNP
start: 73433699
strand: 1
-
alleles:
- C
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433702
feature_type: variation
id: rs1175840671
seq_region_name: 17
source: dbSNP
start: 73433702
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433704
feature_type: variation
id: rs1250260533
seq_region_name: 17
source: dbSNP
start: 73433704
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433707
feature_type: variation
id: rs1424554586
seq_region_name: 17
source: dbSNP
start: 73433707
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433709
feature_type: variation
id: rs188717459
seq_region_name: 17
source: dbSNP
start: 73433709
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433710
feature_type: variation
id: rs1362860330
seq_region_name: 17
source: dbSNP
start: 73433710
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433712
feature_type: variation
id: rs1294935679
seq_region_name: 17
source: dbSNP
start: 73433712
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433713
feature_type: variation
id: rs1446778599
seq_region_name: 17
source: dbSNP
start: 73433713
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433715
feature_type: variation
id: rs141489873
seq_region_name: 17
source: dbSNP
start: 73433715
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433716
feature_type: variation
id: rs147008190
seq_region_name: 17
source: dbSNP
start: 73433716
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433717
feature_type: variation
id: rs371392188
seq_region_name: 17
source: dbSNP
start: 73433717
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433718
feature_type: variation
id: rs1037722148
seq_region_name: 17
source: dbSNP
start: 73433718
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433719
feature_type: variation
id: rs532541917
seq_region_name: 17
source: dbSNP
start: 73433719
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433720
feature_type: variation
id: rs758327345
seq_region_name: 17
source: dbSNP
start: 73433720
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433721
feature_type: variation
id: rs139075720
seq_region_name: 17
source: dbSNP
start: 73433721
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73433724
feature_type: variation
id: rs2063345213
seq_region_name: 17
source: dbSNP
start: 73433724
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73433725
feature_type: variation
id: rs748268818
seq_region_name: 17
source: dbSNP
start: 73433725
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73433726
feature_type: variation
id: rs1416194261
seq_region_name: 17
source: dbSNP
start: 73433726
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_5th_base_variant
end: 73433727
feature_type: variation
id: rs2145614898
seq_region_name: 17
source: dbSNP
start: 73433727
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_donor_region_variant
end: 73433728
feature_type: variation
id: rs118059494
seq_region_name: 17
source: dbSNP
start: 73433728
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73433734
feature_type: variation
id: rs777242180
seq_region_name: 17
source: dbSNP
start: 73433734
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433736
feature_type: variation
id: rs1218691948
seq_region_name: 17
source: dbSNP
start: 73433736
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433737
feature_type: variation
id: rs1259501703
seq_region_name: 17
source: dbSNP
start: 73433737
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433744
feature_type: variation
id: rs1309707749
seq_region_name: 17
source: dbSNP
start: 73433744
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433746
feature_type: variation
id: rs938723649
seq_region_name: 17
source: dbSNP
start: 73433746
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433747
feature_type: variation
id: rs2145614954
seq_region_name: 17
source: dbSNP
start: 73433747
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433750
feature_type: variation
id: rs2063345406
seq_region_name: 17
source: dbSNP
start: 73433750
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73433755
feature_type: variation
id: rs1251058415
seq_region_name: 17
source: dbSNP
start: 73433755
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73433756
feature_type: variation
id: rs1483800628
seq_region_name: 17
source: dbSNP
start: 73433756
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433757
feature_type: variation
id: rs749515914
seq_region_name: 17
source: dbSNP
start: 73433757
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433759
feature_type: variation
id: rs771323126
seq_region_name: 17
source: dbSNP
start: 73433759
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433760
feature_type: variation
id: rs368288903
seq_region_name: 17
source: dbSNP
start: 73433760
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433761
feature_type: variation
id: rs772493100
seq_region_name: 17
source: dbSNP
start: 73433761
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433762
feature_type: variation
id: rs892076346
seq_region_name: 17
source: dbSNP
start: 73433762
strand: 1
-
alleles:
- CCCCC
- CCCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73433766
feature_type: variation
id: rs2063345592
seq_region_name: 17
source: dbSNP
start: 73433762
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433766
feature_type: variation
id: rs142980422
seq_region_name: 17
source: dbSNP
start: 73433766
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433767
feature_type: variation
id: rs760209315
seq_region_name: 17
source: dbSNP
start: 73433767
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433769
feature_type: variation
id: rs181722149
seq_region_name: 17
source: dbSNP
start: 73433769
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433770
feature_type: variation
id: rs1599562200
seq_region_name: 17
source: dbSNP
start: 73433770
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433773
feature_type: variation
id: rs1359488687
seq_region_name: 17
source: dbSNP
start: 73433773
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433778
feature_type: variation
id: rs1001954995
seq_region_name: 17
source: dbSNP
start: 73433778
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433779
feature_type: variation
id: rs2063345756
seq_region_name: 17
source: dbSNP
start: 73433779
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433780
feature_type: variation
id: rs778292039
seq_region_name: 17
source: dbSNP
start: 73433780
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433786
feature_type: variation
id: rs1310901743
seq_region_name: 17
source: dbSNP
start: 73433786
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433788
feature_type: variation
id: rs2063345892
seq_region_name: 17
source: dbSNP
start: 73433788
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: stop_gained
end: 73433791
feature_type: variation
id: rs2145615161
seq_region_name: 17
source: dbSNP
start: 73433791
strand: 1
-
alleles:
- G
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433796
feature_type: variation
id: rs2063345936
seq_region_name: 17
source: dbSNP
start: 73433796
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433799
feature_type: variation
id: rs2145615183
seq_region_name: 17
source: dbSNP
start: 73433799
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433801
feature_type: variation
id: rs187100590
seq_region_name: 17
source: dbSNP
start: 73433801
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433802
feature_type: variation
id: rs761629975
seq_region_name: 17
source: dbSNP
start: 73433802
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433804
feature_type: variation
id: rs2063346090
seq_region_name: 17
source: dbSNP
start: 73433804
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433805
feature_type: variation
id: rs750237112
seq_region_name: 17
source: dbSNP
start: 73433805
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433807
feature_type: variation
id: rs2145615234
seq_region_name: 17
source: dbSNP
start: 73433807
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433808
feature_type: variation
id: rs756896774
seq_region_name: 17
source: dbSNP
start: 73433808
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433809
feature_type: variation
id: rs766188468
seq_region_name: 17
source: dbSNP
start: 73433809
strand: 1
-
alleles:
- T
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433810
feature_type: variation
id: rs751520516
seq_region_name: 17
source: dbSNP
start: 73433810
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433811
feature_type: variation
id: rs536792012
seq_region_name: 17
source: dbSNP
start: 73433811
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433812
feature_type: variation
id: rs142425619
seq_region_name: 17
source: dbSNP
start: 73433812
strand: 1
-
alleles:
- T
- TT
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73433813
feature_type: variation
id: rs1567770143
seq_region_name: 17
source: dbSNP
start: 73433813
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433814
feature_type: variation
id: rs373738726
seq_region_name: 17
source: dbSNP
start: 73433814
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433816
feature_type: variation
id: rs191836528
seq_region_name: 17
source: dbSNP
start: 73433816
strand: 1
-
alleles:
- GGGGG
- GGGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: frameshift_variant
end: 73433823
feature_type: variation
id: rs1213448731
seq_region_name: 17
source: dbSNP
start: 73433819
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433820
feature_type: variation
id: rs749497732
seq_region_name: 17
source: dbSNP
start: 73433820
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433821
feature_type: variation
id: rs865812602
seq_region_name: 17
source: dbSNP
start: 73433821
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433823
feature_type: variation
id: rs1485429670
seq_region_name: 17
source: dbSNP
start: 73433823
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433825
feature_type: variation
id: rs757467978
seq_region_name: 17
source: dbSNP
start: 73433825
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433835
feature_type: variation
id: rs2063346602
seq_region_name: 17
source: dbSNP
start: 73433835
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433840
feature_type: variation
id: rs1243870403
seq_region_name: 17
source: dbSNP
start: 73433840
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433842
feature_type: variation
id: rs2063346696
seq_region_name: 17
source: dbSNP
start: 73433842
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance:
- uncertain significance
consequence_type: missense_variant
end: 73433843
feature_type: variation
id: rs779304466
seq_region_name: 17
source: dbSNP
start: 73433843
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: synonymous_variant
end: 73433844
feature_type: variation
id: rs1186049014
seq_region_name: 17
source: dbSNP
start: 73433844
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433845
feature_type: variation
id: rs1421885901
seq_region_name: 17
source: dbSNP
start: 73433845
strand: 1
-
alleles:
- T
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433846
feature_type: variation
id: rs2063346833
seq_region_name: 17
source: dbSNP
start: 73433846
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: missense_variant
end: 73433847
feature_type: variation
id: rs1254752528
seq_region_name: 17
source: dbSNP
start: 73433847
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73433851
feature_type: variation
id: rs746176342
seq_region_name: 17
source: dbSNP
start: 73433851
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73433852
feature_type: variation
id: rs2063346944
seq_region_name: 17
source: dbSNP
start: 73433852
strand: 1
-
alleles:
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73433855
feature_type: variation
id: rs111614589
seq_region_name: 17
source: dbSNP
start: 73433855
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_region_variant
end: 73433856
feature_type: variation
id: rs772506253
seq_region_name: 17
source: dbSNP
start: 73433856
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73433857
feature_type: variation
id: rs1009484559
seq_region_name: 17
source: dbSNP
start: 73433857
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73433858
feature_type: variation
id: rs2063347088
seq_region_name: 17
source: dbSNP
start: 73433858
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: splice_polypyrimidine_tract_variant
end: 73433862
feature_type: variation
id: rs368441263
seq_region_name: 17
source: dbSNP
start: 73433862
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433868
feature_type: variation
id: rs2063347149
seq_region_name: 17
source: dbSNP
start: 73433865
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433866
feature_type: variation
id: rs776078195
seq_region_name: 17
source: dbSNP
start: 73433866
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433868
feature_type: variation
id: rs1374637715
seq_region_name: 17
source: dbSNP
start: 73433868
strand: 1
-
alleles:
- C
- A
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433869
feature_type: variation
id: rs747519362
seq_region_name: 17
source: dbSNP
start: 73433869
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433872
feature_type: variation
id: rs1007927489
seq_region_name: 17
source: dbSNP
start: 73433872
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433874
feature_type: variation
id: rs2063347311
seq_region_name: 17
source: dbSNP
start: 73433874
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433877
feature_type: variation
id: rs1319912201
seq_region_name: 17
source: dbSNP
start: 73433877
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433880
feature_type: variation
id: rs2063347383
seq_region_name: 17
source: dbSNP
start: 73433880
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433882
feature_type: variation
id: rs1343111324
seq_region_name: 17
source: dbSNP
start: 73433882
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433886
feature_type: variation
id: rs1015687160
seq_region_name: 17
source: dbSNP
start: 73433886
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433888
feature_type: variation
id: rs2063347481
seq_region_name: 17
source: dbSNP
start: 73433888
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433891
feature_type: variation
id: rs375597986
seq_region_name: 17
source: dbSNP
start: 73433891
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433892
feature_type: variation
id: rs2145615542
seq_region_name: 17
source: dbSNP
start: 73433892
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433893
feature_type: variation
id: rs1567770236
seq_region_name: 17
source: dbSNP
start: 73433893
strand: 1
-
alleles:
- T
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433894
feature_type: variation
id: rs2063347578
seq_region_name: 17
source: dbSNP
start: 73433894
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433895
feature_type: variation
id: rs2063347618
seq_region_name: 17
source: dbSNP
start: 73433895
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433901
feature_type: variation
id: rs2063347659
seq_region_name: 17
source: dbSNP
start: 73433901
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433909
feature_type: variation
id: rs1218714147
seq_region_name: 17
source: dbSNP
start: 73433909
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433910
feature_type: variation
id: rs1202239314
seq_region_name: 17
source: dbSNP
start: 73433910
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433913
feature_type: variation
id: rs1482339846
seq_region_name: 17
source: dbSNP
start: 73433913
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433914
feature_type: variation
id: rs2063347792
seq_region_name: 17
source: dbSNP
start: 73433914
strand: 1
-
alleles:
- GGGG
- GGG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433917
feature_type: variation
id: rs968029658
seq_region_name: 17
source: dbSNP
start: 73433914
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433915
feature_type: variation
id: rs1203786890
seq_region_name: 17
source: dbSNP
start: 73433915
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433917
feature_type: variation
id: rs1307756948
seq_region_name: 17
source: dbSNP
start: 73433917
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433918
feature_type: variation
id: rs1274672433
seq_region_name: 17
source: dbSNP
start: 73433918
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433926
feature_type: variation
id: rs1217322494
seq_region_name: 17
source: dbSNP
start: 73433926
strand: 1
-
alleles:
- A
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433929
feature_type: variation
id: rs961292929
seq_region_name: 17
source: dbSNP
start: 73433929
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433931
feature_type: variation
id: rs974397413
seq_region_name: 17
source: dbSNP
start: 73433931
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433932
feature_type: variation
id: rs558219927
seq_region_name: 17
source: dbSNP
start: 73433932
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433934
feature_type: variation
id: rs919734240
seq_region_name: 17
source: dbSNP
start: 73433934
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433936
feature_type: variation
id: rs1234396396
seq_region_name: 17
source: dbSNP
start: 73433936
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433941
feature_type: variation
id: rs1348500610
seq_region_name: 17
source: dbSNP
start: 73433941
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433942
feature_type: variation
id: rs2063348094
seq_region_name: 17
source: dbSNP
start: 73433942
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433946
feature_type: variation
id: rs1307548777
seq_region_name: 17
source: dbSNP
start: 73433946
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433947
feature_type: variation
id: rs1599562396
seq_region_name: 17
source: dbSNP
start: 73433947
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433950
feature_type: variation
id: rs1275136191
seq_region_name: 17
source: dbSNP
start: 73433950
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433952
feature_type: variation
id: rs969898846
seq_region_name: 17
source: dbSNP
start: 73433952
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433954
feature_type: variation
id: rs2063348198
seq_region_name: 17
source: dbSNP
start: 73433954
strand: 1
-
alleles:
- C
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433959
feature_type: variation
id: rs1332696331
seq_region_name: 17
source: dbSNP
start: 73433959
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433965
feature_type: variation
id: rs576487548
seq_region_name: 17
source: dbSNP
start: 73433965
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433970
feature_type: variation
id: rs2145615680
seq_region_name: 17
source: dbSNP
start: 73433970
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433971
feature_type: variation
id: rs928745156
seq_region_name: 17
source: dbSNP
start: 73433971
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433972
feature_type: variation
id: rs2063348300
seq_region_name: 17
source: dbSNP
start: 73433972
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433975
feature_type: variation
id: rs938671219
seq_region_name: 17
source: dbSNP
start: 73433975
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433979
feature_type: variation
id: rs534319878
seq_region_name: 17
source: dbSNP
start: 73433979
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433980
feature_type: variation
id: rs1567770320
seq_region_name: 17
source: dbSNP
start: 73433980
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433982
feature_type: variation
id: rs2063348382
seq_region_name: 17
source: dbSNP
start: 73433982
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433988
feature_type: variation
id: rs1471926161
seq_region_name: 17
source: dbSNP
start: 73433988
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433989
feature_type: variation
id: rs2063348423
seq_region_name: 17
source: dbSNP
start: 73433989
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433991
feature_type: variation
id: rs2063348447
seq_region_name: 17
source: dbSNP
start: 73433991
strand: 1
-
alleles:
- G
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73433994
feature_type: variation
id: rs1180912948
seq_region_name: 17
source: dbSNP
start: 73433994
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434003
feature_type: variation
id: rs2145615751
seq_region_name: 17
source: dbSNP
start: 73434003
strand: 1
-
alleles:
- "-"
- TG
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434008
feature_type: variation
id: rs2063348503
seq_region_name: 17
source: dbSNP
start: 73434009
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434009
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-
alleles:
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-
alleles:
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-
alleles:
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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assembly_name: GRCh38
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strand: 1
-
alleles:
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
source: dbSNP
start: 73434047
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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start: 73434056
strand: 1
-
alleles:
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assembly_name: GRCh38
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seq_region_name: 17
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strand: 1
-
alleles:
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assembly_name: GRCh38
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feature_type: variation
id: rs1049494341
seq_region_name: 17
source: dbSNP
start: 73434064
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
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seq_region_name: 17
source: dbSNP
start: 73434066
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs561353667
seq_region_name: 17
source: dbSNP
start: 73434069
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1415561172
seq_region_name: 17
source: dbSNP
start: 73434072
strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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feature_type: variation
id: rs2063348881
seq_region_name: 17
source: dbSNP
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strand: 1
-
alleles:
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assembly_name: GRCh38
clinical_significance: []
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id: rs2063348898
seq_region_name: 17
source: dbSNP
start: 73434076
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434077
feature_type: variation
id: rs2063348920
seq_region_name: 17
source: dbSNP
start: 73434077
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs1301091527
seq_region_name: 17
source: dbSNP
start: 73434088
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063348957
seq_region_name: 17
source: dbSNP
start: 73434089
strand: 1
-
alleles:
- T
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063348976
seq_region_name: 17
source: dbSNP
start: 73434091
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
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feature_type: variation
id: rs2063349000
seq_region_name: 17
source: dbSNP
start: 73434092
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434093
feature_type: variation
id: rs2063349019
seq_region_name: 17
source: dbSNP
start: 73434093
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434095
feature_type: variation
id: rs1474630665
seq_region_name: 17
source: dbSNP
start: 73434095
strand: 1
-
alleles:
- A
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434096
feature_type: variation
id: rs890852369
seq_region_name: 17
source: dbSNP
start: 73434096
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434097
feature_type: variation
id: rs920199944
seq_region_name: 17
source: dbSNP
start: 73434097
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434099
feature_type: variation
id: rs930283222
seq_region_name: 17
source: dbSNP
start: 73434099
strand: 1
-
alleles:
- C
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434102
feature_type: variation
id: rs2063349144
seq_region_name: 17
source: dbSNP
start: 73434102
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434105
feature_type: variation
id: rs2063349169
seq_region_name: 17
source: dbSNP
start: 73434105
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434114
feature_type: variation
id: rs1451118558
seq_region_name: 17
source: dbSNP
start: 73434114
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434115
feature_type: variation
id: rs984438987
seq_region_name: 17
source: dbSNP
start: 73434115
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434116
feature_type: variation
id: rs2063349240
seq_region_name: 17
source: dbSNP
start: 73434116
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434117
feature_type: variation
id: rs1160486698
seq_region_name: 17
source: dbSNP
start: 73434117
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434119
feature_type: variation
id: rs1421330187
seq_region_name: 17
source: dbSNP
start: 73434119
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434121
feature_type: variation
id: rs2063349311
seq_region_name: 17
source: dbSNP
start: 73434121
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434123
feature_type: variation
id: rs1007997538
seq_region_name: 17
source: dbSNP
start: 73434123
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434124
feature_type: variation
id: rs1015217581
seq_region_name: 17
source: dbSNP
start: 73434124
strand: 1
-
alleles:
- G
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434126
feature_type: variation
id: rs576578941
seq_region_name: 17
source: dbSNP
start: 73434126
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434127
feature_type: variation
id: rs1243341052
seq_region_name: 17
source: dbSNP
start: 73434127
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434128
feature_type: variation
id: rs896820171
seq_region_name: 17
source: dbSNP
start: 73434128
strand: 1
-
alleles:
- G
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assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434135
feature_type: variation
id: rs1415953002
seq_region_name: 17
source: dbSNP
start: 73434135
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434140
feature_type: variation
id: rs995426739
seq_region_name: 17
source: dbSNP
start: 73434140
strand: 1
-
alleles:
- CCCC
- CCC
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434143
feature_type: variation
id: rs1463364704
seq_region_name: 17
source: dbSNP
start: 73434140
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434141
feature_type: variation
id: rs543975403
seq_region_name: 17
source: dbSNP
start: 73434141
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434142
feature_type: variation
id: rs945233365
seq_region_name: 17
source: dbSNP
start: 73434142
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434146
feature_type: variation
id: rs2145616106
seq_region_name: 17
source: dbSNP
start: 73434146
strand: 1
-
alleles:
- A
- "-"
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434147
feature_type: variation
id: rs1042281595
seq_region_name: 17
source: dbSNP
start: 73434147
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434148
feature_type: variation
id: rs1027355304
seq_region_name: 17
source: dbSNP
start: 73434148
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434149
feature_type: variation
id: rs2063349646
seq_region_name: 17
source: dbSNP
start: 73434149
strand: 1
-
alleles:
- C
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434156
feature_type: variation
id: rs969845006
seq_region_name: 17
source: dbSNP
start: 73434156
strand: 1
-
alleles:
- T
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434159
feature_type: variation
id: rs903793010
seq_region_name: 17
source: dbSNP
start: 73434159
strand: 1
-
alleles:
- C
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434164
feature_type: variation
id: rs1201942420
seq_region_name: 17
source: dbSNP
start: 73434164
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434172
feature_type: variation
id: rs184124603
seq_region_name: 17
source: dbSNP
start: 73434172
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434173
feature_type: variation
id: rs2063349758
seq_region_name: 17
source: dbSNP
start: 73434173
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434176
feature_type: variation
id: rs1317412333
seq_region_name: 17
source: dbSNP
start: 73434176
strand: 1
-
alleles:
- G
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434179
feature_type: variation
id: rs1433097230
seq_region_name: 17
source: dbSNP
start: 73434179
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434181
feature_type: variation
id: rs2145616172
seq_region_name: 17
source: dbSNP
start: 73434181
strand: 1
-
alleles:
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434182
feature_type: variation
id: rs2063349824
seq_region_name: 17
source: dbSNP
start: 73434182
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434186
feature_type: variation
id: rs1289777841
seq_region_name: 17
source: dbSNP
start: 73434186
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434187
feature_type: variation
id: rs2063349866
seq_region_name: 17
source: dbSNP
start: 73434187
strand: 1
-
alleles:
- A
- G
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434189
feature_type: variation
id: rs79403938
seq_region_name: 17
source: dbSNP
start: 73434189
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434191
feature_type: variation
id: rs1237071400
seq_region_name: 17
source: dbSNP
start: 73434191
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434196
feature_type: variation
id: rs1285059689
seq_region_name: 17
source: dbSNP
start: 73434196
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434199
feature_type: variation
id: rs960074909
seq_region_name: 17
source: dbSNP
start: 73434199
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434202
feature_type: variation
id: rs2145616219
seq_region_name: 17
source: dbSNP
start: 73434202
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434204
feature_type: variation
id: rs2063349983
seq_region_name: 17
source: dbSNP
start: 73434204
strand: 1
-
alleles:
- A
- C
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434205
feature_type: variation
id: rs2063350003
seq_region_name: 17
source: dbSNP
start: 73434205
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434208
feature_type: variation
id: rs889823820
seq_region_name: 17
source: dbSNP
start: 73434208
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434211
feature_type: variation
id: rs1423448536
seq_region_name: 17
source: dbSNP
start: 73434211
strand: 1
-
alleles:
- TT
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434217
feature_type: variation
id: rs2063350036
seq_region_name: 17
source: dbSNP
start: 73434216
strand: 1
-
alleles:
- C
- T
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434218
feature_type: variation
id: rs2063350050
seq_region_name: 17
source: dbSNP
start: 73434218
strand: 1
-
alleles:
- AAAA
- AAA
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434224
feature_type: variation
id: rs2063350073
seq_region_name: 17
source: dbSNP
start: 73434221
strand: 1
-
alleles:
- G
- A
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434225
feature_type: variation
id: rs201000754
seq_region_name: 17
source: dbSNP
start: 73434225
strand: 1
-
alleles:
- A
- G
assembly_name: GRCh38
clinical_significance: []
consequence_type: intron_variant
end: 73434230
feature_type: variation
id: rs2063350124
seq_region_name: 17
source: dbSNP
start: 73434230
strand: 1
-
alleles:
- "-"